Pine forest structure in a human-dominated landscape system in Korea

To elucidate the characteristics of spatial heterogeneity in a human-dominated landscape, vegetation and community structure of pine (Pinus densiflora andP. rigida) forests were studied at rural Teokseong-ri in Chollanam-do, in the southwestern part of Korea. Daily removal of undergrowth for firewood affects the stratification and species composition in the community. In general, stratification of the pine forest develops in proportion to its distance from the main habitat of farmers, involving the residential and cultivated land. In pine forests near the main habitat of farmers, sun-demanding herbaceous plants grow well, while in remote forests, Fagaceous plants such asQuercus serrata, Q. actissima andCastanea crenata grow well. This zonation results from the fact that removal of undergrowth is greater in the forest near the main habitat of farmers, than in the remote forest. Construction and maintenance of graveyards, however, prevents development of stratification of the forest even in remote stands.     

Cropland edge,forest succession,and landscape affect shrubland bird nest predation

The effects of habitat edges on nest survival of shrubland birds, many of which have experienced significant declines in the eastern United States, have not been thoroughly studied. In 2007 and 2008, we collected data on nests of 5 shrubland passerine species in 12 early successional forest patches in North Carolina, USA. We used model selection methods to assess the effect of distance to cropland and mature forest edge on nest predation rates and additionally accounted for temporal trends, nest stage, vegetation structure, and landscape context. For nests of all species combined, nest predation decreased with increasing distance to cropland edge, by nearly 50% at 250 m from the cropland edge. Nest predation of all species combined also was higher in patches with taller saplings and less understory vegetation, especially in the second year of our study when trees were 4–6 m tall. Predation of field sparrow (Spizella pusilla) nests was lower in landscapes with higher agricultural landcover. Nest predation risk for shrubland birds appears to be greater near agricultural edges than mature forest edges, and natural forest succession may drive patterns of local extirpation of shrubland birds in early successional forest patches. Thus, we suggest that habitat patches managed for shrubland bird populations should be considerably large or wide (>250 m) when adjacent to crop fields and maintained in structurally diverse early seral stages. © 2011 The Wildlife Society.     

Forest fragmentation and rhinocryptid nest predation in central Chile

Fragmentation of forest landscapes can raise the intensity of nest predation by increasing the abundance and richness of generalist or introduced predators. Understory foraging birds, such as rhinocryptids, can be highly vulnerable to nest predation in fragmented landscapes because they often place their nests on the ground. Temperate deciduous forests in Chile have been intensively fragmented in the last centuries, causing changes in nest predator densities. We tested if predation of artificial nests, mimicking those of rhinocryptids, placed on and above ground was higher in the remnant fragments of central Chile due to an increase in predator abundance. The rate of nest predation in forest remnants was larger than in native continuous forest. Small mammals were the main nest predators. Despite high predation rates, the abundance of rhinocryptids is higher in forest remnants, suggesting that fragments might constitute ecological traps.     

Factors affecting nest predation on forest songbirds in North America

Nest predation is an important factor in the ecology of passerines and can be a large source of mortality for birds. I provide an overview of factors affecting nest predation of passerines in North America with the goal that it may provide some insight into the ecology and management of woodland birds in the United Kingdom. Although several factors influence productivity, nest success is perhaps the most widely measured demographic characteristic of open-cup-nesting birds, and nest predation is usually the largest cause of nest failure. The identity of predator species, and how their importance varies with habitat and landscape factors, must be known for managers and scientists to design effective conservation plans and place research on nest predation in the appropriate context. Recent studies using video surveillance have made significant contributions to our understanding of the relative importance of different predator taxa in North America. Spatial and temporal variation in nest predation can be better understood when landscapes are placed in a biogeographical context and local habitat and nest-site effects are placed in a landscape context. Low productivity resulting from high nest predation is one of several potential causes of bird population declines in North America and the UK. Although the 'forest fragmentation paradigm' from the eastern US may not apply directly to the UK, thinking about avian demographics from a multiscale perspective, and consideration of factors affecting nest predation with knowledge of the dominant predator species, may provide insight into population declines.     

