Is the risk of nest predation heterospecifically density-dependent in precocial species belonging to different nesting guilds?

2011 ◽  
Vol 89 (12) ◽  
pp. 1164-1171 ◽  
Author(s):  
Johan Elmberg ◽  
Hannu Pöysä

Nest predation is a key source of mortality and variation in fitness, but the effect co-occurring species belonging to different nesting guilds have on each other’s nest success is poorly understood. By using artificial nests, we tested if predation on cavity nests of Common Goldeneyes ( Bucephala clangula (L., 1758)) is increased in the presence of ground nests of Mallards ( Anas platyrhynchos L., 1758) and vice versa. Specifically, by adding ground nests in the vicinity of cavity nests, we tested the hypothesis that predation on cavity nests is heterospecifically density-dependent. A shared predator, the pine marten ( Martes martes (L., 1758)), was intensively hunted in one of the study areas, but not in the other, leading to most individuals in the former being naïve immigrants. Cavity-nest fate was not affected by addition of ground nests. Similarly, ground-nest survival did not decrease when nearby cavity nests were depredated. Fate of nests in a given nest cavity was highly predictable between years in the study area with minimal removal of pine martens, but not in the one with intensive removal. Predation rate was higher on cavity nests than on ground nests. Predation on ground nests was lower in the study area with intensive removal of pine martens. We conclude there was neither apparent competition between guilds nor heterospecific density-dependence in predation risk.

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.


The Condor ◽  
2002 ◽  
Vol 104 (3) ◽  
pp. 496-506 ◽  
Author(s):  
W. Matthew Vander Haegen ◽  
Michael A. Schroeder ◽  
Richard M. DeGraaf

Abstract Clearing of shrubsteppe communities for agriculture has created a highly fragmented landscape in eastern Washington, a condition that has been shown to adversely affect nesting success of birds in some forest and grassland communities. We used artificial nests monitored by cameras to examine relative effects of fragmentation, distance to edge, and vegetation cover on nest predation rates and to identify predators of shrubsteppe-nesting passerines and grouse. Predation rate for artificial nests was 26% (n = 118). Fragmentation had a strong influence on predation rates for artificial nests, with nests in fragmented landscapes about 9 times more likely to be depredated as those in continuous landscapes. Daily survival rate (± SE) for 207 real nests of 4 passerine species also was greater in continuous (0.978 ± 0.004) than in fragmented (0.962 ± 0.006) landscapes, although pattern of predation between real and artificial nests was not consistent among sites. Artificial nests were depredated by Common Ravens (Corvus corax), Black-billed Magpies (Pica hudsonia), Sage Thrashers (Oreoscoptes montanus), least chipmunks (Tamias minimus), and mice. Most nests in fragments were depredated by corvids (58%), whereas only Sage Thrashers and small mammals depredated nests in continuous landscapes. Increased predation by corvids and lower nest success in fragmented landscapes may have played a part in recent declines of some shrubsteppe birds. Future research should measure annual reproductive success of individual females and survival rates of juveniles and adults. Depredación de Nidos Naturales y Artificiales en Paisajes de Estepa Arbustiva Fragmentados por Agricultura Resumen. El reemplazo de estepa arbustiva por campos de cultivo ha creado un paisaje altamente fragmentado en el este de Washington, afectando adversamente el éxito de nidificación de aves en algunas comunidades de bosque y pastizal. Usamos nidos artificiales monitoreados por cámaras para examinar los efectos relativos de la fragmentación, la distancia al borde y la cobertura de la vegetación sobre las tasas de depredación de nidos, y para identificar los depredadores de paserinos y gallinas silvestres (Phasianidae) que nidifican en la estepa arbustiva. La tasa de depredación de los nidos artificiales fue del 26% (n = 118). La fragmentación tuvo una fuerte influencia en las tasas de depredación de nidos artificiales, ya que los nidos en paisajes fragmentados tuvieron una probabilidad de ser depredados 9 veces mayor que aquellos en paisajes continuos. La tasa de supervivencia diaria (± EE) de 207 nidos naturales pertenecientes a 4 especies de paserinos también fue mayor en paisajes continuos (0.978 ± 0.004) que fragmentados (0.962 ± 0.006), aunque el patrón de depredación entre nidos naturales y artificiales no fue consistente entre sitios. Los nidos artificiales fueron depredados por Corvus corax, Pica hudsonia, Oreoscoptes montanus, Tamias minimus y ratones. La mayoría de los nidos en fragmentos fueron depredados por C. corax (58%), mientras que sólo O. montanus y pequeños mamíferos depredaron nidos en paisajes continuos. Un incremento en la depredación por parte de C. corax y un menor éxito de los nidos en paisajes fragmentados puede haber jugado un rol en la disminución de algunas aves de la estepa arbustiva. Futuras investigaciones deberían medir el éxito reproductivo anual de hembras individuales y las tasas de supervivencia de juveniles y adultos.


