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.     

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.     

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.     

Birds adopting weaver nests for breeding in Africa

Weavers build domed, long-lasting nests that may also be adopted by other species for breeding, probably reducing the energetic costs of nest building to varying degrees. In an extensive literature search, 57 species were found to have at least one record of adopting a weaver nest. There is one known obligate nest user, the Pygmy Falcon Polihierax semitorquatus. Four species were classed as near obligate nest adopters. Four species were listed as common, 10 as occasional, and 38 species as rare nest adopters. Other than the falcon and lovebirds Agapornis species, these nest adopters are passerines. Of the 57 species of nest adopters, 35 species had confirmed eggs and/or chicks found in the weaver nests. Most nest adopter species were in the Estrildidae family (20 species), with three estrildids classed as near obligates. This was followed by the Muscicapidae family, species that build cup nests. By building their cup nests inside weaver nests, there is likely protection from adverse weather and predators. Overall, there appeared to be a large diversity of nest adopter species for the traditional savanna living weavers (Ploceus, Bubalornis, Anaplectes, Plocepasser and Philetairus).     

Nest desertion by Grey Fantails during nest building in response to perceived predation risk

ABSTRACT Grey Fantails (Rhipidura albiscapa), a common Australian flycatcher, commonly desert their nests before egg‐laying. We tested the hypothesis that Grey Fantails desert incomplete nests in response to the attention of predators by placing a mounted Pied Currawong (Strepera graculina), a common nest predator, near fantail nests that were under construction. As a control, we placed a mounted King Parrot (Alisteris scapularis), a nonpredatory bird similar in size to Pied Currawongs, near other fantail nests. Four of six female fantails (67%) deserted incomplete nests in response to the presentation of the Pied Currawong. In contrast, none of the seven females presented with a mounted King Parrot deserted. Female Grey Fantails may use the attention of a predator at the nest during the building stage as a cue to desert. Such desertion may be adaptive for Grey Fantails because currawongs are large predators, making successful nest defense unlikely, and they also present considerable risk to adults. In addition, fantails may raise multiple broods during a breeding season and, therefore, have a high renesting potential.     

A shocking result—Electric fences protect western saw-shelled turtle (Myuchelys bellii) nests from depredation by foxes

Introduced red foxes (Vulpes vulpes) are a major predator of freshwater turtle nests in Australia. We evaluated the effectiveness of electric fences, in combination with individual nest protection, for shielding western saw-shelled turtle (Myuchelys bellii: Chelidae) nests from predation by foxes. We compared the numbers of raided and intact turtle nests found in paired fenced treatment and unfenced control areas of streambank. We also individually protected all intact nests found in both area types with wire mesh or a steel cage. The total numbers of nests found in treatment and control areas did not significantly differ from parity, but significantly more intact nests were found in treatment areas and significantly more raided nests in control areas. The fences were occasionally damaged by livestock, wildlife and flooding, rendering them inoperative for varying periods of time until repair. However, foxes raided nests inside the fences on only two occasions, despite these breaks in functionality. Our study demonstrates that electric fences can provide an effective method of protecting entire nesting areas from depredation by foxes.     

The different roles of the roof density and nest size in the Iberian magpie nest

Nest volume in magpies is modulated by sexual selection. However, density of material that compounds the nest could also affect sexual signalling, and we may expect that high-quality pairs build larger and denser nests, with these two variables being positively correlated. As found for nest volume, density of nest thatching should be negatively related with laying date, which is indicative of pair quality. Alternatively, these traits could be subjected to different selective pressures and, hence, indicate different qualities. Results of the present study on a population of magpies in the Iberian Peninsula showed no relationship between nest volume and roof density. However, roof density was positively correlated to laying date, so that those nests that are built at later dates tend to have denser roof material. These data support the theory that density of roof material is related to nest predation, as there is a greater risk of predation at the end of the breeding season. Thus, nest volume and roof density could be two independent elements of a magpie’s nest, which have different ecological roles, as they would be subjected to different selection pressures. I suggest that nest size is a predictor of parental quality as has been previously demonstrated, while roof structure (roof density) is related to predation risk.     

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.     

