Predation on different-sized quail eggs in an artificial-nest study in western Newfoundland

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.

1999 ◽  
Vol 29 (12) ◽  
pp. 1900-1910 ◽  
Author(s):  
Susan E Cotterill ◽  
Susan J Hannon

We examined whether nest predation in unharvested blocks of trembling aspen (Populus tremuloides Michx.) would increase when adjacent stands were clearcut in the boreal mixedwood forest of Alberta, in 1993, 1994, and 1998. Artificial nests placed on the ground and in shrubs were baited with Chinese painted quail (Coturnix chinensis L.) and plasticine eggs, which along with cameras, were used to identify nest predators. Fragmented sites were isolated from continuous forest by clear-cutting in 1994, while control sites remained unfragmented. Overall, predation on ground and shrub nests did not increase in isolated forest patches post-harvest (p = 0.056 and p = 0.085, respectively), nor was there a consistent effect of distance from a clearcut edge (p >= 0.050). Predation on ground nests was higher in 1994 and 1998 compared with 1993 levels (p < 0.001), while predation on shrub nests remained relatively constant over the 3 years (p >= 0.073). Mice, voles, and red squirrels (Tamiasciurus hudsonicus Erxleben) were the main identified predators of ground and shrub nests, respectively. Probability of nest predation could not be consistently predicted by nest site vegetation or adjacent land cover, but was related to predator abundance. However, neither predators nor songbirds congregate at recent clearcut-forest edges, and we conclude that elevated nest predation caused by clear-cutting may not occur in the boreal mixedwood, at least not at current levels of harvest and within 5 years of clear-cutting.


The Condor ◽  
2006 ◽  
Vol 108 (1) ◽  
pp. 232-238 ◽  
Author(s):  
Adam M. Siepielski

Abstract Nest predation is thought to play an important role in structuring certain breeding bird communities. One potential consequence of nest predation is lower recruitment in breeding birds, which may be manifested as lower breeding bird abundance. Lodgepole pine (Pinus contorta ssp. latifolia) forests east and west of the Rocky Mountains became isolated following glacial retreat 12 000 years ago and differ in whether or not red squirrels (Tamiasciurus hudsonicus), which are a key nest predator, are present. Breeding bird abundance in lodgepole pine forests was compared between four ranges with red squirrels and four ranges without red squirrels. Species grouped into canopy and understory nesting guilds were, on average, two and three times more abundant, respectively, in forest ranges without red squirrels than in ranges with red squirrels; no statistically significant differences were found for midstory, ground, or cavity nesters. These results suggest that geographic variation in the presence or absence of red squirrels is likely important in structuring breeding bird communities in lodgepole pine forests across the landscape.


2002 ◽  
Vol 29 (4) ◽  
pp. 341 ◽  
Author(s):  
Lainie Berry

Predation rates of nests at human-induced habitat edges may be greater than in forest interior due to differences in predator assemblages and predator activity. I compared the predation rates on 192 artificial nests containing plasticine eggs placed in forest edge and interior sites at Bunyip State Park, Victoria. The nest-predation rates at the forest edge sites were significantly greater (mean = 52–58%) than that at the forest interior sites (mean = 30–39%). The relative rates of predation by birds compared with mammals were significantly greater at forest edge sites (mean = 78–94%) than at forest interior sites (mean = 36–67%). Higher rates of nest predation at forest edges appeared to be due to greater densities of avian predators such as the grey shrike-thrush (Colluricincla harmonica), and/or lower abundances of small mammals. However, biases towards certain predator types may mask real, or create false, patterns in predation rates of artificial nests. A better understanding of how predators respond to artificial nests compared with natural nests is required. Until then, results of predation studies that use artificial nests should be interpreted with caution.


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.


2014 ◽  
Vol 44 (3) ◽  
pp. 393-396 ◽  
Author(s):  
Fernanda Michalski ◽  
Darren Norris

Observational and experimental studies have shown that increased concealment of bird nests reduces nest predation rates. The objective of the present study was to evaluate differences in predation rates between two experimental manipulations of artificial ground nests (i.e., clearing an area around the artificial nest or leaving it as natural as possible), and test whether environmental variables also affected nest predation in an undisturbed area of Amazonian forest in eastern Brazil. A generalized linear model was used to examine the influence of five variables (manipulation type, perpendicular distance from the main trail, total basal area of trees surrounding the nest site, understorey density, and liana quantity) on nest predation rates. Model results, showed that manipulation type was the only variable that significantly affected nest predation rates. Thus, to avoid systematic biases, the influence of nest site manipulation must be taken into consideration when conducting experiments with artificial nests.