1992 ◽  
Vol 70 (12) ◽  
pp. 2498-2500 ◽  
Author(s):  
Leonard Reitsma

Experiments using artificial nests to test whether predation varies with nest density were conducted in a northern hardwood forest in New Hampshire in June 1989. Nests were baited with quail eggs and placed at densities similar to and substantially higher than the range of natural nest densities. There was no statistically significant difference in predation levels among densities, but there was a trend for higher predation at the highest density.


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.


1999 ◽  
Vol 29 (12) ◽  
pp. 1911-1915 ◽  
Author(s):  
J Douglas Steventon ◽  
Peter K Ott ◽  
Kenneth L MacKenzie

Based on relative abundance data, partial cutting has been suggested as a technique to maintain habitat for birds associated with late-seral forests, but there has been little study of partial cutting effects on nesting success. One of the primary limitations to nesting success is nest predation. We compared predation rates (proportion of nests disturbed in a 14-day period) in partially cut (30 or 60% basal area removal), clearcut, and uncut forests in northwestern British Columbia, in two experiments using ground-placed (1993) and shrub-placed (1998) artificial nests. In the ground-nest experiment there was a very low predation rate (0.06) and no detectable difference among treatments (p = 0.403). In the shrub-nest experiment, there was a 0.36 predation rate and little evidence of treatment differences (p = 0.295). Based on 90% confidence intervals for differences in observed predation rate, the 30% removal clearly did not increase predation risk relative to uncut forest. With the 60% removal, however, we cannot rule out a possible increase in predation risk compared with either uncut forest or clearcuts.


2006 ◽  
Vol 16 (4) ◽  
pp. 309-316 ◽  
Author(s):  
JENŐ J. PURGER ◽  
LÍDIA A. MÉSZÁROS

To investigate whether nest predation can influence the breeding success of Ferruginous Ducks Aythya nyroca, artificial nests were used in Nagyberek, the strictly protected swamp pond of the Juniper Woodland Nature Conservation Area (Somogy county, south Hungary). Experimentation lasted for 4 weeks, a similar length of time to the incubation period of Ferruginous Ducks. After 1 week, 80% of nests were intact, after 2 weeks only 46%, and after 3 and 4 weeks only 2% remained undamaged. Nest survival rates were not affected by the width of the sedge stands, but as water levels surrounding nests decreased, nests became more accessible to Wild Boar Sus scrofa and other land mammal predators, which increased the rate of predation. Artificially maintaining water levels would not only decrease the predation rate of nests, but would also maintain feeding areas for ducks. Wild Boar were the main cause of clutch loss in this area, and therefore by management measures, such as a reduction in their abundance or attracting them away from potential nesting sites by providing food elsewhere, the breeding success of the Ferruginous Ducks may be further improved.