Forest fragmentation relaxes natural nest predation in an Afromontane forest

Nest predation is widely regarded as a major driver underlying the population dynamics of small forest birds. Following forest fragmentation and the subsequent invasion by species from non-forested landscape matrices, shifts in predator communities may increase nest predation near forest edges. However, effects of human-driven habitat change on nest predation have mainly been inferred from studies with artificial nests, despite being regarded as poor surrogates for natural ones. We studied variation in predation rates, and relationships with timing of breeding and characteristics of microhabitats and fragments, on natural white-starred robin Pogonocichla stellata nests during three consecutive breeding seasons (2004–2007) in a Kenyan fragmented cloud forest. More than 70% of all initiated nests were predated during each breeding season. Predation rates nearly quadrupled between the earliest and the latest nests within a single breeding season, increased with distance to the forest edge, and decreased with the edge-to-area ratio of forest fragments. These spatial relationships oppose the traditional perception of edge and fragmentation effects on nest predation, but are in line with results from artificial nest experiments in other East African forests. In case of inverse edge and fragmentation effects on nest predation, such as shown in this study, species that tolerate edges for breeding may be affected positively, rather than negatively, by forest fragmentation, while the opposite can be expected for species restricted to the forest interior. The possibility of inverse edge effects, and its conservation implications, should therefore be taken into account when drafting habitat restoration plans.     

Artificial nest predation rates in tropical and temperate forests: a review of the effects of edge and nest site

Nest predation rates are believed to be higher in tropical than in temperate forests. This notion is central in explaining different life history traits of tropical and temperate birds, but it is not known whether this assertion is true for all nest sites, such as ground and shrub nests, and at different distances from forest edge. I reviewed 22 studies using artificial nest experiments which concurrently contrasted predation rates of ground and shrub nests in temperate and tropical forests and found, contrary to the current dogma, no overall difference in predation rates between regions. However, there was a significant interaction between region and nest site. Ground nest predation rates were significantly higher in the tropical region, while predation rates on shrub nests were similar between regions. Within the tropical region, ground nests had significantly higher predation rates than shrub nests. Elevated nest predation rates at forest edges were found in both temperate and tropical forests. The results may have great implications for expected patterns of avian life histories and for the effects of forest fragmentation in temperate and tropical regions. First, if nest predation affects avian life histories, my results predict ground-nesting species in tropical forests to have shorter nestling periods, more broods and smaller clutch sizes than shrub-nesting species. Second, vulnerability of ground- and shrub-nesting guilds is suggested to differ between regions due to differences in forest vegetation structure, and the composition of predator faunas and their specific responses to forest fragmentation. Data to test these hypotheses are limited, but agree with the results of this review.     

Artificial nest and seed predation experiments on tropical southeast Asian islands

Southeast Asia is rapidly losing native habitats and the consequences of this are poorly understood. Because habitat loss and disturbance can affect avian and seed survivorship, we conducted artificial nest and seed predation experiments on tropical southeast Asian islands. Data among islands and fragments or different forest types (e.g. primary versus exotic forest) within the islands are compared. On Singapore Island, predation among different forest types (primary, secondary and woodland) did not differ. Only at one of the sites, nest predation was higher at 75 m from the forest edge than at 25 m. In other sites, predation did not differ in relation to the distance from the forest edge. Predation among 10 small (0.8–1026 ha) Singaporean islands differed. However, none of the environmental variables (e.g. island area) could explain the predation differences. The lowest predation of both nests and seeds was recorded in the primary forest areas of a contiguous forest (25 500 ha) in central Java (Linggoasri). Small mammals were the main predators on Singapore and other surrounding islands. However, the index of potential predator abundance, overall, did not correlate with predation. While larger and more pristine forests may be better for avian and seed survivorship, pinpointing variables affecting both artificial nest and seed predation may be difficult.     

