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.     

Current nest box designs may not be optimal for the larger forest dormice: Pre‐hibernation increase in body mass might lead to sampling bias in ecological data

1. Biologists commonly use nest boxes to study small arboreal mammals, including the forest dormouse (Dryomys nitedula). Hibernating dormouse species often experience pronounced seasonal variations in body mass, which might lead to sampling biases if it is not taken into account when designing nest boxes. In my study of the forest dormouse, I noticed that the entrance hole of nest boxes had been gnawed. I hypothesized that this behavior was exhibited by the individual dormice of higher body mass, who were unable to pass through the entrance holes.
2. To test my hypothesis, I categorized the individual dormice present inside nest boxes based on their body mass and then compared the seasonal body mass dynamics with the timing of the gnawing behavior. I also compared nest box occupancy by the forest dormouse before and after the gnawing behavior.
3. Interestingly, I found that the gnawing behavior was displayed exclusively when part of the dormouse population increased considerably in body mass, which supports my hypothesis. Additionally, nest box occupancy decreased significantly from 20% before to 4.6% after the gnawing behavior.
4. I suggest that researchers include nest boxes with entrance holes larger than 4 cm in future studies of the forest dormouse to prevent the possible exclusion of the conspecifics that have higher body mass before hibernation. This type of sampling bias might also concern studies of other species, such as the fat dormouse, that similarly show pronounced seasonal variations in body mass. I recommend that biologists consider the seasonal body mass dynamics of the target species when designing nest boxes to minimize bias in ecological data and improve management actions.

     

Nest‐site selection by Slender‐billed Parakeets in a Chilean agricultural‐forest mosaic

ABSTRACT Species in the family Psittacidae may be particularly vulnerable to anthropogenic habitat transformations that reduce availability of suitable breeding sites at different spatial scales. In southern Chile, loss of native forest cover due to agricultural conversion may impact populations of Slender‐billed Parakeets (Enicognathus leptorhynchus), endemic secondary cavity‐nesting psittacids. Our objective was to assess nest‐site selection by Slender‐billed Parakeets in an agricultural‐forest mosaic of southern Chile at two spatial scales: nest trees and the habitat surrounding those trees. During the 2008–2009 breeding seasons, we identified nest sites (N= 31) by observing parakeet behavior and using information provided by local residents. Most (29/31) nests were in mature Nothofagus obliqua trees. By comparing trees used for nesting with randomly selected, unused trees, we found that the probability of a tree being selected as a nest site was positively related to the number of cavity entrances, less dead crown, and more basal injuries (e.g., fire scars). At the nesting‐habitat scale, nest site selection was positively associated with the extent of basal injuries and number of cavity entrances in trees within 50 m of nest trees. These variables are likely important because they allow nesting parakeets to minimize cavity search times in potential nesting areas, thereby reducing energetic demands and potential exposure to predators. Slender‐billed Parakeets may thus use a hierarchical process to select nest sites; after a habitat patch is chosen, parakeets may then inspect individual trees in search of a suitable nest site. Effective strategies to ensure persistence of Slender‐billed Parakeets in agricultural‐forest mosaics should include preservation of both individual and groups of scattered mature trees.     

Nesting habitat characteristics of Marbled Murrelets occurring in near‐shore waters of the Olympic Peninsula,Washington

Marbled Murrelets (Brachyramphus marmoratus) are listed as threatened in the portion of their range extending from British Columbia to California due to loss of nesting habitat. Recovery of Marbled Murrelet populations requires a better understanding of the characteristics of their nesting habitat in this part of their range. Our objective, therefore, was to describe their nesting habitat in Washington State and Vancouver Island, British Columbia. We captured Marbled Murrelets from 2004 to 2008, fitted them with radio transmitters, and followed them to nests (N = 20). We used Cohen's unbiased d effect size to assess differences between forest plots surrounding nest sites and nearby control sites (N = 18). Nest sites had less canopy cover of the dominant conifers and fewer, but larger, trees than control sites. Nest sites also had greater percentages of trees with platforms >10 cm diameter and >15 cm diameter, and more platforms of these sizes than control sites. The mean diameter at breast height of nest trees was 136.5 cm (range = 84–248 cm) and all but one nest was in dominant or co‐dominant tree species. At the landscape scale, we used vegetation maps derived from remotely sensed data and found greater canopy cover, higher density of mature trees, more platforms >10 cm/ha, and more old‐growth habitat at nest sites than at random sites. Our findings suggest that, at the site scale, nesting Marbled Murrelets selected the most suitable features of forest structure across expansive potentially suitable habitat. Our landscape‐scale analysis showed that habitat features in nesting stands differed from those features in available stands in the murrelet's range in Washington. We also found that stands with nests were less fragmented than available forest across murrelet range. All nest sites of radio‐tagged birds in Washington were in protected areas in mostly undisturbed forest habitat. Conservation of these areas of inland nesting habitat will be critical to the recovery of Marbled Murrelet populations.     

