Experimental enlargement of nest size does not increase risk of predation or brood parasitism in the Great Reed Warbler Acrocephalus arundinaceus

We assessed whether nest size affects the probability of nest loss using dyads of large and small (large being twice the size of small) inactive Great Reed Warbler Acrocephalus arundinaceus nests placed at similar sites in Great Reed Warbler territories. Large nests were not predated significantly more frequently than small nests. Experimentally enlarged active Great Reed Warbler nests suffered non‐significantly higher predation compared with non‐manipulated control nests. Our experiments did not support the nest‐size hypothesis and suggested that nest size does not appear to be a factor affecting the risk of nest predation in this species. The probability of brood parasitism by the Common Cuckoo Cuculus canorus was also unaffected by experimental nest enlargement, supporting the commonly accepted hypothesis that the Common Cuckoo searches for suitable host nests by host activity during nest building rather than nest size.     

Effects of nest-site characteristics and parental activity on cowbird parasitism and nest predation in Brown-and-yellow Marshbirds

ABSTRACT Nest‐site selection and nest defense are strategies for reducing the costs of brood parasitism and nest predation, two selective forces that can influence avian nesting success and fitness. During 2001–2002, we analyzed the effect of nest‐site characteristics, nesting pattern, and parental activity on nest predation and brood parasitism by cowbirds (Molothrus spp.) in a population of Brown‐and‐yellow Marshbirds (Pseudoleistes virescens) in the Buenos Aires province, Argentina. We examined the possible effects of nest detectability, nest accessibility, and nest defense on rates of parasitism and nest predation. We also compared rates of parasitism and nest predation and nest survival time of marshbird nests during the egg stage (active nests) with those of the same nests artificially baited with passerine eggs after young fledged or nests failed (experimental nests). Most nests (45 of 48, or 94%) found during the building or laying stages were parasitized, and 79% suffered at least one egg‐predation event. Cowbirds were responsible for most egg predation, with 82 of 107 (77%) egg‐predation events corresponding to eggs punctured by cowbirds. Nests built in thistles had higher rates of parasitism and egg predation than nests in other plant, probably because cowbirds were most active in the area where thistles were almost the only available nesting substrate. Parasitism rates also tended to increase as the distance to conspecific nests increased, possibly due to cooperative mobbing and parental defense by marshbirds. The proportion of nests discovered by cowbirds was higher for active (95%) than for experimental (29%) nests, suggesting that cowbirds used host parental activity to locate nests. Despite active nest defense, parental activity did not affect either predation rates or nest‐survival time. Thus, although nest defense by Brown‐and‐yellow Marshbirds appears to be based on cooperative group defense, such behavior did not reduce the impact of brood parasites and predators.     

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.     

Predation of Lapwing Vanellus vanellus nests on lowland wet grassland in England and Wales: effects of nest density, habitat and predator abundance

There is concern that predation of Lapwing Vanellus vanellus nests may create additional pressure on declining populations of this species in Europe. At seven sites in England and Wales, daily nest predation rates on 1,390 nests were related to variables using Generalised Linear Mixed Models. The strongest predictor was Lapwing nest density (number of nests within 100 m): predation rates declined as nest density increased. Since nocturnal species, probably mammals, have been identified as the major predators of Lapwing nests at these sites, these results suggest that Lapwings are able to deter mammalian predators or may settle to nest at high densities in areas with low predation pressure. At the site level, there was no relationship between Lapwing nesting density and fox density, and a positive relationship with Carrion Crow Corvus corone nesting density. There was a weaker effect of distance to field boundary: nests closer to boundaries were more likely to be predated. Weak interactive effects between crow density and both nest visibility and distance to vantage point were identified in models using a reduced subset of nests. These were counter-intuitive, did not persist in the larger data set, and do not have obvious explanations. If Lapwings nesting at high density are able to deter predators, there are implications for land management. Smaller areas could be managed within potential breeding habitat to encourage Lapwings to nest in dense colonies. Selection of larger fields for such management, where nests could be located far from the field boundary should improve the value of such measures.     

