scholarly journals Nestling begging calls increase predation risk by corvids

2019 ◽  
Vol 69 (2) ◽  
pp. 137-155
Author(s):  
Magne Husby
Keyword(s):  
Nest Predation ◽  
Predation Rate ◽  
Artificial Nest ◽  
Auditory Cues ◽  
Artificial Nests ◽  
Breeding Failure ◽  
Nestling Begging ◽  
Real Costs ◽  
Insight Into ◽  
Nest Predators

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.

scholarly journals Artificial Nest Predation and Abundance of Birds Along an Urban Gradient

The Condor ◽  
2000 ◽  
Vol 102 (4) ◽  
pp. 838-847 ◽  
Author(s):  
Jukka Jokimäki ◽  
Esa Huhta
Keyword(s):  
Nest Predation ◽  
Predation Rate ◽  
Forest Area ◽  
Urban Gradient ◽  
Artificial Nest ◽  
Artificial Nests ◽  
Avian Predators ◽  
Avian Nest ◽  
Town Center ◽  
The Town

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.

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
Keyword(s):  
Japanese Quail ◽  
Small Mammals ◽  
Nest Predation ◽  
Egg Size ◽  
Tamiasciurus Hudsonicus ◽  
Buffer Strips ◽  
Artificial Nest ◽  
Red Squirrels ◽  
Artificial Nests ◽  
Riparian Buffer Strips

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.

scholarly journals Predation on Real and Artificial Nests in Shrubsteppe Landscapes Fragmented by Agriculture

The Condor ◽  
2002 ◽  
Vol 104 (3) ◽  
pp. 496-506 ◽  
Author(s):  
W. Matthew Vander Haegen ◽  
Michael A. Schroeder ◽  
Richard M. DeGraaf
Keyword(s):  
Nest Predation ◽  
Survival Rates ◽  
Predation Rate ◽  
Future Research ◽  
Fragmented Landscape ◽  
Corvus Corax ◽  
Artificial Nests ◽  
Fragmented Landscapes ◽  
Eastern Washington ◽  
Predation Rates

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.

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
Keyword(s):  
Nest Predation ◽  
Predation Rate ◽  
Apparent Competition ◽  
Artificial Nests ◽  
Nest Cavity ◽  
Density Dependent ◽  
Pine Martens ◽  
Cavity Nest ◽  
The One ◽  
Cavity Nests

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.

scholarly journals Macroecology of North European Wet Grassland Landscapes: Habitat Quality, Waders, Avian Predators and Nest Predation

2021 ◽  
Vol 13 (15) ◽  
pp. 8138
Author(s):  
Michael Manton ◽  
Per Angelstam
Keyword(s):  
Developmental Stage ◽  
Habitat Quality ◽  
Nest Predation ◽  
Relative Rate ◽  
Predation Pressure ◽  
Ecological Processes ◽  
Artificial Nests ◽  
Wet Grassland ◽  
Nest Loss ◽  
Nest Predators

Wet grassland degradation is a global issue that involves both altered land cover patterns and ecological processes, which affect the distribution and abundance of species. The sharp decline in European wader bird (Charadrii) populations is a good example. The aim of this study is to test the hypothesis that the anthropogenic developmental stage of wet grassland habitats and landscapes drives avian nest predator abundance, and thus the predation pressure on nests, which is a major cause of wader bird declines. Using a macroecological approach we selected six wet grassland landscapes representing a gradient in both grassland habitat development and breeding wader population status in four European countries (Belarus, Iceland, Lithuania and Sweden). We (1) mapped wader and avian predator assemblages in multiple wet grassland patches in each landscape, (2) used artificial nests to estimate the relative rate of egg predation, and (3) analyzed relationships between nest predation pressure, corvid nest predators versus raptors, nest loss and the stage of wet grassland habitat and landscape development. We found (1) inverse relationships between the abundance of corvids and waders, as well as between wet grassland developmental stage and waders, and (2) a positive correlation between the probability of nest loss and the density of corvid birds. In conclusion, we found a clear macroecological pattern linking habitat quality, wader populations, nest predators and nest predation. These linkages stress the importance of including nest predation as a factor limiting wader bird populations, and that corvid control or management may be useful management tools.

scholarly journals Artificial nest predation rates vary depending on visibility in the eastern Brazilian Amazon

2014 ◽  
Vol 44 (3) ◽  
pp. 393-396 ◽  
Author(s):  
Fernanda Michalski ◽  
Darren Norris
Keyword(s):  
Nest Predation ◽  
Generalized Linear Model ◽  
Nest Site ◽  
Experimental Studies ◽  
Basal Area ◽  
Artificial Nest ◽  
Artificial Nests ◽  
Eastern Brazil ◽  
Systematic Biases ◽  
Predation Rates

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.

