Monitoring Texas Wood Ducks With a Cooperative Nest-Box Program

ABSTRACT We analyzed 8 years of data from the Texas Cooperative Nest Box Program initiated in 1988 by Texas Parks and Wildlife, USA, as a means of involving private cooperators in statewide wood duck (Aix sponsa) management. Cooperators operated ≤9 boxes and most reported nest-box data for only 1 year (56.5%) and 2 years (20.6%) over the 8-year life of the project. Mean nest-box use differed among ecological regions of the state (F=4.23, df=6, P= 0.001) but did not exceed 30% in any region. Mean nest-box success ranged between 74–91% across ecological regions during 1988–1995, but annual estimates of nest-box success lacked precision (CVs >30%) in most years for all regions. Our project was unsuccessful as a management tool for monitoring wood duck demographics. Future efforts should focus on improving the amount and quality of data collected from box-nesting wood ducks.     

Experimental evidence for edge-related predation in a fragmented agricultural landscape

Abstract This study tested the hypothesis that increased predation of experimental nests occurs close to a forest edge in a fragmented agricultural landscape. Artificial nests and eggs of willie wagtails Rhipidura leucophrys and superb fairy-wrens Malurus cyaneus were used in experiments to assess the extent and nature of predation occurring throughout the known breeding seasons of these species. Predators were identified by the imprints they left in plasticine eggs, and by remote photography. Surveys of avian predators were undertaken to investigate the relationship between predation intensity and predator distribution and abundance. Avian predators accounted for almost all predation for which a predator could be identified (96%). Five of seven predator species photographed attacking wagtail nests were corvids or artamids. Fairy-wren nests suffered relatively low rates of predation (29%) compared to wagtail nests (87%). Increased predation at the habitat edge was recorded for wagtail nests only; predation was correlated with the distribution and abundance of predatory avian species. The different extent and pattern of predation on fairy-wren nests could be explained by problems in detecting predation by mammals, and by possible failure of avian predators to locate the cryptic nests.     

Building multiple nests is associated with reduced breeding performance in a south temperate population of Grass Wrens Cistothorus platensis platensis

Grass Wrens Cistothorus platensis build two types of non-breeding nest structures: platforms and dummy nests. Platforms are rudimentary accumulations of grasses concealed between vegetation. Dummy and breeding nests are dome-shaped with a similar structural layer. We used a nest-removal experiment and observational data to evaluate several hypotheses regarding the adaptive significance of building multiple nests in a south temperate population of Grass Wrens. Building non-breeding nests was not a strategy of males to attract additional females, as most of these nests were built after pair formation and both sexes collaborated during building. Building non-breeding nests was not a post-pairing display as the presence of multiple nests did not increase female investment in the breeding attempt: clutch size and female provisioning to nestlings did not differ between experimental and control territories where no non-breeding nests were removed. Similarly, in non-manipulated territories, clutch size and female provisioning were not correlated with the number of non-breeding nests or with males’ nest-building effort. Contrary to this hypothesis, the number of non-breeding nests was associated with delayed clutch initiation and reduced hatching success. The presence of non-breeding nests did not reduce nest predation and brood parasitism, which did not differ between experimental and control territories. We did not detect differences in concealment between non-breeding and breeding nests, suggesting that non-breeding nests were not the result of abandonment before egg-laying to reduce subsequent nest predation. Dummy nests did not provide shelter; they were not used frequently for roosting over the breeding season and were not maintained during the non-breeding season. We suggest that building non-breeding nests may be an attempt by males to manipulate the decision of females to breed with a mate they might otherwise reject or to start reproduction earlier than optimal for the females.     

Changing patterns of nest predation and predator communities along a tropical elevation gradient

Tropical montane communities host the world's highest beta diversity of birds, a phenomenon usually attributed to community turnover caused by changes in biotic and abiotic factors along elevation gradients. Yet, empirical data on most biotic factors are lacking. Nest predation is thought to be especially important because it appears to be common and can change selective pressures underlying life history traits, which can alter competitive interactions. We monitored 2538 nests, 338 of which had known nest predators, to evaluate if nest predation changes along a tropical elevational gradient. We found that nest predation decreased with elevation, reflecting the loss of lowland predators that do not tolerate colder climates. We found different “super” nest predators at each elevation that accounted for a high percentage of events, suggesting that selection pressures exerted by nest predator communities may be less diffuse than has been hypothesized, at least for birds nesting in the understory.     

