scholarly journals Do Repugnant Scents Increase Survival of Ground Nests? A Test with Artificial and Natural Duck Nests

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.

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.


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.


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.


2016 ◽  
Vol 15 (2) ◽  
pp. 137 ◽  
Author(s):  
Melina Soledad Simoncini ◽  
María Virginia Parachú Marcó ◽  
Thiago Costa Gonçalves Portelinha ◽  
Carlos Ignacio Piña

Predation is a major cause of crocodilian egg loss. However, at present, the mechanisms by which predators detect nests is unknown. Previous studies have reported that predators are able to detect prey using both visual and olfactory cues. This study aims to determine the natural predation rate on Broad-snouted Caiman (Caiman latirostris) nests in a “normal” year (i.e., no extreme climatic events) and whether olfactory or visual cues attract predators to caiman nests, and to evaluate the effect of maternal presence on nest predation. In December 2010, we searched for nests in the north of Santa Fe Province, Argentina. Each nest was assigned to one of the following treatments: (1) control nests (nests were observed from a distance to avoid disturbance), (2) visual attraction nests (yellow flagging tapes were tied to vegetation around the nest), (3) olfactory attraction nests (nests were opened, one egg from the clutch was broken, and then the nests were covered again), (4) olfactory attraction from human disturbance (material was manipulated by researchers). The natural predation rate on broad-snouted caiman nests was found to be 21% during the nesting season. Both olfactory and visual cues were associated with increased predation rates, and human disturbance was strongly associated with increased nest predation at terrestrial sites. Predation rates were less at nests attended by female caiman. Management programs that harvest eggs in wild populations (ranching) are predicated on the assumption that removal of some eggs is sustainable, because some will be lost to natural causes (e.g., predation and flooding) and the remaining hatchlings will have improved survival rates. To reduce nest predation of Broad-snouted Caiman between the time when the nest is found and when the eggs are collected, we propose to avoid identification of nest sites with highly visible markings (e.g., flagging tapes tied to vegetation around nests) and to collect eggs immediately after they are found


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.


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.


2008 ◽  
Vol 38 (7) ◽  
pp. 1974-1982 ◽  
Author(s):  
Randy G. Thompson ◽  
Ian G. Warkentin ◽  
Stephen P. Flemming

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.


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.


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).


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