avian predation
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2021 ◽  
Author(s):  
◽  
Brittany Florence-Bennett

<p>Wildlife management is fraught with challenges due to the complexities of community ecology. Interventions aimed at restoring ecosystems, or managing species, can have unintended negative outcomes for target species. The effect of avian predation on native lizard fauna in New Zealand is not clearly understood, despite birds being regarded as top predators within mammal-free ecosystems. At least thirty-one species of bird have been recorded preying on native lizards, but few studies have directly addressed avian predation on lizards, with the majority of evidence sourced from published anecdotes. New Zealand’s herpetofauna are already vulnerable due to range contractions resulting from mammalian predation and habitat loss, with 87% of New Zealand lizard species considered ‘At Risk’ or ‘Threatened’. Understanding the risks posed to lizards will help to inform successful management of vulnerable populations.  I used lizard-mimicking replicas to identify and assess predation rates exerted by bird species on lizard populations within the Wellington region of New Zealand. I examined the use of lizard replicas as a tool to quantify predation by examining how birds interacted with replicas and comparing attack rates with novel items simultaneously placed in the field. I determined which bird species were preying on replicas, the extent of such predation, and whether site vegetation or daily weather influenced the probability of avian attack on replicas. Although attack frequency did not differ between novel items and lizard replicas, birds exhibited a realistic predatory response by preferentially attacking the head of lizard replicas. Interactions by birds with lizard-mimicking replicas cannot be confirmed as true predation attempts, but lizard replicas can nevertheless be used to quantify predation pressures exerted on lizard populations by opportunistic bird species.   Seven ground-foraging bird species were found to attack lizard replicas. Two species, the pūkeko (Porphyrio melanotus melanotus) and southern black-backed gull (Larus dominicanus dominicanus), were identified as high impact species. The average predation risk experienced by lizard replicas varied greatly across environments, with 0 – 25% of replicas attacked daily at sites. Canopy cover and daily rainfall were not significant predictors, but potentially decreased the likelihood of replica attack. Predation risk varied for lizard replicas as a result of differing assemblages of bird predators at sites, and the presence and foraging behaviour of specific predatory birds.   Predation by birds is likely to be an issue where predation pressure is high, or lizard populations are small, range restricted, or recovering from the presence of mammalian predators. When managing vulnerable lizard populations, managers should take into account the threats posed by avian predators so that lizard communities can recover successfully following the same trajectory as native birds.</p>


2021 ◽  
Author(s):  
◽  
Brittany Florence-Bennett

<p>Wildlife management is fraught with challenges due to the complexities of community ecology. Interventions aimed at restoring ecosystems, or managing species, can have unintended negative outcomes for target species. The effect of avian predation on native lizard fauna in New Zealand is not clearly understood, despite birds being regarded as top predators within mammal-free ecosystems. At least thirty-one species of bird have been recorded preying on native lizards, but few studies have directly addressed avian predation on lizards, with the majority of evidence sourced from published anecdotes. New Zealand’s herpetofauna are already vulnerable due to range contractions resulting from mammalian predation and habitat loss, with 87% of New Zealand lizard species considered ‘At Risk’ or ‘Threatened’. Understanding the risks posed to lizards will help to inform successful management of vulnerable populations.  I used lizard-mimicking replicas to identify and assess predation rates exerted by bird species on lizard populations within the Wellington region of New Zealand. I examined the use of lizard replicas as a tool to quantify predation by examining how birds interacted with replicas and comparing attack rates with novel items simultaneously placed in the field. I determined which bird species were preying on replicas, the extent of such predation, and whether site vegetation or daily weather influenced the probability of avian attack on replicas. Although attack frequency did not differ between novel items and lizard replicas, birds exhibited a realistic predatory response by preferentially attacking the head of lizard replicas. Interactions by birds with lizard-mimicking replicas cannot be confirmed as true predation attempts, but lizard replicas can nevertheless be used to quantify predation pressures exerted on lizard populations by opportunistic bird species.   Seven ground-foraging bird species were found to attack lizard replicas. Two species, the pūkeko (Porphyrio melanotus melanotus) and southern black-backed gull (Larus dominicanus dominicanus), were identified as high impact species. The average predation risk experienced by lizard replicas varied greatly across environments, with 0 – 25% of replicas attacked daily at sites. Canopy cover and daily rainfall were not significant predictors, but potentially decreased the likelihood of replica attack. Predation risk varied for lizard replicas as a result of differing assemblages of bird predators at sites, and the presence and foraging behaviour of specific predatory birds.   Predation by birds is likely to be an issue where predation pressure is high, or lizard populations are small, range restricted, or recovering from the presence of mammalian predators. When managing vulnerable lizard populations, managers should take into account the threats posed by avian predators so that lizard communities can recover successfully following the same trajectory as native birds.</p>