Testing hypotheses about the function of repeated nest abandonment as a life history strategy in a passerine bird

Nest structures are essential for successful reproduction in most bird species. Nest construction costs time and energy, and most bird species typically build one nest per breeding attempt. Some species, however, build more than one nest, and the reason for this behaviour is often unclear. In the Grey Fantail Rhipidura albiscapa, nest abandonment before egg‐laying is very common. Fantails will build up to seven nests within a breeding season, and pairs abandon up to 71% of their nests before egg‐laying. We describe multiple nest‐building behaviour in the Grey Fantail and test four hypotheses explaining nest abandonment in this species: cryptic depredation, destruction of nests during storm events, and two anti‐predatory responses (construction of decoy nests to confuse predators, and increasing concealment to ‘hide’ nests more effectively). We found support for only one hypothesis – that abandonment is related to nest concealment. Abandoned nests were significantly less concealed than nests that received eggs. Most abandoned nests were not completely built and none received eggs, thus ruling out cryptic predation. Nests were not more likely to be abandoned following storm events. The decoy nest hypothesis was refuted as abandoned nests were constructed at any point during the breeding season and some nests were dismantled and the material used to build the subsequent nest. Thus, Grey Fantails are flexible about nest‐site locations during the nest‐building phase and readily abandon nest locations if they are found to have deficient security.     

Predation of experimental nests is linked to local population dynamics in a fragmented bird population

Artificial nest experiments (ANEs) are widely used to obtain proxies of natural nest predation for testing a variety of hypotheses, from those dealing with variation in life-history strategies to those assessing the effects of habitat fragmentation on the persistence of bird populations. However, their applicability to real-world scenarios has been criticized owing to the many potential biases in comparing predation rates of artificial and natural nests. Here, we aimed to test the validity of estimates of ANEs using a novel approach. We related predation rates on artificial nests to population viability analyses in a songbird metapopulation as a way of predicting the real impact of predation events on the local populations studied. Predation intensity on artificial nests was negatively related to the species' annual population growth rate in small local populations, whereas the viability of large local populations did not seem to be influenced, even by high nest predation rates. The potential of extrapolation from ANEs to real-world scenarios is discussed, as these results suggest that artificial nest predation estimates may predict demographic processes in small structured populations.     

Nest predators of woodland open-nesting songbirds in central Europe

I used time-lapse videotaping to identify predators of open songbird nests in fragmented deciduous woodland (nine plots, 2–10 ha each) in the Czech Republic from 2002 to 2006. I documented 22 species of predators at 171 nests of 13 species (mainly Blackcap Sylvia atricapilla , Song Thrush Turdus philomelos , Common Blackbird Turdus merula , Yellowhammer Emberiza citrinella and Chaffinch Fringilla coelebs ). The main predators were Pine Marten Martes martes (37% of 178 predation events), Jay Garrulus glandarius (29%), Buzzard Buteo buteo (7%) and Great Spotted Woodpecker Dendrocopos major (7%); mammals accounted for 48% of total predation. At least 3% of nests were depredated by multiple predators. In spite of their local abundance, Hooded Crows Corvus cornix did not present a serious threat for shrub nesting songbirds (< 1% of total predation). No predation by mice was recorded, suggesting that their importance has been overestimated in artificial nest studies. The proportional species composition of predators depended on which species occupied the monitored nest and location (study plot), but not on the year or the time of season. Corvids and raptors accounted for a relatively larger percentage of total predation of small ('warblers') and large ('thrushes') prey species, respectively, whereas carnivores were important predators of all prey species. Active nests of thrushes were only rarely robbed by Jays (< 4% of 52 events), presumably due to parental nest defence. Predation by woodpeckers was spatially clumped, probably due to individual foraging specialization. Predation by the other major predators was documented on most/all study plots.     

Nesting Success in Crimson Finches: Chance or Choice?

In avian systems, nest predation is one of the most significant influences on reproductive success. Selection for mechanisms and behaviours to minimise predation rates should be favoured. To avoid predation, breeding birds can often deter predators through active nest defence or by modifying behaviours around the nest (e.g. reducing feeding rates and vocalisations). Birds might also benefit from concealing nests or placing them in inaccessible locations. The relative importance of these strategies (behaviour vs. site selection) can be difficult to disentangle and may differ according to life history. Tropical birds are thought to experience higher rates of predation than temperate birds and invest less energy in nest defence. We monitored a population of crimson finches (Neochmia phaeton), in the Australian tropics, over two breeding seasons. We found no relationship between adult nest defence behaviour (towards a model reptile predator) and the likelihood of nest success. However, nest success was strongly related to the visibility of the nest and the structure of the vegetation. We found no evidence that adult nest building decisions were influenced by predation risk; individuals that re‐nested after a predation event did not build their nest in a more concealed location. Therefore, predator avoidance, and hence nest success, appears to be largely due to chance rather than due to the behaviour of the birds or their choice of nesting sites. To escape high predation pressures, multiple nesting attempts both within and between seasons may be necessary to increase reproductive success. Alternatively, birds may be limited in their nest‐site options; that is, high‐quality individuals dominate quality nest sites.     