Predation on artificial nests in a forest dominated landscape – the effects of nest type, patch size and edge structure

We studied the effects of forest patch size and forest edge structure on nest predation in a boreal coniferous forest landscape. The following predictions were tested. Nest predation should be higher in small than in large stands, in edges than in interior areas of forest stands, and in barren forest/clear–cut edges created by forestry than in natural forest/open marsh edges. Four types of artificial above ground nests (total of 261) were used; open cup nests with reindeer Rangifer t. tarandus hair, open cup nests with domestic hen Gallus domesticus feathers, and unlined open cup and nest–box nests. Nests were baited with one Japanese quail Coturnix coturnix japonica egg. Nest–boxes were depredated significantly less than open cup nests of all types. No edge- or stand size–related nest predation was found. The predation rate, regardless of the nest type, did not differ relative to the edge type and vegetation characteristics. However, better horizontal visibility of open cup nests due to more open vegetation structure increased predation risk in man–made edges compared to inherent edges. The results suggest that edge–related nest predation is absent or weak in forest dominated landscapes. This may be due to predator types present in the landscape and/or predators habitat use in forest dominated areas. Therefore, it might be that findings documented in other areas, such as in agricultural dominated landscapes, cannot be directly applied to managed forest landscapes.     

Species traits and the response of open‐habitat species to forest edge in landscape mosaics

Human driven changes in land‐use have increased the need to understand how landscape structure affects species distribution. We studied how forest edges affected the distribution of birds in grasslands recently encroached by forest patches. We investigated how species’ biological traits influenced their response to vegetation change near forest edges. We censured birds along 300‐m line transects run into the open habitat perpendicularly to forest edges. We recorded habitat variables and landscape context along each transect and characterized edges and forest patches. We recorded 33 bird species in 153 transects for a total of 654 individuals. We analyzed species response to edges with generalized linear mixed models. Habitat preference was prevalent to explain species response to forest edges. The abundance of open‐habitat birds such as skylark Alauda arvensis decreased significantly in the vicinity of edges. This negative response extended within 150 m from the edge. The effect was disproportionately higher in open‐habitat species with high conservation concern. The abundance of species feeding or/and breeding in both forest and open habitat, such as woodlarks Lullula arborea, sharply increased near edges (positive edge response). Abundance of shrub and non‐shrub dependent species increased with distance to edge. The two species groups did no differ in abundance/distance to edge relationship. Intensity of species response to forest edges varied among transects in relation to transect vegetation characteristics. Edge length or aspect, diet and nest height had no direct effect. We discuss the possible role of variation in resources and nest predation risk to explain observed patterns.     

Adaptive habitat preferences in the Tawny Owl Strix aluco

Capsule: Tawny Owls Strix aluco occupying nest boxes preferred habitats which were positively associated with the probability of nesting success.

Aims: We aimed to determine whether or not: (1) Tawny Owls showed habitat preferences when occupying nest boxes; (2) nesting performance was related to the habitats around occupied nest boxes and (3) habitat availability had changed around available and occupied nest boxes between 1995–2004 and 2005–14.

Methods: Tawny Owls were studied using nest boxes erected in a commercial forest. During nest boxes checks (724 cases), data on occupancy and nesting performance (88 cases) were recorded, and habitat within a 0.4?km radius around nest boxes was analysed.

