scholarly journals A Nest Predator's View of a Managed Forest: Gray Jay (Perisoreus Canadensis) Movement Patterns in Response to Forest Edges

The Auk ◽  
2004 ◽  
Vol 121 (1) ◽  
pp. 162-169 ◽  
Author(s):  
Jacques Ibarzabal ◽  
André Desrochers

Abstract High nest-predation risk is often associated with forest edges. Most nest predators in boreal coniferous forests of North America are forest specialists living in mature stands. Nest predators have been studied mainly through use of artificial nests; knowledge of their behavior remains limited. We used radiotelemetry to examine movement patterns, relative to forest edge, of a forest nest predator, the Gray Jay (Perisoreus canadensis), in boreal coniferous forest. Each of 11 family groups of Gray Jays monitored in early summer exhibited a marked association with forest edges. Jays were found within 30 m of the forest edges more often than expected from random use of mature forest. Furthermore, jays traveled more slowly near forest edges than in the forest interior. Because forest edges apparently represent prime foraging habitat for Gray Jays, narrow forest strips left by logging could act as ecological traps for mature-stand songbirds before stands regenerate in adjacent clearcuts.

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.


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.


The Condor ◽  
2000 ◽  
Vol 102 (2) ◽  
pp. 256-266 ◽  
Author(s):  
Maiken Winter ◽  
Douglas H. Johnson ◽  
John Faaborg

Abstract We tested how edges affect nest survival and predator distribution in a native tallgrass prairie system in southwestern Missouri using artificial nests, natural nests of Dickcissels (Spiza americana) and Henslow's Sparrows (Ammodramus henslowii), and mammal track stations. Survival of artificial nests was lower within 30 m of forest edge. Nesting success of Dickcissels and Henslow's Sparrows was lower within 50 m to a shrubby edge than at greater distances, whereas fates of nests were not related to distances to roads, agricultural fields, or forests. Evidence from clay eggs placed in artificial nests indicated that mid-sized carnivores were the major predators within 30 m of forest edges. Furthermore, mid-sized carnivores visited track stations most frequently within 50 m of forest edges. Because proximity of woody habitat explained more variation in nest survival and mammal activity than did fragment size, it appears that edge effects were more pronounced than area effects. Edge effects appeared to be caused mainly by greater exposure of nests to mid-sized carnivores. We argue that, based on edge avoidance behavior, “grassland-interior” species such as the Henslow's Sparrow respond to edge effects mainly by a decrease in density, whereas habitat generalists such as the Dickcissel are affected mainly by a decrease in nesting success.


Author(s):  
Noah Atkin ◽  
Cris Banks-Leite

It has been previously hypothesised that nest predation is higher at forest edges. This has important conservation implications for the increasingly fragmented U.K. climax community. I aimed to test the generality of this edge effect in a mixed deciduous forest fragment which borders open grassland. Artificial nests containing a combination of quail and plasticine eggs were used, at ground and arboreal levels. I found an overall edge effect on nest predation rates, however this effect was not specifically seen in ground nests. Ground nests experienced significantly higher levels of predation than arboreal nests. I suggest this edge effect is due in part to the steep productivity gradient over the ecotone.


2003 ◽  
Vol 30 (2) ◽  
pp. 119 ◽  
Author(s):  
Rebecca L. Boulton ◽  
Michael F. Clarke

We tested the hypothesis that predation rates increase near habitat edges and can cause low reproductive success in forest bird species living in a fragmented habitat. We constructed artificial yellow-faced honeyeater (Lichenostomus chrysops) nests and placed them 5 m, 20 m, 50 m and 200 m from the forest edge. We also monitored natural yellow-faced honeyeater nests at varying distances from the forest edge. Artificial nests experienced 43% predation over the 14-day exposure period, while natural yellow-faced honeyeater nests experienced 28% during the incubation period and 47% during the nestling period. No negative edge effect was detected for artificial or natural nests. In fact, natural nests experienced higher nest success closer to the forest edge. There was no increase in the number of avian predators recorded at the forest edge, even though birds were identified as the main predators at artificial nests (49%). The lack of support for both the 'ecological trap' and 'predator influx' hypotheses contributes to a growing body of evidence that suggests that not all species surviving in highly fragmented environments are negatively affected by edge effects.


1972 ◽  
Vol 2 (2) ◽  
pp. 127-151 ◽  
Author(s):  
Yoshika Oniki ◽  
Edwin O. Willis

Abstract Birds that prey on arthropods flushed by army ants north of the eastern Amazon were studied at Serra do Navio and Reserva Ducke (Brazil) and at Nappi Creek and Bartica (Guyana). Regular ant-followers are two medium-sized antbirds (Percnostola rufifrons and Gymnopithys rufigula) and two smaller ones (Pithys albifrons and Hylophylax poecilonota), plus five woodcreepers of differing sizes (from very large Hylexetastes perrotti through Dendrocolaptes picumnus, D. certhia, and Dendrocincla merula to medium-sized Dendrocincla fuliginosa). Four other regular ant-followers occur in the region but were not found at the study areas. Forty-five species of casual or nonprofessional ant-followers, including 16 antbirds, 5 woodcreepers, and 5 manakins, also were recorded. Percnostola rufifrons tends to be at the forest edge or in second growth. Pithys albifrons works around Gymnopithys rufigula, Hylophylax poecilonota peripheral to both, in the forest interior. The large Dendrocolaptes picumnus and medium-large Dendrocincla merula often capture prey near the ground, like antbirds. Unlike antbirds, which use vertical or horizontal slender perches, the woodcreepers use thick vertical perches. Dendrocolaptes certhia and Dendrocincla fuliginosa also tend to capture prey high over the ground-foraging antbirds. The woodcreepers tend to forage lower at midday. Hylexetastes perrotti is rare, and overlaps strongly with D. picumnus. There is fairly large overlap among the 9 professional ant-followers, and large ones chase away smaller ones. Nonprofessional birds tend to forage briefly or peripherally when or slightly after the professional species are active. They also forage above the antbirds and below or above the woodcreepers, and concentrate at forest edges or in second growth. The guild of ant-following birds in this region differs fairly widely from guilds in Panamá and at Belém, Brazil; the absence of large antbirds and the predominance of large woodcreepers north of the Amazon are the major differences.


2008 ◽  
Vol 38 (10) ◽  
pp. 2616-2625 ◽  
Author(s):  
Raul Rosenvald ◽  
Asko Lõhmus ◽  
Andres Kiviste

Survival of live retention trees is a key issue for stand-scale applications of natural-disturbance-based silviculture. We explored the survival of 3255 trees in 102 cut areas (mean size 2.3 ha) in Estonia for 6 years, focusing on spatial variation and preadaptation of the trees. Altogether, 35% of the trees died during the study period, contributing 4.4 m3 of downed dead trunks and 1 m3 of standing dead trees per hectare. The annual mortality rates declined over time. The main survival determinants were tree species (higher for hardwood deciduous trees), diameter (species dependent), position relative to forest edge (higher for trees near current or former forest edges), retention density (positive), and exposure (negative). The results suggest that (1) green-tree retention can effectively increase the abundance of large shade-tolerant trees, but it is equally important for producing deadwood; (2) larger individuals, former interior-forest trees near current forest edges, and preadapted trees in open conditions should be preferably retained; (3) there is no obvious necessity to modify tree-retention techniques for tree survival according to geographical region or forest site type.


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