Drivers of low breeding success in the Lesser Spotted Woodpecker Dendrocopos minor in England: testing hypotheses for the decline

Capsule The breeding success of Lesser Spotted Woodpeckers Dendrocopos minor is now lower in England than previously reported and also lower than found in studies elsewhere in Europe.

Aims To quantify the breeding success and identify the causes of nest failure. To test the hypotheses that breeding success is related to aspects of food limitation and parental care, and inclement weather during the nesting period, or to interactions with Great Spotted Woodpeckers.

Methods Nests were monitored in three regions of England, recording survival and causes of failure. We measured aspects of food limitation and parental care, rainfall and Great Spotted Woodpecker interactions at nests, to explore whether there was any evidence that these factors were related to breeding success. We compared results to other studies from the UK and continental Europe.

Results Nest survival was 52%. The average number of chicks produced from successful nests was 2.8. Chick-stage daily nest survival was positively related to provisioning rates, indicating that food supply may be limiting. The most common cause of nest failure was presumed starvation of chicks after the disappearance of an adult. Some females ceased visiting nests, leaving provisioning solely to the male. This behaviour has been reported elsewhere in Europe, but in the present study males were unable to compensate fully by increasing their provisioning rates, leading to poor nest survival. Provisioning rates and chick-stage daily nest survival were negatively associated with rainfall. Nest predation by Great Spotted Woodpeckers occurred but was a less frequent cause of failure. Aggressive interactions were recorded between the two woodpecker species but these were unrelated to breeding parameters.

Conclusions Low breeding success is most probably related to food shortages in the breeding period. Simple population modelling using parameters from the present study and from published work shows that if the low productivity that we have observed is replicated throughout Britain, it would be sufficient to account for the observed population decline. However, the possibility that survival rates are also low cannot be ruled out.     

Factors influencing the nesting success of Lapwings Vanellus vanellus and behaviour of Red Fox Vulpes vulpes in Lapwing nesting sites

Capsule Lapwing nest predation was negatively correlated to nest density, while Lapwing alarm duration in response to foxes was positively correlated with the number of Lapwing broods present.

Aims To identify factors affecting Lapwing nest predation and Red Fox search effort.

Methods Lapwing nest success was monitored at four sites in 1996, seven sites in 1997 and six sites in 1998. In 1997 we mapped the position of all Lapwing nests in order to determine distances between nests, and the proximity of linear features and potential avian predator perches to each nest. From April to June 1998 we carried out 199 hours of nocturnal observations at six Lapwing nesting sites using night vision equipment.

Results The risk of nest predation was significantly higher for more isolated nests. Nocturnal observations showed that of all the nocturnal predators, foxes were the most active at Lapwing nesting sites. However, fox search effort in Lapwing colonies was relatively low, averaging 57 s/ha per visit. Foxes spent significantly longer foraging near breeding Lapwings (measured as duration of alarm calls) when more broods were present. Fox search effort (s/ha per hour of observation) tended to be greater in areas of high waterbird density.

Conclusion The lack of positive density-dependent nest predation, the relatively low search effort of foxes near Lapwing nesting sites and the high nest success sometimes achieved in areas with foxes all suggest that Lapwing nest predation by foxes is ‘incidental’. Lapwing chicks are probably more vulnerable to predation by foxes than clutches.     

Associations between distance to forest and spatial and temporal variation in abundance of key peatland breeding bird species

Capsule Negative forest edge effects were detected for Willow Ptarmigan (Red Grouse) Lagopus lagopus and Dunlin Calidris alpina.

Aims To investigate the effects of distance to forest on the abundance and changes in abundance of four key peatland breeding bird species, and to measure changes in predatory bird numbers, in the peatlands of northern Scotland.

Methods Bird surveys were carried out in 2000 at 34 plots, covering 197 km² of peatland, and 80 forestry point‐count sites, first surveyed in 1988. Habitat data were also collected in 2000. We used multi‐model inference to investigate the associations between forest distance and other habitat variables, and the abundance, and changes in abundance, of four bird species of economic or conservation importance: Red Grouse, European Golden Plover Pluvialis apricaria, Dunlin and Common Greenshank Tringa nebularia.

Results There was strong evidence that distance to forest was negatively associated with Dunlin abundance and changes in Red Grouse abundance, but only weak evidence for negative associations with Golden Plover abundance and changes in Dunlin abundance. There was no evidence of a forest distance effect on Greenshank. Among predatory birds, there were no significant increases either on peatland plots or in new forestry plantations.