Results: Tawny Owls had preferences for clearings within forests, mature forests and grasslands but avoided young forests. We found a positive relationship between nesting success and abundance of clearings within the forest, and a negative relationship between nesting success and abundance of young forests. A change in habitat preferences over the two decades was evident, but habitat availabilities remained similar.

Conclusions: Findings indicate adaptive habitat selection in Tawny Owls because preferred habitats were associated with higher fitness and this type of habitat became more frequently selected over time.     

Seasonal habitat-dependent change in nest box occupation by Tengmalm’s owl associated with a corresponding change in nest predation

We investigated the nest-site settlement of the forest-dwelling Tengmalm’s owl (Aegolius funereus) in the temperate zone of Central Europe (Czech Republic) over a 14-year period. We analysed the effect of changes in nest-site suitability (expressed as the proportion of deciduous forest) within the immediate surroundings of the nest boxes (a buffer radius of 25 m) in relation to nest box occupancy, the mean standardized laying date (further the laying date), occurrence of nest predation, and breeding density. In line with the predictions of the site dependence model, we found a positive relationship between the laying date and the proportion of deciduous trees in the nest box surrounding. Further, we found the interactive effect of the laying date and the proportion of deciduous forest surrounding a nest box on the occurrence of breeding attempts predated by pine martens. A higher proportion of deciduous forest was found in the surroundings of predated than non-predated breeding attempts, and a steeper positive relationship between the laying date and the proportion of deciduous forest was found in the surroundings of non-predated than predated breeding attempts. The change in the owls’ habitat utilization can be explained by the process of tree leafing which makes the deciduous forest a less suitable habitat with high risk of nest predation before tree foliage and a more suitable habitat with low risk of nest predation after tree foliage. We conclude that our results are in agreement with the site dependence model, and that the degree of foliage of deciduous forest in the nest surrounding of Tengmalm’s owl is a key factor determining site suitability due to predation risk from pine martens in Central Europe.     

Nest-predation at the edge: an experimental study contrasting two types of edges in the dry Chaco, Paraguay

Forest fragmentation leads to the creation of isolated forest patches with subsequent impact on forest-interior flora and fauna. Forested corridors have been suggested to alleviate some of the impact by increasing the connectivity between remnant forest patches. However, both fragmentation and corridors increase the ratio of edge to core habitat. We studied nest predation of artificial nests at edges between I) contiguous forests and pastures and 2) forested corridors and pastures, in a forest-dominated landscape in the dry Chaco, Paraguay, The aim was lo determine if nest predation was higher near habitat edges compared to within forests and pastures, with special emphasis on edges at forested corridors. We found that predation rates were similar at edges and in interior habitats. Nest predation was higher for both ground and shrub nests in forested areas than in pastures, Predation rates were also higher for both ground and shrub nests at edges along forested corridors compared to edges neighbouring contiguous forests. Forested corridors connecting contiguous forests may thus act as an ecological sink for some species breeding here. Analysis of predator categories revealed that ground nests in pastures were relatively more depredated by mammals and less by birds, compared to both shrub nests in pastures and ground nests in forests.     

Multi-scale turtle dove nest habitat selection in a Mediterranean agroforestry landscape: implications for the conservation of a vulnerable species

Determination of factors affecting nest habitat selection is a major topic in avian ecology, with strong implications for conservation purposes especially for the species with unfavorable status. The turtle dove (Streptopelia turtur) is a vulnerable species that has undergone a rapid and serious decline across its distribution range. I investigated the effect of different variables at two spatial scales (10-m radius, nest site; and 100-m radius, landscape) on the probability of presence of turtle dove nests in an agroforestry system of Central Morocco. Topography, habitat structure, human disturbance, and land use parameters were measured at nests (n?=?70) and random points (n?=?70) at both scales. Generalized linear model analyses showed that, at the nest site scale, tree height best explained occurrence of turtle dove nests (with nest occurring preferentially in smaller trees). At the landscape scale, nest occurrence probability decreased with elevation and distance to the nearest forest edge, and increased with forest cover and distance to the nearest habitation. Comparison of explanatory power of the single-scale models showed that the most relevant scale was the nest site level, followed by landscape scales, but the model including both nest-scale and landscape-scale variables was best. The variation partitioning analysis confirmed this pattern. In study area, the turtle dove nest habitat selection process occurs within a relatively small scale, but the joint effect of variables at the two scales is relevant. From a practical perspective, it would be interesting to reproduce the same experimental approach on other Mediterranean breeding habitats (agricultural and other forest habitats) to find out if this species would adopt the same nest habitat selection pattern.     