Nest survival in year‐round breeding tropical red‐capped larks Calandrella cinerea increases with higher nest abundance but decreases with higher invertebrate availability and rainfall

Nest survival is critical to breeding in birds and plays an important role in life‐history evolution and population dynamics. Studies evaluating the proximate factors involved in explaining nest survival and the resulting temporal patterns are biased in favor of temperate regions. Yet, such studies are especially pertinent to the tropics, where nest predation rates are typically high and environmental conditions often allow for year‐round breeding. To tease apart the effects of calendar month and year, population‐level breeding activity and environmental conditions, we studied nest survival over a 64‐month period in equatorial, year‐round breeding red‐capped larks Calandrella cinerea in Kenya. We show that daily nest survival rates varied with time, but not in a predictable seasonal fashion among months or consistently among years. We found negative influences of flying invertebrate biomass and rain on nest survival and higher survival of nests when nests were more abundant, which suggests that nest predation resulted from incidental predation. Although an increase in nest predation is often attributed to an increase in nest predators, we suggest that in our study, it may be caused by altered predator activity resulting from increased activity of the primary prey, invertebrates, rather than activity of the red‐capped larks. Our results emphasize the need to conduct more studies in Afro‐tropical regions because proximate mechanisms explaining nest predation can be different in the unpredictable and highly variable environments of the tropics compared with the relatively predictable seasonal changes found in temperate regions. Such studies will aid in better understanding of the environmental influences on life‐history variation and population dynamics in birds.     

Nests of the soil dwelling sweat bee Augochloropsis caerulans (Hymenoptera: Halictinae) in a waterlogged environment in southern Brazil

A swampy nest site of the sweat bee Augochloropsis caerulans (Vachal, 1903) in southern Brazil is reported. The bees colonized small earth mounds scattered throughout a water-covered area. Although the substrate of these mounds has high organic matter content, the risk of microbial infestation seems not to be enhanced owing to permanent water saturation. The nests are shallow and can be found 3 cm above the water table. Each nest consists of a cluster of vertically oriented cells on pillars in an oval shaped cavity. The specific nest architecture is thought to mitigate microbial infestation of the brood and to prevent water excess. Nests of A. caerulans are not restricted to water-saturated substrates, but the specific nest architecture presumably enables the bee to propagate in such habitats.     

Behavioural plasticity under a changing climate; how an experimental local climate affects the nest construction of the zebra finch Taeniopygia guttata

Successful reproduction in most avian species is dependent on the construction of a nest that provides protection and a suitable microclimate for the eggs and developing nestlings. Observational studies suggest that climatic variation may affect the structure of the nest, but to date there have been no attempts to experimentally determine the role that local climate plays in the construction of a suitable nest. Using a within‐individual counter balanced design we investigated how nest composition and construction differ in zebra finches breeding in ambient conditions of 18°C and 30°C. We found that at 18°C birds built nests that were over 20% heavier, and with significantly more thread and less grass than those built at 30°C. Our results highlight the degree of plasticity in nest building behaviour in relation to local ambient conditions. These results suggest that nest building behaviour is one route through which birds can respond to a changing climate and modify the microclimate of their nest in line with projected changes in ambient conditions.     

incR: a new R package to analyse incubation behaviour

Incubation represents a life stage of crucial importance for the optimal development of avian embryos. For most birds, incubation poses a trade‐off between investing in self‐maintenance and offspring care. Furthermore, incubation is affected by environmental temperatures and, therefore, will be likely impacted by climate change. Despite its relevance and readily available temperature logging methods, avian incubation research is hindered by recognised limitations in available software. In this paper, a new quantitative approach to analyse incubation behaviour is presented. This new approach is embedded in a free R package, incR. The flexibility of the R environment eases the analysis, validation and visualisation of incubation temperature data. The core algorithm in incR is validated here and it is shown that the method extracts accurate metrics of incubation behaviour (e.g. number and duration of incubation bouts). This paper also presents a suggested workflow along with detailed R code to aid the practical implementation of incR.     