Predator presence may benefit: kestrels protect curlew nests against nest predators

We studied whether the presence of breeding kestrels (Falco tinnunculus) affected nest predation and breeding habitat selection of curlews (Numenius arquata) on an open flat farmland area in western Finland. We searched for nests of curlews from an area of 6 km² during 1985–1993. For each nest found, we recorded the fate of the nest, and the distance to the nearest kestrel nest and to the nearest perch. We measured the impact of breeding kestrels on nest predation by constructing artificial curlew nests in the vicinity of ten kestrel nests in 1993. Curlew nests were closer to kestrel nests than expected from random distribution, eventhough kestrels fed on average 5.5% of curlew chick production. Predation risk by kestrels was lower than predation risk by corvids and other generalist predators, which predated 9% of curlew nests surviving farming practices and an unknown proportion of chicks. Artificial nest experiment showed that nest predation was lower close to kestrel nests than further away suggesting that the breeding association of curlews and kestrels was a behavioural adaptation against nest predation. Thus, the presence of a predator may sometimes be beneficial to prey, and prey animals have behavioural adaptations to these situations.     

Common Cuckoos Cuculus canorus change their nest‐searching strategy according to the number of available host nests

In recent decades, numerous studies have examined factors affecting risk of host nest parasitism in well‐known avian host–parasite systems; however, little attention has been paid to the role of host nest availability. In accordance with other studies, we found that nest visibility, reed density and timing of breeding predicted brood parasitism of Great Reed Warblers Acrocephalus arundinaceus by the Common Cuckoo Cuculus canorus. More interestingly, hosts had a greater chance of escaping brood parasitism if nesting was synchronized. Cuckoo nest searching was governed primarily by nest visibility at high host‐nest density. However, even well‐concealed nests were likely to be parasitized during periods when just a few hosts were laying eggs, suggesting that Cuckoos adjust their nest‐searching strategy in relation to the availability of host nests. Our results demonstrate that host vulnerability to brood parasitism varies temporally and that Cuckoo females are able to optimize their nest‐searching strategy. Moreover, our study indicated that Cuckoos always manage to find at least some nests to parasitize. Thus, in this case, the co‐evolutionary arms race should take place mainly in the form of parasitic egg rejection rather than via frontline pre‐parasitism defence.     

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.     

Nest predation in Reed Buntings Emberiza schoeniclus: an experimental study

Predation is a major cause of nest failure in many bird species. High levels of nest loss may be a consequence of habitat fragmentation, leading to increased amounts of edge habitat. Yet the evidence for generally high nest predation rates along edges in fragmented landscapes is ambiguous. Using real nests of Reed Buntings Emberiza schoeniclus in which artificial Reed Bunting and real Japanese Quail Coturnix japonica eggs were placed, we experimentally tested for edge effects on nest predation in highly fragmented reed Phragmites sp. habitats in the Swiss lowlands. We also examined seasonal patterns of predation and the impacts of nest visits by observers. We found evidence for an edge effect at the water-sided reed edge, with nests located closer to the water being more likely to be predated than those further away. Predation probability increased from early to late season, suggesting that nest predation may be density dependent. Probability of nest predation was only weakly influenced by whether or not a nest was visited. Our results suggest that the intensive reed management currently applied in Swiss nature reserves may result in unnaturally high levels of nest losses in the Reed Bunting, because reed bands are not wide enough to allow nest placement at a safe distance from reed edges.     