Effect of partial cutting on predation risk to artificial bird nests

1999 ◽  
Vol 29 (12) ◽  
pp. 1911-1915 ◽  
Author(s):  
J Douglas Steventon ◽  
Peter K Ott ◽  
Kenneth L MacKenzie
Keyword(s):  
Predation Risk ◽  
Nest Predation ◽  
Basal Area ◽  
Predation Rate ◽  
Nesting Success ◽  
Partial Cutting ◽  
Artificial Nests ◽  
Detectable Difference ◽  
Predation Rates ◽  
Rule Out

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.

Response to logging by a limited but variable nest predator guild in the boreal forest

2008 ◽  
Vol 38 (7) ◽  
pp. 1974-1982 ◽  
Author(s):  
Randy G. Thompson ◽  
Ian G. Warkentin ◽  
Stephen P. Flemming
Keyword(s):  
Boreal Forest ◽  
Nest Predation ◽  
Forest Cover ◽  
Landscape Fragmentation ◽  
Artificial Nests ◽  
Gray Jays ◽  
Predator Guild ◽  
Nest Predator ◽  
Predation Rates ◽  
Nest Predators

Predation rates on the eggs and young of forest-nesting songbirds typically rise in association with anthropogenic fragmentation, but predator responses depend on the spatial scale of disturbance, context, and predator assemblages present. For landscapes that are naturally fragmented, such as the boreal forest, our understanding of nest predation patterns associated with harvest may be further confounded by an additive response of nest predators to the loss of forest cover and the extension of habitat edges. We examined predation rates on artificial nests across a range of values for landscape metrics reflecting natural and anthropogenic forest fragmentation during two summers in boreal forest stands of western Newfoundland, Canada. Nest predation by gray jays ( Perisoreus canadensis (L.)) increased significantly in logged areas, and gray jay abundance was positively linked to increasing amounts of logged edge; however, there was no response to the extent of natural openings suggesting that nest predation by jays was additive in the presence of harvest-created openings. In contrast, neither mammalian nest predators nor the unidentified predators (responsible for the largest proportion of nest losses) showed any association with the landscape fragmentation metrics assessed. Year effects shown by the unidentified nest predator category did coincide with a marked increase in small mammal and Newfoundland marten ( Martes americana (Turton) subsp. atrata (Bangs)) populations during our study. Thus, we were able to identify an additive predation response to logging, but also that the activities of predators may vary over space and time and, in turn, may variably influence the success of songbirds nesting in forests fragmented by logging.

scholarly journals Possible effects of nest predation on the breeding success of Ferruginous Ducks Aythya nyroca

2006 ◽  
Vol 16 (4) ◽  
pp. 309-316 ◽  
Author(s):  
JENŐ J. PURGER ◽  
LÍDIA A. MÉSZÁROS
Keyword(s):  
Wild Boar ◽  
Breeding Success ◽  
Nest Predation ◽  
Survival Rates ◽  
Predation Rate ◽  
Water Levels ◽  
Conservation Area ◽  
Artificial Nests ◽  
Management Measures ◽  
Nesting Sites

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.

Predation of artificial ground nests in Australian tropical savannas: inverse edge effects

2005 ◽  
Vol 32 (4) ◽  
pp. 313 ◽  
Author(s):  
Fiona J. Fraser ◽  
Peter J. Whitehead
Keyword(s):  
Nest Predation ◽  
National Park ◽  
Tropical Savanna ◽  
Northern Australia ◽  
Artificial Nest ◽  
Tropical Savannas ◽  
Artificial Nests ◽  
Predator Identity ◽  
High Diversity ◽  
Predation Rates

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).

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