Nest sites as limiting resources for cavity‐nesting birds in mature forest ecosystems: a review of the evidence

ABSTRACT Assumptions that populations of cavity‐nesting birds are limited by access to nest sites have largely been based on anecdotal reports or correlative data. Nest‐box‐addition experiments or tree‐cavity‐blocking experiments are potentially rigorous ways to investigate how densities of breeding birds are affected by access to nest cavities. Experimental evidence indicates that natural tree holes are limited in human‐altered landscapes, but the possibility that cavity nests are limited in old growth (unmanaged) forests is less clear. I reviewed 31 nest‐cavity‐removal or addition experiments conducted with 20 species of cavity‐nesting birds in mature forests. Of these 31 experiments conducted with a variety of different species of birds, only 19% reported statistically significant changes in breeding densities. However, none of these studies included data about the reproductive history of individuals colonizing the boxes (i.e., whether birds using the boxes would have otherwise been floaters or that birds excluded from blocked cavities on the plots did not simply move elsewhere), so they provided no strong evidence that the number of breeding pairs was limited by availability of nest sites at the population scale. Although some studies indicate that nest sites are limited at local (plot) scales in old growth forests, there is still little empirical evidence for nest‐site limitation at the population‐ and landscape‐level in mature, unmanaged forests. I review the challenges in designing and interpreting box‐addition experiments and highlight the main gaps in knowledge that should be targeted in the future.     

Nest site, laying period, and breeding success of the Woodchat Shrike (Lanius senator) in Mediterranean France

Summary Breeding habitats in Mediterranean France consist in open, dry grasslands with a low and discontinuous grass layer and scattered bushes and trees. The choice of nest supports was largely opportunistic, the most abundant suitable nest support type (bush or tree) and the most abundant species being present at each study site have been used. About 75% of the nests were placed at heights between 1 and 3 m. Laying period lasted from 9 May until 6 July (peak of first clutches: 21–30 May). Mean clutch size was 5.14±0.82 eggs (n=114). Breeding success was independent from the site, the height and the concealment of nests. Mean survival rate of nests from laying to fledgling was 0.365. The main cause of low breeding success was high nest predation exerted by a rich guild of predators. The species is mainly threatened through dramatic habitat shrinkage due to pastoralism reduction leading to closures of lightly bushed grasslands in Mediterranean France.

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Nistplatzwahl, Legeperiode und Bruterfolg des Rotkopfwürgers (Lanius senator) in Südfrankreich

Zusammenfassung Als Bruthabitat bevorzugt der Rotkopfwürgers im mediterranen Südfrankreich offene und trockene Graslandlandschaften mit niedrigem oder lückigem Grasbewuchs und einzelstehenden Büschen und/oder Bäumen. Häufigster Nestträger ist die jeweils im Brutterritorium häufigste Baum- oder Buschart. Ungefähr 75% der Nester standen zwischen 1 und 3 m über Boden. Die Legeperiode reichte vom 9. Mai bis 6. Juli (Gipfel der Erstgelege am 21.–30. Mai und der Ersatzgelege am 20.–24. Juni). Die Gelegegröße bestand aus 3 bis 7, meist 5 Eier (Erstgelege im Mittel 5,35±0,71 Eier, Ersatzgelege: 4,68±0,85). Der Bruterfolg war unabhängig von der Lage, der Höhe und der Verborgenheit des Nestes. Die mittlere Überlebensrate eines Nestes zwischen Bebrütung des Geleges und Ausfliegen der Jungen betrug 0,365. Dieser niedrige Bruterfolg wurde hauptsächlich durch Nesträuber verursacht. In Südfrankreich ist die Art aber vor allem durch die zunehmende Verschließung der Bruthabitate infolge des Rückgangs des extensiven Weidebetriebs gefährdet.