Poor reproductive success of Gray Vireos in a declining California population

Since the 1940s, populations of Gray Vireos (Vireo vicinior) in California have collapsed, presumably because of parasitism by Brown‐headed Cowbirds (Molothrus ater). In 2012 and 2013, we studied the vireo's nesting ecology to assess factors affecting two of California's largest remaining populations in the chaparral of San Diego County. Nest success was extremely low, with a model‐averaged probability of nest survival of only 0.08 (N = 95). More nest failures were due to predation (83%) than to cowbird parasitism (13%). Video‐recording at 30 nests revealed that California Scrub‐Jays (Aphelocoma californica) were the most common nest predator (67%). Of eight variables tested, height of shrubs surrounding the nest had the strongest negative influence on nest survival, but was more strongly correlated with cowbird parasitism than with jay predation. Despite frequent renesting, seasonal productivity was well below the level required to sustain a population, especially in northern San Diego County where we found no Gray Vireos at six of seven sites where they had been present from 1997 to 2001 and where cowbird parasitism was more frequent. The vireo's continuing range collapse contrasts with recent climate‐change models predicting a range expansion, highlighting the importance of demographic studies. Low nest success is likely contributing to population declines in California, and the additive effect of cowbird parasitism suppresses productivity. Conservation of Gray Vireos in California will likely require development of alternative approaches to cowbird and scrub‐jay control appropriate to sites widely scattered in rugged chaparral.     

Nest taphonomy of common terns (Sterna hirundo) on Poplar Island,Chesapeake Bay,Maryland

Mesozoic non-avian theropod dinosaurs displayed a diverse range of egg types and clutch forms, suggesting a variety of nesting behaviours, some of which may be shared with birds. More accurate inferences of these behaviours require taphonomic studies of modern nesting sites. Here, we document common tern (Sterna hirundo) nesting sites on Poplar Island in Chesapeake Bay, Maryland. Nests were surveyed on multiple occasions, documenting nest composition, density and distribution, as well as eggshell concentration and orientation. Three colonies yielded 79 tern nests with 193 eggs. Twelve nests hatched, 7 were predated, 30 failed and the fates of 30 remain unknown. Abundant eggshells occurred at the centre of the nests. Concave-up eggshell in or on the nest surface characterised hatched and predated nests, whereas eggshell forced into the subsurface seemed to favour concave-down orientation and may reflect post-hatching extended use of the nest. Eggs buried deep within the nest materials and/or substrate suggest adult abandonment. Quantitative data on eggshell orientation and observations regarding controls on nest distribution, egg predation and incorporation of intact eggs into the substrate at modern nesting sites provide physical guidelines for the improved interpretation of fossil nesting localities.     

Effects of parents and Brown‐headed Cowbirds (Molothrus ater) on nest predation risk for a songbird

Nest predation limits avian fitness, so ornithologists study nest predation, but they often only document patterns of predation rates without substantively investigating underlying mechanisms. Parental behavior and predator ecology are two fundamental drivers of predation rates and patterns, but the role of parents is less certain, particularly for songbirds. Previous work reproduced microhabitat‐predation patterns experienced by Yellow Warblers (Setophaga petechia) in the Mono Lake basin at experimental nests without parents, suggesting that these patterns were driven by predator ecology rather than predator interactions with parents. In this study, we further explored effects of post‐initiation parental behavior (nest defense and attendance) on predation risk by comparing natural versus experimental patterns related to territory density, seasonal timing of nest initiation, and nest age. Rates of parasitism by Brown‐headed Cowbirds (Molothrus ater) were high in this system (49% nests parasitized), so we also examined parasitism‐predation relationships. Natural nest predation rates (NPR) correlated negatively with breeding territory density and nonlinearly (U‐shaped relationship) with nest‐initiation timing, but experimental nests recorded no such patterns. After adjusting natural‐nest data to control for these differences from experimental nests other than the presence of parents (e.g., defining nest failure similarly and excluding nestling‐period data), we obtained similar results. Thus, parents were necessary to produce observed patterns. Lower natural NPR compared with experimental NPR suggested that parents reduced predation rates via nest defense, so this parental behavior or its consequences were likely correlated with density or seasonal timing. In contrast, daily predation rates decreased with nest age for both nest types, indicating this pattern did not involve parents. Parasitized nests suffered higher rates of partial predation but lower rates of complete predation, suggesting direct predation by cowbirds. Explicit behavioral research on parents, predators (including cowbirds), and their interactions would further illuminate mechanisms underlying the density, seasonal, and nest age patterns we observed.     