Effects of nest features and surrounding landscape on predation rates of artificial nests

Artificial nest predation experiments were carried out in northern Italy in woods which varied in size, isolation and surrounding landscape structure. Multivariate analyses, including logistic regression, showed that: (1) size and isolation of woods did not significantly affect predation rates; (2) nests on the edge of woods did not suffer higher predation rates than nests inside the wood; (3) nest camouflage greatly influenced predation rates, suggesting that predators were mainly using visual clues to identify nests; (4) the type of habitat that surrounded the woods emerged as a crucial factor in nest survival and the amount of human settlements in the vicinity of the wood was inversely correlated with nest survival, probably due to predators associated with humans; (5) other habitat variables, which were apparently individually unimportant, were found to have an effect on nesting success, if combined in a single ‘suitability index’. It is impossible to generalize about the influence of landscape fragmentation on nest predation because local landscape history and predator guilds, together with the scale of fragmentation, probably interact to determine the suitability of nest sites and their vulnerability to predators.     

Artificial nest predation rates vary among habitats in the Australian monsoon tropics

Rates of nest predation have frequently been shown to differ between fragmented and unfragmented habitats, but have rarely been compared among natural habitats in the same geographic region. In this study, artificial nests of two types (open cup and domed) were placed in four habitats (mangroves, monsoon rainforests, eucalypt woodlands and paperbark swamps) over 12 months in three localities near Darwin in the Australian monsoon tropics to determine the effects of habitat, season and nest type on the rate of nest predation. A quail egg and a similarly coloured plasticine egg were placed in each nest. Habitat had a strong effect on nest predation rates, with nests in mangroves experiencing predation rates more than four times higher than those in eucalypt woodlands and paperbark swamps. Despite the strong rainfall seasonality of the region, there was no consistent seasonal variation in nest predation rates. Nest type also had little influence on predation rates, except in paperbark swamps where open cup nests suffered a higher predation rate than domed nests. The study indicates that generalised nest predation rates for tropical regions, even for small areas (e.g. <17 km radius), might overlook substantial variation between habitats. Such variation confounds purported differences in nest predation rates between tropical and temperate regions.     

Artificial nest predation and habitat fragmentation: different trends in bird and mammal predators

Predation on artificial nests was studied in Belgian deciduous forest fragments between 1 and 200 ha Predation rates were compared to fragment size, distance from the forest edge, time period (three replicates), and nest type (ground and tree) Logistic regression analysis showed that overall nest predation did not vary with distance from the edge, forest size, and time period Birds represented over 70% of all predator attacks but their importance decreased in larger areas and away from the forest edge where mammals were responsible for much of the nest predation It is concluded that the effect of habitat fragmentation depends on the composition of the local predator community     

Different nest predator faunas and nest predation risk on ground and shrub nests at forest ecotones: an experiment and a review

This study examined predator faunas of artificial ground and shrub nests and whether nest predation risk was influenced by nest site, proximity to forest edge, and habitat structure in 38 grassland plots in south-central Sweden. There was a clear separation of predator faunas between shrub and ground nests as identified from marks in plasticine eggs. Corvids accounted for almost all predation on shrub nests whereas mammals mainly depredated ground nests. Nest predation risk was significantly greater for shrub than for ground nests at all distances (i.e. 0, 15 and 30 m) from the forest edge. However, nest predation risk was not significantly related to distance to forest edge, but significantly increased with decreasing distance to the nearest tree. Different corvid species robbed nests at different distances from the forest edge, with jays robbing nests closest to edges. We conclude that the relationship between the predation risk of grassland bird nests and distance to the forest edge mainly depends on the relative importance of different nest predator species and on the structure of the forest edge zone. A review of published articles on artificial shrub and ground nest predation in the temperate zone corroborated the results of our own study, namely that shrub nests experienced higher rates of depredation in open habitats close to the forest edge and that avian predators predominantly robbed shrub nests. Furthermore, the review results showed that predation rates on nests in general are highest <50 m inside the forest and lower in open as well as forest interior habitats (≥50 m from the edge). Received: 16 March 1998 / Accepted: 30 July 1998     