Positive edge effects on forest-interior cryptogams in clear-cuts

Biological edge effects are often assessed in high quality focal habitats that are negatively influenced by human-modified low quality matrix habitats. A deeper understanding of the possibilities for positive edge effects in matrix habitats bordering focal habitats (e.g. spillover effects) is, however, essential for enhancing landscape-level resilience to human alterations. We surveyed epixylic (dead wood inhabiting) forest-interior cryptogams (lichens, bryophytes, and fungi) associated with mature old-growth forests in 30 young managed Swedish boreal forest stands bordering a mature forest of high conservation value. In each young stand we registered species occurrences on coarse dead wood in transects 0-50 m from the border between stand types. We quantified the effect of distance from the mature forest on the occurrence of forest-interior species in the young stands, while accounting for local environment and propagule sources. For comparison we also surveyed epixylic open-habitat (associated with open forests) and generalist cryptogams. Species composition of epixylic cryptogams in young stands differed with distance from the mature forest: the frequency of occurrence of forest-interior species decreased with increasing distance whereas it increased for open-habitat species. Generalists were unaffected by distance. Epixylic, boreal forest-interior cryptogams do occur in matrix habitats such as clear-cuts. In addition, they are associated with the matrix edge because of a favourable microclimate closer to the mature forest on southern matrix edges. Retention and creation of dead wood in clear-cuts along the edges to focal habitats is a feasible way to enhance the long-term persistence of epixylic habitat specialists in fragmented landscapes. The proposed management measures should be performed in the whole stand as it matures, since microclimatic edge effects diminish as the matrix habitat matures. We argue that management that aims to increase habitat quality in matrix habitats bordering focal habitats should increase the probability of long-term persistence of habitat specialists.     

Characteristics of Mount Graham Red Squirrel Nest Sites in a Mixed Conifer Forest

Abstract: The Mount Graham red squirrel (Tamiasciurus hudsonicus grahamensis) is constrained to the Pinaleño Mountains in southeastern Arizona, USA. The population's endangered status and extensive forest damage from insects and fire warrants a better understanding of habitat variables important for nest site selection. We examined characteristics of cavity (n = 91) and drey (n = 38) nests and compared these to random sites (n = 113). Dreys were found primarily in Engelmann spruce (Picea engelmannii) and corkbark fir (Abies lasiocarpa var. arizonica). Cavity nests occurred primarily in aspen (Populus tremuloides) and corkbark fir. Squirrels selected nest sites with higher canopy cover and more corkbark fir, decayed logs, and living trees. Forest management plans emphasizing thinning must consider how altering these habitat characteristics could affect availability and suitability of tree stands for nesting squirrels.     

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.     

On the edge: habitat restoration priorities for three critically endangered bird species on Sangihe,Indonesia

Remnant forests on the small Wallacean island of Sangihe north of Sulawesi hold the entire ranges of more critically endangered (CR) bird species than any other comparable area on earth. We develop habitat association models for three of these CR species to identify critical habitat features as well as areas where habitat falls slightly short of suitability, and to determine whether another area of forest away from the largest block might be suitable as an insurance site for a translocated population. Hopes for all three species appear almost totally pinned to forest within a 13 km² area of the Sahendaruman crater, with virtually no near-suitable habitat away from this site. There is, however, little overlap in habitats between one CR species and the other two: cerulean flycatcher Eutrichomyias rowleyi is associated with mature streamside forest with full canopy cover, lianas, and mid-level growth, while Sangihe whistler Coracornis sanghirensis and Sangihe golden bulbul Hypsipetes platenae are restricted to ridgetop forest with full canopy cover and large trees. We pinpoint small areas (around 5 km²) of forest in the crater that are already suitable or can be made so with habitat management, and these are absolute priorities for conservation action. We show how habitat characteristics identified within models might be enhanced, and how features, especially certain tree species, can be used as indicators of future habitat improvement.     