Brood parasitism by cowbirds: risks and effects on reproductive success and survival in indigo buntings

We observed brood parasitism by brown-beaded cowbirds (Molothrusater) on indigo buntings (Passerina cyanea) and estimated dieimpact of parasitism on the success of the individual buntingsin their current nests and in their future survival and reproduction.Rates of parasitism over 8 years were 26.6% in 1040 nests and19.8% in 693 nests in two areas in southern Michigan. Risk ofparasitism was high early in the season; half the bunting nestswere begun after the end of the cowbird season. Risk was independentof female age, plant containing the nest, or habitat The immediatecost of parasitism was 1.19 and 1.26 fewer buntings fledgedper nest. Bunting success was lower in parasitized nests withcowbird eggs (nests were more likely to be deserted or predated),lower when the cowbird nestling failed (nests were more likelyto be predated), and lower when the cowbird fledged (fewer buntingsfledged) compared to nonparasitized nests. Costs were due toremoval of a bunting egg when die cowbird laid its own egg andto competition for parental care of the cowbird and buntingnestlings. Buntings that fledged from nests where a cowbirdalso fledged were only 18% as likely to survive and return totheir natal area in the next year as buntings from nests wherea cowbird did not fledge. Long-term effects of cowbird parasitismon adult breeding later in the season, survival to the nextseason, and reproductive success in the next season were negligiblewhen compared between birds that reared a cowbird and birdsthat reared only a bunting brood, or between birds that wereparasitized and birds that escaped parasitism. The results indicatelittle long-term cost of brood parasitism on individual fitnessof adult buntings beyond the impact on the current nest andthe survival of buntings that fledge from it; nearly all costis to the parasitized brood.     

Habitat and Landscape Effects on Brood Parasitism,Nest Survival,and Fledgling Production in Swainson's Warblers

ABSTRACT Numerous factors, including nest predation and brood parasitism, may limit populations of neotropical migratory birds. However, nest predation and brood parasitism are not constant, and temporal, biological, habitat, and landscape factors can affect the likelihood of these events. Understanding these patterns is important for species of conservation concern for which managers seek to provide quality habitat. One such species, the Swainson's warbler (Limnothlypis swainsonii), is a neotropical migrant that breeds primarily in bottomland hardwood forests of the southeastern United States. Little is known of factors influencing reproductive success of this rare, yet locally abundant, species. From 2004 through 2007, we examined factors influencing reproductive success of Swainson's warblers at 2 sites in eastern Arkansas, USA, St. Francis National Forest and White River National Wildlife Refuge. We used 2-stage modeling to assess the relationship between 1) temporal and biological, and 2) habitat and landscape factors and brood parasitism, nest survival, and fledgling production. Brood parasitism was greater in this population (36%) than reported elsewhere (≤ 10%), but decreased throughout the breeding season. Nest survival was comparable to or lower than in other populations of this species and increased throughout the breeding season. The probability of brood parasitism was greater near forest edges. Although nests of Swainson's warblers were often associated with giant cane (Arundinaria gigantea), nest survival had a weak negative association with cane density. For nests that were successful, the best predictor of number of Swainson's warblers fledged was brood-parasitism status: nonparasitized nests fledged 2.75 young, whereas parasitized nests fledged 0.60 Swainson's warblers. Our findings suggest that managing and restoring relatively high-elevation bottomland forests that are located far from agricultural edges should increase Swainson's warbler productivity.     