Dung beetle assemblages in primary forest and disturbed habitats in a tropical dry forest landscape in western Mexico

Dung beetles (Scarabaeinae) are conspicuous components in most terrestrial ecosystems, performing important ecological functions and services. Being sensitive to several types of disturbance, they have been successfully used as indicators of habitat change. Dung beetle communities in tropical rainforests have been well studied, but considerably less information is available for tropical dry forests. In this study I sampled dung beetles in two undisturbed habitats, deciduous forest and semideciduous forest, and two disturbed habitats, secondary forest and open area habitat, in the Chamela-Cuixmala region of western Mexico. Dung beetle species with high indicator value for each habitat were identified. Beetle abundance, observed species richness and estimated species richness were similar in the three forest habitats, but significantly lower in the open area habitat. A more detailed analysis of species-specific abundances in the three forest habitats revealed some differences. Transects of one of the undisturbed habitats, the deciduous forest, were more similar to the non-adjacent transects of disturbed secondary forest, than to the adjacent undisturbed semideciduous forest transects. Unlike studies in other tropical sites that have found a decrease in equitability in Scarabaeinae assemblages between undisturbed forest and disturbed habitat (particularly open habitats), in the Chamela-Cuixmala region all four habitats showed similar low equitability in community structure, with two or three very dominant species.     

Associations between primates and other mammals in a central Amazonian forest landscape

Little information exists on mixed-species groups between primates and other mammals in Neotropical forests. In this paper, we describe three such associations observed during an extensive large-vertebrate survey in central Amazonia, Brazil. Mixed-species groups between a primate species and another mammal were observed on seven occasions between squirrel monkeys (Saimiri cf. ustus) and either South American coatis (Nasua nasua) or tayras (Eira barbara) and between brown capuchins (Cebus apella) and coatis. All associations were restricted to floodplain forest during its dry stage. We suggest that the associations involving the coatis are connected to foraging and vigilance but may be induced by a common alternative food resource at a time of food shortage.     

The influence of landscape features on nest predation rates of grassland‐breeding waders

In Europe, lowland wet grasslands have become increasingly fragmented, and populations of waders in these fragments are subject to unsustainably high levels of nest predation. Patches of taller vegetation in these landscapes can support small mammals, which are the main source of prey for many predators. Providing such patches of habitat could potentially reduce levels of nest predation if predators preferentially target small mammals. However, predator attraction to patches of taller vegetation for foraging, shelter, perching and/or nesting could also result in local increases in predation rates, as a consequence of increased predator densities or spill‐over foraging into the surrounding area. Here we assess the influence of taller vegetation on wader nest predation rates, and the feasibility of managing vegetation structure to alter predator impacts. Between 2005 and 2011, the nest distribution and hatching success of Northern Lapwings Vanellus vanellus, which nest in the open, and Common Redshanks Tringa totanus, which conceal their nests in vegetation, were measured on a 487‐ha area of wet grassland in eastern England that is primarily managed for breeding waders. Predation rates of Lapwing nests increased significantly with distance from patches of taller vegetation, and decreased with increasing area of taller vegetation within 1 km of the nest, whereas neither variable influenced Redshank nest predation probability. These findings suggest that the distribution and activity of nest predators in lowland wet grassland landscapes may be influenced by the presence and distribution of areas of taller vegetation. For Lapwings at least, there may therefore be scope for landscape‐scale management of vegetation structure to influence levels of predation in these habitats.     