Conclusions This study provides evidence that, for a given habitat quality, Dunlin densities are lower, and Red Grouse declines more likely, near to forest edges, but weak evidence only that Dunlin declines are more likely, and Golden Plover abundance lower, near to forests. These results suggest that for at least two key peatland breeding birds, forest removal is likely to benefit birds breeding on adjacent unafforested peatland.     

Vegetation structure influences predation rates of early nests in subarctic breeding waders

Ground-nesting species are vulnerable to a wide range of predators and often experience very high levels of nest predation. Strategies to reduce nest vulnerability can include concealing nests in vegetation and/or nesting in locations in which nests and eggs are camouflaged and less easy for predators to locate. These strategies could have important implications for the distribution of ground-nesting species and the success rates of nests in areas with differing vegetation structure. However, the factors influencing the success of nest concealment and camouflage strategies in ground-nesting species are complex. Here we explore the effects of local vegetation structure and extent of nest concealment on nest predation rates in a range of ground-nesting, sympatric wader species with differing nest concealment strategies (open-nest species: Oystercatcher Haematopus ostralegus, Golden Plover Pluvialis apricaria and Whimbrel Numenius phaeopus; concealed-nest species: Black-tailed Godwit Limosa limosa, Redshank Tringa totanus and Snipe Gallinago gallinago) in south Iceland, in landscapes that comprise substantial variability in vegetation structure at a range of scales. We monitored 469 nests of these six wader species in 2015 and 2016 and ~40% of these nests were predated. Nest predation rates were similar for open-nest and concealed-nest species and did not vary with vegetation structure in the surrounding landscape, but nest-concealing species were ~10% more likely to have nests predated when they were poorly concealed, and the frequency of poorly concealed nests was higher in colder conditions at the start of the breeding season. For concealed-nest species, the reduced capacity to hide nests in colder conditions is likely to reflect low rates of vegetation growth in such conditions. The ongoing trend for warmer springs at subarctic latitudes could result in more rapid vegetation growth, with consequent increases in the success rates of early nests of concealed-nest species. Temperature-related effects on nest concealment from predators could thus be an important mechanism through which climate change affecting vegetation could have population-level impacts on breeding birds at higher latitudes.     

Herbaceous ground cover reduces nest predation in olive groves

Capsule Bare ground increases artificial nest predation in olive groves.

Aims To assess the effect of different soil management regimes on nest predation rates in olive groves.

Methods We performed nest predation experiments with artificial nests during the breeding season in 2013, in two areas of southern Spain. Each artificial nest (n?=?300) contained three quail Coturnix eggs, two of which were unmanipulated and the third one was emptied and injected with plaster. Predators were identified by marks on eggs filled with plaster.

Results Ground nests were significantly more depredated, irrespective of the presence of ground cover; tree nests were less depredated in fields with ground cover. There was a clear difference in nest predators of ground and tree nests. Rodents were the most frequent predators of tree nests.

Conclusion Lower predation rates of tree nests in orchards with ground cover are probably linked to a change in the foraging behaviour of rodents, which in these more complex habitats might be restricted by rodents' own risk of predation. This study underscores the important role of agricultural practices in preserving farmland bird communities, particularly tree-nesting species, suggesting that for this group, implementation of ground cover in olive groves might enhance breeding success by reducing nest predation rates.     

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.     

Week-end bias at observatories

Capsule Although subject to human disturbance Turtle Doves do nest successfully in these olive and orange orchards.

Aim To investigate the breeding ecology of Turtle Doves in a man‐made agricultural habitat in central Morocco.

Methods Turtle Dove nests were monitored in orange and olive orchards over three years (2006, 2007 and 2008). Nest abundance, nest location, egg‐laying chronology, clutch size, nest survival rates and breeding success were determined and compared between orchard types.

Results The Moroccan population of Turtle Doves start breeding earlier than European populations. Clutch size, nest survival rates and breeding success were similar in orange and olive orchards. Nest location differed between orange and olive trees. Nest densities were 16 nests/ha in olive orchards and 45 nests/ha in orange orchards. Nest success rate averaged 48%. Daily nest survival rates did not vary according to orchard types, year and date. In the two orchards, no nest position variables were significant predictors of nesting success.