Insects ◽  
2021 ◽  
Vol 12 (8) ◽  
pp. 720
Author(s):  
Jacques Régnière ◽  
Lisa Venier ◽  
Dan Welsh

The impact of avian predation on a declining population of the spruce budworm, Choristoneura fumifereana (Clem.), was measured using single-tree exclosure cages in a mature stand of balsam fir, Abies balsamea (L.), and white spruce, Picea glauca (Moench.) Voss. Bird population censuses and observations of foraging and nest-feeding activity were also made to determine the response of budworm-linked warblers to decreasing food availability. Seasonal patterns of foraging. as well as foraging success in the declining prey population was compared to similar information from birds observed in another stand where the spruce budworm population was rising. Avian predation was an important source of mortality between the 4th instar and moth emergence in the declining outbreak population. Mortality by predation increased from negligible to over 98% as budworm density dropped from 100 to <1 larva/kg of host foliage, over 3 years. Calculations based on nest-feeding activity and basic metabolic demands support these observed rates. Seasonal and yearly differences in predation rates observed between the two host-tree species correspond to equivalent shifts in bird foraging behavior in response to dropping insect density. In particular, a preference for searching on white spruce disappeared, although budworm-linked birds remained more efficient at finding food on this plant. The ability to change foraging behavior as prey density dropped differed between bird species.


PLoS ONE ◽  
2021 ◽  
Vol 16 (1) ◽  
pp. e0244733
Author(s):  
Wim C. Mullié ◽  
Robert A. Cheke ◽  
Stephen Young ◽  
Abdou Baoua Ibrahim ◽  
Albertinka J. Murk

The entomopathogenic fungus Metarhizium acridum in oil-based formulations (Green Muscle® (GM)) is a biopesticide for locust control lacking side-effects on biodiversity, unlike chemical insecticides. Under controlled conditions, GM-treated locusts and grasshoppers attract predators, a complementary advantage in locust control. We assessed avian predation on a population of desert locusts in northern Niger aerially sprayed operationally with GM with 107 g viable conidia ha-1. Populations of adult locusts and birds and vegetation greenness were assessed simultaneously along two transects from 12 days before until 23 days after treatment. Common kestrels Falco tinnunculus and lanners F. biarmicus were the predominant avian predators. Regurgitated pellets and prey remains were collected daily beneath “plucking posts” of kestrels. Locusts started dying five days post-spray and GM had its maximum effect one-two weeks after the spray, with 80% efficacy at day 21. After spraying, bird numbers increased significantly (P<0.05) concurrent with decreasing desert locust densities. Locust numbers decreased significantly (P<0.001) with both time since spraying and decreasing greenness. Before spraying, kestrel food remains under plucking posts accounted for 34.3 ±13.4 prey items day-1, of which 31.0 ±11.9 were adult desert locusts (90.3%), reducing post-spray to 21.1 ±7.3 prey items day-1, of which19.5 ±6.7 were adult desert locusts (92.5%), attributable to decreased use of the plucking-posts by the kestrels rather than an effect of the spray. After spraying, kestrels took significantly (P<0.05) more larger female (75–80%) than smaller male (20–25%) locusts. Avian predation probably enhanced the impact of the GM on the desert locust population, especially by removing large adult females. No direct or indirect adverse side-effects were observed on non-target organisms including locust predators such as ants and birds. These substantial ecological advantages should also be considered when choosing between conventional chemical and biopesticide-based locust control.


Author(s):  
Ganesh Kumar ◽  
Shraddha Hegde ◽  
David Wise ◽  
Charles Mischke ◽  
Brian Dorr

2020 ◽  
Vol 84 (6) ◽  
pp. 1164-1178
Author(s):  
Steven L. Haeseker ◽  
Gabriel Scheer ◽  
Jerry McCann

2019 ◽  
Vol 148 (5) ◽  
pp. 896-913
Author(s):  
Allen F. Evans ◽  
Quinn Payton ◽  
Bradley M. Cramer ◽  
Ken Collis ◽  
Nathan J. Hostetter ◽  
...  

2019 ◽  
Vol 9 (3) ◽  
pp. 1083-1094 ◽  
Author(s):  
Karen M. Thorne ◽  
Kyle A. Spragens ◽  
Kevin J. Buffington ◽  
Jordan A. Rosencranz ◽  
John Takekawa
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