     

Spatial Nest‐Settlement Decisions in Digger Wasps: Conspecifics Matter more than Heterospecifics and Previous Experience

Research into the driving forces behind spatial arrangement of wasp nests has considered abiotic environmental factors, but seldom investigated attraction or repulsion towards conspecifics or heterospecifics. Solitary female digger wasps (Hymenoptera) often nest in dense aggregations, making these insects good models to study this topic. Here, we analysed the nesting patterns in an area shared by three species of the genus Bembix, in a novel study to discover whether female wasps are attracted to or repulsed by conspecific nests, heterospecific nests or their own previously established nests when choosing nest‐digging locations. Early in the season, each species showed a clumping pattern of nests, but later in the season, a random distribution of nests was more common, suggesting an early conspecific attraction. Such behaviour was confirmed by the fact that females started building their nests more frequently where other females of their species were simultaneously digging. The distances between subsequent nests dug by individual females were shorter than those obtained by random simulations. However, this pattern seemed to depend on the tendency to dig close to conspecifics rather than remain in the vicinity of previous nests, suggesting that females' experience matters to future decisions only on a large scale. Nesting patches within nest aggregations largely overlapped between species, but the nests of each species were generally not closer to heterospecific nests than expected by chance, suggesting that females are neither repulsed by, nor attracted to, congenerics within nest aggregations. A role of the spatial distribution of natural enemies on the observed nesting patterns seemed unlikely. Bembix digger wasp nest aggregations seem thus to be primarily the result of female–female attraction during nest‐settlement decisions, in accordance with the ‘copying’ mechanisms suggested for nesting vertebrates.     

Dummy birds in artificial nest studies: an experiment with Red-backed Shrike Lanius collurio

Capsule Dummy birds placed on artificial nests increase nest survival, and their use should be considered in future studies of nest predation.     

Comparative nest survival of three sympatric loon species breeding in the Arctic

Identifying factors influencing nest survival among sympatric species is important for understanding and managing sources of variation in population dynamics of individual species. Three species of loons nest sympatrically in northern Alaska and differ in body size, life history characteristics, and population trends. We tested the effects of competition, nest site selection, and water level variations on nest survival of Pacific Gavia pacifica, yellow‐billed G. adamsii, and red‐throated loons G. stellata on the Arctic Coastal Plain in Alaska. Although overall nest survival rates did not differ between species, the factors influencing nest survival varied. Nest site selection influenced nest survival for Pacific and yellow‐billed loons, with both species having high nest survival when nesting on islands and peninsulas, likely due to a reduction in access by terrestrial predators. However, on mainland shorelines, Pacific loons had lower nest survival than yellow‐billed loons, and used a higher proportion of vegetation mats for nest sites suggesting that their smaller body size makes them less adept at nest defense. Nest site selection did not influence nest survival of red‐throated loons corresponding to our result of no nest site preferences by this species. Initiation date had a strong influence on nest survival for Pacific and yellow‐billed loons with nests laid earlier having higher survival. Pacific and yellow‐billed loon nests were susceptible to flooding due to precipitation, which contrasted with red‐throated loons that nest on smaller lakes with lower water level variations. Competition did not affect nest survival for any of the species likely due to most territorial encounters occurring prior to incubation. The only influence we found on red‐throated loon nest survival was differences among years. Our results indicate that loons chose nest sites based on predation risk and that factors influencing breeding success of closely related species may differ under similar breeding conditions.     

The breeding biology of Grallaria and Grallaricula antpittas

ABSTRACT Grallaria and Grallaricula antpittas are poorly known ground antbirds (Formicariidae), which reach their center of diversity in the tropical Andes region. Here we review published literature on the reproductive ecology of these two genera, summarizing and synthesizing the information. Nests have been described for 13 of the 31 species of Grallaria and four of the eight species of Grallaricula. For both genera, nests are open cups placed either against a strong support (e.g., tree trunks; Grallaria) or with multiple small supports (e.g., vine tangles; both genera). Nest lining is generally sparse, with nest cup composition ranging from humid material (e.g., moss) to primarily sticks and leaf material, depending on the species. Grallaria typically lay two bluish‐green to turquoise eggs, sometimes with spotting, whereas Grallaricula lay 1–2 eggs with heavy markings and pale brown or buffy (rarely light green) background coloration. For the few species where information is available, both male and female parents are believed to participate in building, incubation, and nestling provisioning, with high incubation attentiveness (often >90%, especially later in incubation), and incubation periods of 17–21 d (Grallaria) and 15–20 d (Grallaricula). Grallaria nestlings are frequently fed earthworms (Oligochaeta) in addition to a variety of arthropods. Nestlings have pale skin (Grallaria) or dark skin (both genera), with pale or dark down (Grallaria) or red‐brown down (Grallaricula). Nestlings in both genera usually have brilliant orange mouth linings and cloacas, and usually fledge 15–19 d post hatching. Rapid probing, where adults rapidly thrust their bills into the nest and lining, is commonly observed across species during incubation and nestling periods, but its function remains unknown. Overall, our knowledge of the breeding biology of antpittas has improved significantly in recent years. However, much remains to be learned for most species.