Conclusion Although highly frequented by people, fruit orchards seem to be suitable breeding habitats for Turtle Doves in this region.     

Diversionary feeding and nestling diet of Hen Harriers Circus cyaneus

Capsule: Diversionary feeding reduced Hen Harrier Circus cyaneus nestlings’ natural food intake by half. Red Grouse Lagopus lagopus scotica chicks constituted 0–4% of all nestling food items. Annually, this reduced annual grouse chick production by 0–6%.

Aim: To quantify proportions of diversionary and natural food (including grouse) delivered to Hen Harrier nestlings in relation to brood size, male status and natural prey abundance.

Methods: We recorded diversionary food provisioned to 25 Hen Harrier broods (2008–15) and studied the diet of 15 broods using observations from hides, nest cameras and regurgitated pellet analysis. Variation in nestling diet was analysed using compositional analysis.

Results: Hen Harriers took 76% of diversionary food provided. Depending on assessment method, average nestling diet was 44–53% diversionary food, 39–55% natural prey (including 24–45% passerines, 4–15% small mammals, 0–4% grouse chicks) and 0–9% unknown items. The amount of diversionary food consumed was not influenced by male status, brood size or natural prey abundance. The number of Red Grouse chicks delivered annually was 34–100% lower than expected under unfed conditions, however, the confidence intervals associated with these estimates were large.

Conclusion: Diversionary food influenced Hen Harrier nestling diet and reduced the number of Red Grouse chicks taken relative to modelled predictions. It may help reduce conflict between Hen Harrier conservation and Red Grouse shooting, but only if overall grouse productivity is thereby maintained or increased.     

The influence of survey frequency on population estimates of moorland breeding birds

Capsule A minimum of four constant‐effort‐search survey visits are required to generate reliable population estimates of breeding birds on moorland that are not subject to biases associated with varying levels of detectability through the season.

Aims To investigate the influence of the number and the combination of survey visits on the population estimates of breeding birds on moorland.

Methods Four constant‐effort‐search surveys (80–100 minutes per km² per visit) of moorland in southwest Scotland were undertaken in each of six years, 2003–2008. Using standard protocols, the numbers of apparent territories that would have been identified for each possible combination of survey visits were determined.glms were used to assess the influence of the frequency of survey visits, and different combination scenarios on the derived population estimates for Red Grouse, European Golden Plover, Common Snipe, Eurasian Curlew, Sky Lark, Winter Wren and Stonechat. Independent assessments of population density were made by transect sampling for Red Grouse and Sky Lark.

Results Robust population estimates were possible from three survey visits for European Golden Plover, Eurasian Curlew and Stonechat. However, there were differences between species in the seasonal variation of their detectability. Four survey visits would underestimate the populations of Red Grouse (probably by 67–91%), Sky Lark (probably by 31–61%) and Winter Wren (by an undetermined proportion). Common Snipe were also likely to be underestimated after four survey visits, but the value of the derived estimate as an index of population density deserves further investigation.

Conclusions If there is a need to carry out a multi‐species survey on moorland, we suggest that a minimum of four survey visits is required to ensure the derivation of reliable population estimates for a suite of the most readily detectable species. Population estimates derived from three or fewer survey visits risk biases through uneven sampling in periods of differing detectability. With evidence for changes in the breeding phenology of birds associated with changing climate or weather patterns, it arguably becomes more important to ensure that surveys sample an adequately broad period of the breeding season.     

Predators of Spotted Flycatcher Muscicapa striata nests in southern England as determined by digital nest-cameras

Capsule Avian predators are principally responsible.

Aims To document the fate of Spotted Flycatcher nests and to identify the species responsible for nest predation.

Methods During 2005–06, purpose-built, remote, digital nest-cameras were deployed at 65 out of 141 Spotted Flycatcher nests monitored in two study areas, one in south Devon and the second on the border of Bedfordshire and Cambridgeshire.

Results Of the 141 nests monitored, 90 were successful (non-camera nests, 49 out of 76 successful, camera nests, 41 out of 65). Fate was determined for 63 of the 65 nests monitored by camera, with 20 predation events documented, all of which occurred during daylight hours. Avian predators carried out 17 of the 20 predations, with the principal nest predator identified as Eurasian Jay Garrulus glandarius. The only mammal recorded predating nests was the Domestic Cat Felis catus, the study therefore providing no evidence that Grey Squirrels Sciurus carolinensis are an important predator of Spotted Flycatcher nests. There was no evidence of differences in nest survival rates at nests with and without cameras. Nest remains following predation events gave little clue as to the identity of the predator species responsible.