Temporal variation in nest predation risk along habitat edges between grassland and secondary forest in Central Europe

Habitat fragmentation alters many ecological processes, including trophic cascades. For example, increased predation pressure along habitat edges has often been observed in fragmented landscapes. Here, we studied how nest predation risk varies along the transition zone between grassland and mixed forest in Central Europe. Using artificial nests, we tested the two mechanisms that are expected to underlie higher predation rates along edges: (1) the matrix effect model that supposes predator penetration from a habitat type with higher predator density to one with lower predator density and (2) the ecotonal effect model that assumes specific predator preferences for habitat edges. Although our results do not fully support either of these scenarios, our data show high temporal instability in nest predation along forest–grassland edges. Predation was higher in habitat interiors compared to edges during the first year, whereas the opposite pattern was observed during the subsequent year. In addition, dramatic between-year differences in the species composition of nest predators were observed. Therefore, we hypothesise that the effect of edges on nest predation is difficult to predict in landscapes with high predator diversity. In addition, our data indicate that a high abundance of wild boar considerably increases the risk of predation for ground-nesting birds.     

Density-dependent nest predation in waterfowl: the relative importance of nest density versus nest dispersion

When nest predation levels are very high or very low, the absolute range of observable nest success is constrained (a floor/ceiling effect), and it may be more difficult to detect density-dependent nest predation. Density-dependent nest predation may be more detectable in years with moderate predation rates, simply because there can be a greater absolute difference in nest success between sites. To test this, we replicated a predation experiment 10 years after the original study, using both natural and artificial nests, comparing a year when overall rates of nest predation were high (2000) to a year with moderate nest predation (2010). We found no evidence for density-dependent predation on artificial nests in either year, indicating that nest predation is not density-dependent at the spatial scale of our experimental replicates (1-ha patches). Using nearest-neighbor distances as a measure of nest dispersion, we also found little evidence for "dispersion-dependent" predation on artificial nests. However, when we tested for dispersion-dependent predation using natural nests, we found that nest survival increased with shorter nearest-neighbor distances, and that neighboring nests were more likely to share the same nest fate than non-adjacent nests. Thus, at small spatial scales, density-dependence appears to operate in the opposite direction as predicted: closer nearest neighbors are more likely to be successful. We suggest that local nest dispersion, rather than larger-scale measures of nest density per se, may play a more important role in density-dependent nest predation.     

Linking songbird nest predation to seedling density: Sugar maple masting as a resource pulse in a forest food web

The ecological literature presents considerable evidence for top‐down forcing on the maintenance of species diversity. Yet, in temperate forests, bottom‐up forces often exert a strong influence on ecosystem functioning. Here, we report on the indirect influence of a pulsed resource, sugar maple (Acer saccharum) seed production, on nest survival in a migratory songbird. We hypothesized that seed production in year t would determine daily nest survival rate in year t + 1 through its effects on seed‐eating rodents. We used the density of sugar maple seedlings (with cotyledons) in year t + 1 as a proxy for seed production in year t and predicted that it would be inversely related to songbird nest survival the same year. We estimated the density of sugar maple seedlings, eastern chipmunk (Tamias striatus) activity, and daily nest survival rate in the ovenbird (Seiurus aurocapilla) over four successive years in a northern hardwood forest of New Brunswick, Canada. Seedling density varied by two orders of magnitude between years, whereas an index of chipmunk activity changed by an order of magnitude. Both variables were positively correlated and negatively correlated to daily nest survival rate. A logistic‐exposure model including only seedling density received the greatest level of support (lowest AIC_c). Previous studies have reported the effect of sugar maple masting on seed‐eating rodent populations, but the strong link we report between seedling density and songbird nest survival is novel. A nocturnal seed‐eating nest predator, deer mouse (Peromyscus maniculatus), was not considered in our models, which may explain why chipmunk was not the best predictor of daily nest survival rate. The trophic linkages we observed are remarkably strong for a temperate forest ecosystem and might become more prevalent in northeastern North America, at least on calcium‐rich soils, with the loss of large‐diameter beech trees as a result of beech bark disease.