Distance from riparian edge reduces brood parasitism of southwestern willow flycatchers,whereas parasitism increases nest predation risk

The southwestern willow flycatcher (Empidonax traillii extimus) is a federally endangered subspecies that breeds in increasingly fragmented and threatened habitat. We examined whether temporal and habitat characteristics were associated with risk of predation and probability of brood parasitism by brown-headed cowbirds (Molothrus ater) on flycatcher nests at 6 sites in southern Nevada and northwestern Arizona, USA. For nest predation, we found the most support for a model that included date and an interaction between parasitism status and nesting stage. Daily nest survival decreased from 0.87 (95% CI = 0.81–0.93) to 0.78 (95% CI = 0.72–0.84) through the season for parasitized nests but remained relatively constant for unparasitized nests (0.93, 95% CI = 0.91–0.95 to 0.92, 95% CI = 0.91–93). Parasitized nests had lower survival than non-parasitized nests during the incubation (0.85, 95% CI = 0.84–0.86 vs. 0.92, CI = 0.91–0.93) and nestling (0.79, 95% CI = 0.77–0.81 vs. 0.91, 95% CI = 0.90–0.92) stages. Of the variables included in our parasitism candidate models, model-averaged coefficients and odds ratios supported only distance to habitat edge; odds of parasitism decreased 1% for every 1 m from the habitat edge. Nests greater than 100 m from an edge were 50% less likely to be parasitized as those on an edge, however, only 52 of 233 nests (22%) were found at this distance. Where management and conservation goals include reducing nest losses due to parasitism, we recommend restoration of habitat patches that minimize edge and maximize breeding habitat further from edges. At sites where cowbirds have been documented as important nest predators, controlling cowbirds may be one option, but further study of the link between parasitism and nest predation and the identification of major nest predators at specific sites is warranted. © 2011 The Wildlife Society.     

Nesting success in Redshank Tringa totanus breeding on coastal meadows and the importance of habitat features used as perches by avian predators

Capsule Nest survival rates could not be explained by distance to habitat edges or other features used by predators.

Aims To investigate if predation on Redshank nests was affected by habitat characteristics at a local scale.

Methods We examined survival rates of Redshank nests on coastal meadows on the Baltic island of Gotland, Sweden, over two breeding seasons. We analysed nest survival rates in relation to several habitat characteristics that may benefit predators searching for nests. We examined existing studies concerning predation rates on wader nests in relation to edges and habitat features potentially used by avian predators.

Results We found no significant effects of distance to habitat edge or to nearest potential lookout for avian predators or to shoreline. Abundance of Lapwings Vanellus vanellus, an aggressive species with active nest-defence, did not have any significant effect on nest survival rate, nor did vegetation concealment of nests. Nest survival rates were significantly different between years and lower later in the season.

Conclusions There is only weak support for general effects on wader nest predation rates of proximity to edges and features used by avian predators. Simple mechanical management actions such as removal of trees and bushes on coastal meadows may not directly, and by itself, result in higher reproductive success of waders. Further understanding is needed of the behaviour of predators and the composition of the predator community in different landscapes in order to increase the efficiency of management actions to remove threats to vulnerable species on coastal meadows.     

Forest Management Considerations for Conservation of Black Woodpecker Dryocopus martius and White-backed Woodpecker Dendrocopos leucotos Populations in Quinto Real (Spanish Western Pyrenees)

The woodlands of Quinto Real (Quinto Real, Erreguerena and Legua Acotada) are a 3,000 hectare beech (Fagus sylvatica) forest managed by the shelterwood system applied to even-aged (regular) stands. This study analyses how forest management determines the local distribution of the white-backed woodpecker (Dendrocopos leucotos) and black woodpecker (Dryocopus martius) and its relationship with the type, structure and size of the stands used for nesting by both species, as well as their dead wood requirements. The most suitable nesting habitat of both species is the mature forest (stands of regular large final crop trees), but the size of the mature fragments and a minimum quantity of dead wood is also important.     