Conclusions Nest-cameras can be useful tools in the identification of nest predators, and may be deployed with no subsequent effect on nest survival. The majority of predation of Spotted Flycatcher nests in this study was by avian predators, principally the Jay. There was little evidence of predation by mammalian predators. Identification of specific nest predators enhances studies of breeding productivity and predation risk.     

Mortality of Wood Warbler Phylloscopus sibilatrix nests in Welsh Oakwoods: predation rates and the identification of nest predators using miniature nest cameras

Capsule Predation was the main cause of nest failure, but predation rates have remained unchanged since the 1980s. Eurasian Jays Garrullus glandarius were the most common predator.

Aims To quantify, and compare, nest predation rates for 1982–84 and 2009–11, and to identify predators of Wood Warbler Phylloscopus sibilatrix nests in Welsh oakwoods.

Methods During 2009–11, 167 Wood Warbler nests were monitored and purpose-built miniature nest cameras deployed at 73 of them. Nest predation rates were compared with 67 nests monitored during 1982–84.

Results Of 167 nests monitored from 2009 to 2011, 62 failed due to predation (32/73 camera nests, 30/94 non-camera nests), giving an overall Daily Survival Rate (DSR?±?se) of 0.979?±?0.003. This was not significantly different from the rate during 1982–84 (0.967?±?0.006). In 2009–11, the DSR of nests declined temporally during the season at both the egg and chick stages. For chick stage nests, DSR varied annually and nonlinearly with age of nestlings. There was no evidence for an effect of cameras at either stage. Of 32 camera nests lost to predation, the predator was identified from 28, resulting in 30 predators being identified. There was one case of multiple predators at a single nest. The majority of nest predation was carried out by birds (28/30), predominantly Eurasian Jays (18/28), but also Common Buzzards Buteo buteo (5/28), Great Spotted Woodpeckers Dendrocopos major (3/28) and Eurasian Sparrowhawks Accipiter nisus (2/28). There was one predation by both a Eurasian Badger Meles meles and a Red Fox Vulpes vulpes. There were no records of Grey Squirrels Sciurus carolinensis depredating nests.

Conclusions Nest predation rates were similar in both periods, suggesting that increased rates of nest predation have not been driving the decline of the Wood Warbler population in Wales. Deployment of nest cameras did not affect nest survival rates and were successful in identifying nest predators, the majority of which were avian, especially Eurasian Jays. Knowledge of the identity of nest predators can aid the development of conservation measures.     

DO NEST SITE CHARACTERISTICS AFFECT THE BREEDING SUCCESS OF RED BISHOPS EUPLECTES ORIX?

Summary

Ferguson, J.W.H. 1994. Do nest site characteristics affect the breeding success of Red Bishops Euplectes orix? Ostrich 65:274-280.

A colony of Red Bishop birds Euplectes orix in a reed bed near Pretoria was studied during two breeding seasons. Breeding activity was greater during the second year, following increased rainfall. Predation was the most important source of mortality with 25–30% of the nests yielding fledglings. Between 7 and 11% of the nests were parasitised by Diederik Cuckoos. Reed height and distance from the edge of the reed bed were strongly correlated with nest density. From a temporal perspective breeding success was highest in late January following the peak in breeding activity. These observations suggest that overall breeding success is higher when nest densities are low. The mean fledging rate per nest was lower in areas of high nest density. This was, however, a statistical artifact. Multivariate analyses could not identify any environmental factors as predictors of breeding success within a colony.     

Nest-site selection and characteristics in a mixed-species colony of Avocets Recurvirostra avosetta and Black-winged Stilts Himantopus himantopus

Capsule Causes of breeding failure determined optimal nest location, Black-winged Stilts being better adapted than Avocets to nest close to water.

Aims To compare nest size and location between the two species and to test whether there were inter-species differences that might suggest specific nesting adaptations, and to investigate possible correlates between hatching success and nest location.

Methods Nest-site selection, characteristics and hatching success were studied during 1989 in a large mixed-species colony located in southern Spain.