The Condor ◽  
2000 ◽  
Vol 102 (4) ◽  
pp. 838-847 ◽  
Author(s):  
Jukka Jokimäki ◽  
Esa Huhta

Abstract We studied nest predation pressure on birds along an urban gradient in urban parks in three Finnish towns. Artificial ground nests with Japanese Quail (Coturnix coturnix japonicus) eggs were depredated more in the urban area than in the adjacent forest area. Within each town, the nest predation rate was higher in the town center than in the less urbanized area of detached houses. Predation rates did not vary from year to year or between study towns. Abundances of generalist avian predators were higher in the town center than in the area of detached houses and in the surrounding forest area. Most of the nests in the town center were destroyed by avian predators. Predation rate of artificial nests in each of the town areas was higher in managed parks than in unmanaged parks, presumably due to the less dense vegetation in the managed than the unmanaged parks. A test involving covering nests revealed that artificial nests covered by adjacent vegetation survived better than nests with less cover. In our study, artificial nest loss reflected the distribution of avian nest predators. Ground nesters were present at lower abundances in areas where concealing vegetation was missing and avian nest predation was high. Apparently, nest predation is one of the several possible mechanism affecting urban bird assemblages.


The Auk ◽  
2000 ◽  
Vol 117 (1) ◽  
pp. 136-146 ◽  
Author(s):  
Sheila A. Rangen ◽  
Robert G. Clark ◽  
Keith A. Hobson

Abstract Artificial nests are commonly used to investigate relative rates of nest predation in birds, but several methodological considerations need to be addressed before results from natural and artificial nests can be compared. Using field and laboratory experiments, we examined responses of predators to visual and olfactory cues that were associated with wicker nests and their contents. Avian predators did not discriminate between wicker nests dipped in mud and those covered by a camouflage fabric, whereas mammalian predators showed a weak tendency to depredate camouflaged nests. Nests containing plasticine eggs were depredated more often than nests containing only quail eggs and finch eggs, although no response to number of plasticine eggs in nests was found. The higher predation of nests with plasticine eggs may have resulted because small mammals, relying on olfactory cues, comprised a large portion of the predator assemblage. Field results were supported in tests where captive deer mice (Peromyscus maniculatus) were attracted to assortments of egg types that included plasticine. Time required by captive deer mice to penetrate quail eggs and finch eggs versus plasticine eggs varied as a function of egg size and shell thickness and strength. Overall, domestic finch eggs provided a better alternative to quail eggs because they were small enough to allow detection of predation events by small mammals and did not have an unnatural odor like plasticine. Potential problems with nest concealment, egg visibility, egg odors, and other factors must be resolved to enhance the design and reliability of artificial nest experiments.


2005 ◽  
Vol 32 (4) ◽  
pp. 313 ◽  
Author(s):  
Fiona J. Fraser ◽  
Peter J. Whitehead

Depredation of artificial ground nests was examined in tropical savanna in northern Australia to assess potential predation pressures on nests of the partridge pigeon (Geophaps smithii), a declining tropical granivore. Predation rates were examined at two sites, Kakadu National Park (which supported a relatively high density of partridge pigeons) and Berry Springs (which had greater habitat fragmentation and comparatively low partridge pigeon density). The effects of distance from road, understorey structure, topography and nest-microsite concealment on nest predation rates were examined. Artificial-nest predation rates were greater at 150 m from roads than <1 m from the roadside. Predation rates did not vary with understorey structure, topography, or level of nest concealment. There was marked variation between sites, with predation levels at Kakadu more than double those recorded for Berry Springs. Discerning predator identity, or even the size of a predator, from marks left in clay eggs proved difficult and was possible for ~35% of predation events. Of these, 42% of predation events involved predators of a size we considered too small to take a natural partridge pigeon nest. We suggest that extrapolation from artificial to natural ground-nest predation rates be undertaken with caution for landscapes such as Australia’s tropical savanna, which supports a high diversity and abundance of small potential predators of artificial nests. There was no evidence of predation by birds, and the methodology proved inadequate for identifying predation by feral cats (Felis catus).


2003 ◽  
Vol 33 (5) ◽  
pp. 922-930 ◽  
Author(s):  
Marylène Boulet ◽  
Marcel Darveau ◽  
Louis Bélanger

The black spruce (Picea mariana (Mill.) BSP) forests of Quebec are often harvested according to a single-pass system where clearcuts are separated by 20- to 60-m-wide forest strips. Little is known about the suitability of these strips as habitats for breeding birds. We selected five nonriparian strips, five riparian strips, and five forest control sites located in a forested area of central Quebec. During 1997–1998, we monitored the predation of artificial bird nests baited with a common quail (Coturnix coturnix L.) egg and a plasticine egg and the breeding activity of adult songbirds in strips and controls. Artificial nest predation was high in all sites (72%). The most common predators were specialists of mature coniferous forests: gray jays (Perisoreus canadensis L.) and red squirrels (Tamiasciurus hudsonicus Erxleben). In forest-dwelling bird species, the number of breeding pairs was lower in strips than in controls. We conclude that the small number of forest-dwelling breeding birds observed in strips is not related to an increase in predation pressure following harvest of adjacent forests and that forest strips are not suitable breeding habitats for these species.


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