扎龙保护区人工林内中华攀雀巢址特征分析

作者2011年9 ～ 10月在黑龙江省扎龙国家级自然保护区对人工林内中华攀雀(Remiz consobrinus)的巢址特征进行了研究.研究期间共发现36巢,选取巢距地面距离、巢距主干距离、巢距挂枝末端距离、巢树胸径等9个巢址因子进行主成分分析.结果表明,巢下生境、巢距地面距离和巢距主干距离以及巢距挂枝末端距离在中华攀雀巢址选择中起主要作用;巢树胸径、巢向和巢挂枝年龄次之.中华攀雀巢距地面(5.59±1.44)m,距主干距离为(1.81±0.50)m,距挂枝末段距离为(0.10±0.04)m,巢树胸径(0.29±0.08)m.巢距地面高度(P =0.002 3)和巢距明水面距离(P =0.003 7)在芦苇沼泽与林地草甸2种生境类型之间差异显著,巢树胸径在林地草甸与房屋农田2种生境类型之间差异显著(P=0.003 4),不同生境类型之间巢距主干距离、巢距挂枝末端距离和巢挂枝年龄无显著差异.     

Nest habitat selection by the Austral parakeet in north‐western Patagonia

Identifying habitat or nesting microhabitat variables associated with high levels of nest success is important to understand nest site preferences and bird–habitat relationships. Little is known about cavity availability and nest site requirements of cavity nesters in southern hemisphere temperate forests, although nest site limitation is suggested. Here we ask which characteristics are selected by the Austral parakeet (Enicognathus ferrugineus) for nesting in Araucaria araucana–Nothofagus pumilio forest in Argentine Patagonia. We compared nest plot and tree characteristics with unused plots and trees among areas of different A. araucana–N. pumilio density. We also examine whether nest plot and tree use and selection, and the associated consequences for fitness of Austral parakeets are spatially related to forest composition. Austral parakeets showed selectivity for nests at different spatial scales, consistently choosing isolated live and large trees with particular nest features in a non‐random way from available cavities. Mixed A. araucana–N. pumilio forests are ideal habitat for the Austral parakeets of northern Patagonia, offering numerous potential cavities, mainly in N. pumilio. We argue that Austral parakeet reproduction and fitness is currently very unlikely to be limited by cavity availability, although this situation may be rapidly changing. Natural and human disturbances are modifying south temperate forests with even‐aged mid‐successional stands replacing old growth forests. Cavity nesting species use and need old growth forests, due to the abundance of cavities in large trees and the abundance of larvae in old wood. Neither of the latter resources is sufficiently abundant in mid‐successional forests, increasing the vulnerability and threatening the survival of the Austral.     

Nest site selection in middle and great spotted woodpeckers <Emphasis Type="Italic">Dendrocopos medius</Emphasis> &; <Emphasis Type="Italic">D. major</Emphasis>: implications for forest management and conservation

Success of species conservation depends to a large extent on comprehensive management that considers all critical aspects of a species’ niche. Many studies have examined habitat factors in relation to occurrence, abundance or foraging behaviour of European woodpecker species, while relatively little is known about nest site selection. I compared habitat structures used for nesting by middle and great spotted woodpeckers Dendrocopos medius and D. major with available structures in an oak forest in the Swiss lowlands. I first tested if nest trees were randomly selected among available trees by focusing on species, condition and diameter of nest trees, and on the presence of the fruiting body (hereafter sporophore) of polypores (wood-decomposing fungi). Second, I examined if the nesting niches of the two species were differentiated. Both species showed strong preferences for oaks, large trees, dead trees and for trees with sporophores. Nest sites of the two species differed most strongly with respect to the presence of sporophores, cavity age and tree condition, pointing towards interspecific competition for nest sites. Old living or dead trees with sporophores are central components of the nesting niche of middle and great spotted woodpeckers. Conservation plans for the threatened middle spotted woodpecker have so far mostly focused on the needs in terms of distribution and foraging; future conservation strategies and forest management must take into account the preference for dead and decaying trees with sporophores as another vital resource. This will also provide benefits for other woodpecker species as well as for the community of secondary cavity nesters.