Results Black-winged Stilt nests differed in composition and size depending on distance to water (nests touching the water were larger and included mud), but Avocet nests did not. Avocets nests were more aggregated and central within the colony than those of Black-winged Stilts. Causes of breeding failure were flooding and rat predation. Successful or unsuccessful Black-winged Stilt nests did not differ significantly in characteristics or location. Successful Avocet nests were further from water than flooded nests and further from dry land than depredated ones. Distance to the centre of the colony did not affect hatching success.

Conclusion Black-winged Stilts were better adapted than Avocets to nest near water, due to their greater plasticity in nest-building behaviour. Causes of breeding failure determined optimal nest location.     

Do seasonal patterns of rat snake (Pantherophis obsoletus) and black racer (Coluber constrictor) activity predict avian nest predation?

Avian nest success often varies seasonally and because predation is the primary cause of nest failure, seasonal variation in predator activity has been hypothesized to explain seasonal variation in nest success. Despite the fact that nest predator communities are often diverse, recent evidence from studies of snakes that are nest predators has lent some support to the link between snake activity and nest predation. However, the strength of the relationship has varied among studies. Explaining this variation is difficult, because none of these studies directly identified nest predators, the link between predator activity and nest survival was inferred. To address this knowledge gap, we examined seasonal variation in daily survival rates of 463 bird nests (of 17 bird species) and used cameras to document predator identity at 137 nests. We simultaneously quantified seasonal activity patterns of two local snake species (N = 30 individuals) using manual (2136 snake locations) and automated (89,165 movements detected) radiotelemetry. Rat snakes (Pantherophis obsoletus), the dominant snake predator at the site (~28% of observed nest predations), were most active in late May and early June, a pattern reported elsewhere for this species. When analyzing all monitored nests, we found no link between nest predation and seasonal activity of rat snakes. When analyzing only nests with known predator identities (filmed nests), however, we found that rat snakes were more likely to prey on nests during periods when they were moving the greatest distances. Similarly, analyses of all monitored nests indicated that nest survival was not linked to racer activity patterns, but racer‐specific predation (N = 17 nests) of filmed nests was higher when racers were moving the greatest distances. Our results suggest that the activity of predators may be associated with higher predation rates by those predators, but that those effects can be difficult to detect when nest predator communities are diverse and predator identities are not known. Additionally, our results suggest that hand‐tracking of snakes provides a reliable indicator of predator activity that may be more indicative of foraging behavior than movement frequency provided by automated telemetry systems.     

The direct and indirect effects of predation by Hen Harriers Circus cyaneus on trends in breeding birds on a Scottish grouse moor

Two phases of an experimental reduction in management at Langholm Moor in southwest Scotland provided an insight into factors that determined trends in the abundance of moorland birds. In 1992 the historical control of breeding Hen Harriers Circus cyaneus stopped and in 2000 grouse moor management was discontinued. Golden Plover Pluvialis apricaria , Lapwing Vanellus vanellus , Curlew Numenius arquata and Red Grouse Lagopus lagopus scoticus declined, whilst Carrion Crow Corvus corone and Snipe Gallinago gallinago increased. Hen Harriers increased from two to 20 breeding females, then declined back to two. Lapwing abundance was positively associated with that of Hen Harriers, and moorland passerines (Skylark Alauda arvensis , Meadow Pipit Anthus pratensis and Stonechat Saxicola torquata ) were negatively associated. Golden Plover, Lapwing, Curlew, Red Grouse, Skylark and Hen Harrier were more abundant when the moor was managed for grouse, whilst Carrion Crow, a common predator of clutches of ground-nesting birds, increased during the second half when management ceased. Increased Crow numbers, together with an increase in Red Foxes Vulpes vulpes , probably contributed to the observed bird declines.     

Blue penguin (Eudyptula minor) nest distribution and breeding success on Otago Peninsula, 1992 to 1998

Abstract

Annual counts of nests with eggs or chicks (known nests) were made at blue penguin (Eudyptula minor) breeding sites on the Otago Peninsula in each November from 1994 to 1997. Although the population has doubled to an estimated 600 known nests over this period, the number of breeding sites on the Otago Peninsula has reduced since the 1970s. Breeding success at three areas at Taiaroa Head were monitored by regular nest checks in the breeding season from 1992 to 1998. At Taiaroa Head reproductive success ranged from 41 to 78% at the three sites during the seven‐year study and was generally higher for pairs nesting in nest boxes than for those in burrows. The percentage of breeding pairs that laid a second clutch after fledging at least one chick from their first clutch (double brooded) varied between seasons (0–48%) and was correlated with the date of the onset of breeding. Egg loss, possibly through predation by Norway rats (Rattus norvegicus), influenced the significantly lower reproductive success at one area (Area A) at Taiaroa Head during the 1996 season.     