Nestbox provisioning in a rural population of Eurasian Kestrels: breeding performance,nest predation and parasitism

The breeding biology of the Eurasian Kestrel Falco tinnunculusin nestboxes in farmland was studied to test for differences between artificial and natural sites. We report on the direct effect of nestbox provisioning on some life-history traits and how nestbox use affects nest predation and parasitism. Five types of nest-sites were available: nestboxes on poles and trees (artificial sites), stick nests on trees, stick nests on pylons and holes in buildings (‘natural’ sites). The Kestrel population increased from 23 pairs in 1993 (prior to nestbox installation) to 55 in 1998 as nestboxes were provided. In general, pairs breeding in trees started to lay later than those nesting in nestboxes on poles or in building holes, but this difference was probably associated with habitat quality rather than nest type. Differences in clutch size were found between nest-sites in some years, and were associated with laying date and, probably, with variation in territory quality. Using only data from successful nests, pairs breeding in nestboxes produce more fledglings than those in building holes or pylons. The frequency of nest predation was higher in natural sites than in nestboxes. The number of fledglings from pairs breeding in nestboxes was higher than from those breeding in old stick nests in trees when all nests were considered. Nestbox provisioning had no effect on the occurrence of the ectoparasite Carnus hemapterus, but chicks from nestboxes showed higher intensity of infection. Our results suggest that nestbox provisioning increases reproductive success and the frequency of nest predation or intensity of parasite infestation in Kestrels.     

Conspecific nest parasitism is associated with inequality in nest predation risk in the common goldeneye (Bucephala clangula)

Previous studies of the role of nest predation in conspecificnest parasitism have not taken into account the possibilitythat predation risk may not be randomly distributed among nestsites and that breeding individuals may use different cues toassess the risk and adjust their reproductive tactic betweenyears accordingly. Especially in cavity-nesting species, therole of nest predation in conspecific nest parasitism has beendownplayed, while the role of nest site limitation has beenhighlighted. Using both observational and experimental data,I show that in the common goldeneye (Bucephala clangula), acavity-nesting species in which conspecific nest parasitism iscommon, predation risk varies considerably between nest sitesand does not follow a random expectation. The inequality inpredation risk between nest sites also showed up in the occurrenceof parasitized nests in an experimental setup. Nests parasitizedin year t were more frequent in those nest sites that were notdepredated during the previous nesting attempt in year t - nthan in nest sites that were depredated and in control nestsites that had not been used for nesting before. A nest siteaddition experiment revealed that conspecific nest parasitismwas not associated with nest site limitation. My findings givesupport for the hypothesis that nest predation is an importantecological factor explaining conspecific nest parasitism ingoldeneyes.     

Breeding ecology of the Eastern Great Reed Warbler Acrocephalus arundinaceus orientalis at Lake Kasumigaura,central Japan

CapsuleTwo populations of the Eastern Great Reed Warblers, one close to settlements and one far away, differed mainly in nest losses which were higher at the latter site.

Aims To compare the breeding ecology of two Japanese populations, and with breeding data from Polish sites.

Methods We studied two sites in 1996. The Seimei site comprises a natural reed-bed (Phragmites australis) (2.0 ha) c. 2 km from residential areas. The Sakura site occurs as smaller reed-bed (0.8 ha) close to residential areas. Field study comprised mainly nest searching and nest monitoring.

Results Breeding density, nest height, number of stems supporting nest, clutch size and brood size were not significantly different between sites. The proportion of nests built on reed stems standing in the water (60%) was significantly higher at the Seimei site (P < 0.001), and the warblers in this habitat experienced significantly higher nesting failure (P < 0.05). Predation was a principal cause of failure at both sites. Significantly more nests suffered from predation at Seimei (53%) than at Sakura (16%). Breeding density was higher at both sites compared with European populations but it fell within ranges of other Japanese populations. Mean first-egg date of first brood does not differ between our sites and Polish ones.

Conclusion The differences between the two Japanese populations and between Japanese and Polish populations were relatively small and were seen mainly in nest losses, breeding density and proportion of nests built over water.     