2007 ◽  
Vol 121 (2) ◽  
pp. 150
Author(s):  
Vanessa B. Harriman ◽  
Justin A. Pitt ◽  
Serge Larivière

Ground-nesting birds typically experience high predation rates on their nests, often by mammalian predators. As such, researchers and wildlife managers have employed numerous techniques to mitigate nest predation. We investigated the use of scents as repellents to deter predators from both artificial and natural ground nests. Survival rates of artificial nests did not differ among six groups of substances (Wald ?2 df = 5 = 4.53, P < 0.48); however the chronology of predation among groups differed. A commercial Coyote urine based deterrent (DEER-D-TERTM), human hair, and Worcestershire sauce were depredated faster than the control (F4,5 = 40.3, P < 0.001). Nest survival of natural nests differed among those groups tested (Wald ?2 df = 2 = 11.8, P < 0.005); the eight mothball treatment decreased survival (Wald ?2 df = 1 = 11.5, P < 0.005), which indicated that novel smells may attract predators or result in duck nest abandonment when coupled with natural duck scent. Chronologies of predation events among treatment groups were not different for natural nests (F2,3 = 1.9, P = 0.22). These findings indicate an interaction between novel scents and predator olfactory cues.


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.


2005 ◽  
Vol 32 (4) ◽  
pp. 320-325 ◽  
Author(s):  
HOLLY P. JONES ◽  
R. WILLIAMHENRY ◽  
GREGG R. HOWALD ◽  
BERNIE R. TERSHY ◽  
DONALD A. CROLL

Introduced rats depredate every life stage of island nesting seabirds, but the extent of predation is rarely quantified. Introduced black rat (Rattus rattus) and native deer mouse (Peromyscus maniculatus anacapae) predation on Xantus's murrelet (Synthliboramphus hypoleucus scrippsi) nests was experimentally quantified using artificial nests before and after rat eradication on Anacapa Island (California). The staged rat eradication programme provided experimental treatments: in 2002 rats were eradicated on one island (East Anacapa Islet) and remained on two islands (Middle and West Anacapa Islets), providing a control comparison, and, in 2003, rats were eradicated from the remaining islands (Middle and West Anacapa Islets). In 2002, 96% of artificial nests were depredated on control islands (rats present) with rats accounting for most predation. Nest predation on the treatment island (rats eradicated) in 2002 was significantly lower: 8% of artificial nests were depredated, mostly by endemic deer mice. In 2003, following rat eradication on the remaining islands (Middle and West Anacapa Islets), nest predation was reduced from 96% in 2002 to 3% of total nests in 2003. Predation of nests on East Anacapa Islet (rats eradicated in 2002) increased significantly due to reintroduction and recovery of native deer mouse populations, with 23% of artificial nests depredated. The inference is that rat predation on real Xantus's murrelet nests was responsible for the historically low nesting success and small population sizes of breeding murrelets on Anacapa Island. With rats removed, the hatching success of Xantus's murrelet chicks and the number of individuals nesting on Anacapa Island will increase dramatically. Artificial nest studies are particularly well suited to quantifying introduced rat impacts on hole and crevice nesting seabirds and can simultaneously serve as an effective monitoring tool to detect the presence of rats and the recovery of native nest predators.


The Auk ◽  
2006 ◽  
Vol 123 (1) ◽  
pp. 82-96
Author(s):  
Brady J. Mattsson ◽  
Gerald J. Niemi

Abstract Microsite, patch, and landscape conditions may interact to influence nest predation. In northern Minnesota, silvicultural and agricultural practices may be involved in recent increases in nest predators and regional declines in several ground-nesting songbirds. To examine this problem, we evaluated 17 hierarchical models of predation on Ovenbird (Seiurus aurocapilla) nests that included microsite variables, distances to edges, and amount of core forest within a 2-km radius surrounding six study plots. During 2000 and 2001, 157 Ovenbird nests were monitored to estimate nest predation rates. A model that included the main effects of litter depth and core forest area and an interaction term between the two best described variation in predation on Ovenbird nests (AICc weight = 0.83). The nest predation rate from this model was 0.51 ± 0.01 (mean ± SE), assuming mean values of litter depth and amount of core forest. Shallow litter was associated with higher nest predation in three plots surrounded by less core habitat (40–60 ha), whereas there was no relationship in three plots surrounded by more core area (100–150 ha). Management that promotes deep leaf litter and the maintenance of large, intact forest tracts will likely benefit Ovenbirds and other forest songbirds. Factores que Influencian la Depredación de Nidos de Seiurus aurocapilla en los Bosques del Norte: Interacciones a través de las Escalas Espaciales


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