No evidence for observer effects on Lark Sparrow nest survival

ABSTRACT Methods for monitoring bird nests might influence rates of nest predation, but the effects of various methods (e.g., visual markers and observer visitation rates) are often separately investigated among disparate avian taxa and geographic regions. Few investigators have explored the potential effects observers might have on nest success of grassland birds, despite concerns regarding population declines of these species in North America. We examined the possible effects of three monitoring techniques on daily nest survival of Lark Sparrows (Chondestes grammacus): (1) presence or absence of visible markers near nests, (2) observer visitation frequency, and (3) presence or absence of data loggers in nests. We monitored 113 Lark Sparrow nests during the 2009 breeding season. Of these nests, 88.5% failed due to predation, abandonment, weather, or unknown causes, yielding an overall nest success estimate of 9.8% based on daily survival estimation. Main effects of each monitoring technique appeared in top (ΔAICc <2) logistic exposure models. However, 95% confidence intervals around parameter estimates for each technique included zero, indicating no significant effects on daily nest survival. Our results suggest that the nest‐monitoring techniques we used had no effect on Lark Sparrow nest success and, if true, nest survival of other songbirds in arid grasslands of the Great Plains may also be unaffected by cautious nest monitoring. However, we cannot rule out the possibility that any effects of the various techniques in our study were masked by locally intense nest predation. Therefore, additional study is needed to determine if there may be observable variation in nest survival among various nest‐monitoring treatments in other areas of the southern Great Plains where nest predation is less frequent.     

Predation on artificial and natural nests in the lowland rainforest of Papua New Guinea

Capsule: Although survival of nests was similar between forest fragments and continuous forest, the range of predators differed. Artificial nests provide an under-estimate of nest predation by snakes.

Aims: To estimate the natural nest predation rate in continuous primary forest, compare it with predation rates in forest fragments. To assess the reliability of nest survival rates determined by the use of artificial nests with clay eggs and identify the main nest predators.

Methods: We observed survival of natural nests during the incubation period in continuous primary forest in Papua New Guinea. Some nests were monitored with infrared cameras. We also used artificial nests deployed with clay eggs to identify predators.

Results: There was a predation rate of 50% for natural nests and snakes were major predators of nest contents. Clutch daily survival rates (DSRs) differed among nest types. The DSR of artificial nests (0.977) was not significantly different to that of natural cup nests (0.969). Survival rates of artificial nests were similar in forest fragments and continuous forest. Forest fragments had, however, a higher proportion of avian predators than continuous forest.

Conclusion: Although, we observed similar survival rates in artificial and natural nests, the composition of nest predators was different between natural and artificial nests. Artificial nests were not suitable for estimating the real predation caused by reptiles. Nevertheless, we find that participation of avian nest predators can be estimated correctly with the use of artificial nests.     

Predators of Greater Sage‐Grouse nests identified by video monitoring

ABSTRACT Nest predation is the primary cause of nest failure for Greater Sage‐Grouse (Centrocercus urophasianus), but the identity of their nest predators is often uncertain. Confirming the identity of these predators may be useful in enhancing management strategies designed to increase nest success. From 2002 to 2005, we monitored 87 Greater Sage‐Grouse nests (camera, N= 55; no camera, N= 32) in northeastern Nevada and south‐central Idaho and identified predators at 17 nests, with Common Ravens (Corvus corax) preying on eggs at 10 nests and American badgers (Taxidea taxis) at seven. Rodents were frequently observed at grouse nests, but did not prey on grouse eggs. Because sign left by ravens and badgers was often indistinguishable following nest predation, identifying nest predators based on egg removal, the presence of egg shells, or other sign was not possible. Most predation occurred when females were on nests. Active nest defense by grouse was rare and always unsuccessful. Continuous video monitoring of Sage‐Grouse nests permitted unambiguous identification of nest predators. Additional monitoring studies could help improve our understanding of the causes of Sage‐Grouse nest failure in the face of land‐use changes in the Intermountain West.