Diel timing of nest predation changes across breeding season in a subtropical shorebird

Predation is the most common cause of nest failure in birds. While nest predation is relatively well studied in general, our knowledge is unevenly distributed across the globe and taxa, with, for example, limited information on shorebirds breeding in subtropics. Importantly, we know fairly little about the timing of predation within a day. Here, we followed 444 nests of the red‐wattled lapwing (Vanellus indicus), a ground‐nesting shorebird, for a sum of 7,828 days to estimate a nest predation rate, and continuously monitored 230 of these nests for a sum of 2,779 days to reveal how the timing of predation changes over the day and season in a subtropical desert. We found that 312 nests (70%) hatched, 76 nests (17%) were predated, 23 (5%) failed for other reasons, and 33 (7%) had an unknown fate. Daily predation rate was 0.95% (95%CrI: 0.76% – 1.19%), which for a 30‐day long incubation period translates into ~25% (20% – 30%) chance of nest being predated. Such a predation rate is low compared to most other avian species. Predation events (N = 25) were evenly distributed across day and night, with a tendency for increased predation around sunrise, and evenly distributed also across the season, although night predation was more common later in the season, perhaps because predators reduce their activity during daylight to avoid extreme heat. Indeed, nests were never predated when midday ground temperatures exceeded 45℃. Whether the diel activity pattern of resident predators undeniably changes across the breeding season and whether the described predation patterns hold for other populations, species, and geographical regions await future investigations.     

Nest-site selection and predation in Savi's Warblers Locustella luscinioides

Capsule Savi's Warblers preferred sites dominated by high and dense Juncus and Rubus with thick litter, and avoided pure reeds; predation was higher in sites with less litter.

Aim To describe nest-site selection and identify which habitat and nest features influence predation risk.

Methods Comparisons were made between habitat characteristics measured at nest-sites and random points, and between predated and successful nests.

Results Total vegetation cover, litter thickness, habitat type, undergrowth height and undergrowth cover, which were higher or denser at nest-sites, were the most important variables influencing the distribution of Savi's Warbler nests. Nests were most often predated in sites with low litter thickness.

Conclusion Savi's Warblers are dependent on the presence of dense low vegetation and litter for nesting, which should be maintained close to or within reed-beds for their benefit.     

Different nest predator guild associated with egg size in the Patagonian temperate forest

Capsule: Studies of nest predation using artificial nests need to consider the effect of egg size on the types of predator that are detected.

Aims: To estimate the nest predation rate in the Patagonian temperate forest and evaluate the influence of egg size on predator guild.

Methods: On different plant species, we placed 108 nests each containing eggs of either Atlantic Canary Serinus canaria or Common Quail Coturnix coturnix, and a model clay egg of equal size to the real egg. Nest predators were identified from the marks left on the clay eggs or by videos recorded using camera traps.

Results: 86% of the nests were predated. Birds, mainly Chimango Caracara Milvago chimango, were the main nest predators. A marsupial, the Monito del Monte Dromiciops gliroides, and rodents also contributed to nest predation. Nest predation rates were similar for both egg sizes but the nest predator guild was different. Birds and rodents preyed on both eggs but the Monito del Monte consumed mainly small eggs.

Conclusion: Egg size did not influence the rate of nest predation but, instead, affected the nest predator guild. Consequently, in order to avoid underestimating the impacts of small predators, egg size should be considered in studies of nest predation.     

Experiments with artificial nests on predation in reed habitats

We performed nest predation experiments with artificial nests in reedbeds investigating whether nest predation pressure is different at the water-reed edge and the grassland-reed edge compared with the reed interior. Furthermore, we tested the effects of vegetation structure (reed density, height and thickness) and the effect of other nest site characteristics (distance from edge, water depth) on the success of artificial nests. The experiments were completed 3 times during the breeding season in 2001 at Lake Neusiedl, Austria. Each artificial nest resembled Great Reed Warbler (Acrocephalus arundinaceus) nests and contained one plasticine and one Quail (Coturnix coturnix) egg and the predators were identified by marks left on the eggs. The potential predators were birds, probably the Marsh Harrier (Circus aeruginosus), gulls (Larus spp.) and reed warblers (Acrocephalus spp.). Nest survival data were analysed using the Mayfield method, and we performed a discriminant analysis for the data of vegetation and nest site characteristics. The nest predation was higher at the edges than in the reed interior, and was most pronounced in April, before the new reed sprouted. The reason for this finding was probably that after May the new reed contributed to greater concealment of the nests through the higher reed density and height.