Individual variation in nest size and nest site features of the Bornean orangutans (Pongo pygmaeus)

Nest construction is a daily habit of independent orangutans for sleeping or resting. Data on their nests have been used in various ecological studies (e.g., density estimation, ranging behavior, evolution of material culture) because they are the most observable field signs. We investigated nest size and nest site features of Bornean orangutans in the wild during 10 months' fieldwork at three sites in East Kalimantan, Indonesia: Kutai National Park, Birawa, and Meratus. To examine individual variation, we followed 31 individual orangutans and recorded the 92 nests they made for nest size (diameter) and nest site features (height of nest above ground, tree species used for the nest site, the diameter and height of the tree, whether the nest was new or reused, and nest location within the tree). Analyses taking age–sex classes of the focal individuals into consideration showed significant age–sex differences in nest size and location, but not in nest height or nest tree features (diameter, height of tree, and height of lowest branch). Mature orangutans (adult females, unflanged and flanged males) made larger nests than immatures (juveniles and adolescents). Flanged male orangutans with larger nests used stable locations for nesting sites and reused old nests more frequently than immatures. The overall proportion of nests in open (exposed) locations was higher than in closed (sheltered) locations. Flanged males and immatures frequently made open nests, whereas adult females with an infant preferred closed locations. The good correspondence between nest size and age–sex classes indicates that nest size variation may reflect body size and therefore age–sex variation in the population. Am. J. Primatol. 71:393–399, 2009. © 2009 Wiley‐Liss, Inc.     

Nesting biology of Asian paper wasps Polistes chinensis antennalis Pérez,and Australian paper wasps P. humilis (Fab.) (Hymenoptera: Vespidae) in northern New Zealand

Abstract

We recorded the numbers of cells, and where possible distinguished between cells containing pupating larvae and vacated cells, from 585 paper wasp nests from the northern North Island, New Zealand, plus nest site characteristics of 540 of these nests. Nests of Polistes chinensis antennalis and P. humilis developed at similar rates in early summer. P. c. antennalis nests were larger at the Post‐emergence stage than those of P. humilis, and contained more vacated cells but less capped cells. All of the P. c. antennalis nests had reached the Post‐emergence stage by February in Northland, but not in the other regions. P. c. antennalis nests in the Post‐emergence stage were larger in Northland than further south, and contained the most capped or vacated cells. Nests of both species were usually found in northern‐facing sites. Substrate did not affect nest size. Differences between the species in nest sites included greater use of manmade structures by P. c. antennalis; the use of leaves by P. humilis only; and a higher average nest site height in P. humilis. These differences in nest site selection may reduce competition between the species.     

Excavation and architecture of Argentine ant nests

We used x-ray computed tomography to study the elaboration of nest structures in small sand-filled nest boxes by Argentine ant (Linepithema humile) colonies composed of 10, 100, and 1000 workers. The pattern of nest growth was consistent with a process of density-dependent stimulation of excavation, which subsided as nests grew and the density of digging stimuli declined. Thus, nest excavation would be auto-regulating, and final nest size should be adjusted to colony size. We found that excavation rates and final nest sizes increased with colony size, but were not tenfold greater in 1000-worker colonies than in 100-worker colonies. In the largest colonies, the internal surface area scaled allometrically with volume, so that more surface was obtained relative to volume excavated as the nest grew. Although the gross features of Argentine ant nests, such as total size, seem explicable by a simple, self-organized regulatory process, other features of the nest architecture will require further investigation. Received 3 March 2005; revised 26 April 2005; accepted 3 May 2005.     

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.     

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.     

Construction of Nest Defensive Structure According to Offspring Value and Its Effect on Predator's Attack Decision in Paper Wasps

Various organisms are known to build nests with defensive structures to protect their offspring from predation, but our understanding of plasticity in the nest structure remains poor. In this study, we investigated whether a paper wasp, Polistes chinensis antennalis, adjusted the construction of nest defensive structure according to the value of their offspring, and we also analysed the effect of adjusting the construction of the structure on predator's decision to attack. P. chinensis antennalis foundresses start a colony and maintain her nest alone until the emergence of workers. During this stage, foundresses often construct a defensive structure on cocoon caps of pupae using nest materials (pulp), which prevents predation of pupae by conspecifics from other nests. The value of pupae to the foundress varies among those in a nest, where the value is higher in pupae that spun the cocoon (and initiated pupation) earlier than other pupae in the nest. From field observations, we found that foundresses constructed a larger pulp structure on the cocoons of pupae that cocooned earlier in the order of cocoon spinning, even after considering confounding factors. We also found that the probability of a pupa being attacked by conspecific intruders decreased with the size of pulp structure on the cocoon. This indicates that intruders avoid attacking cocoons with larger pulp structures. Our study indicates that foundresses adjust the construction of nest defensive structures according to their offspring value, and this allows them to protect the high‐value offspring efficiently and effectively.     

Experimental Study of Nest-site Selection in the Biscutate Swift (Streptoprocne biscutata, Aves: Apodidae) in Southern Brazil

Biscutate swift Streptoprocne biscutata nests are usually built on protected rocky cliff walls. Birds often renest at the same location. Remains of previous nests may offer information about potential nests and quality of nest-sites. Here, we experimentally study nest-site selection to test the hypothesis that information from previous nests is used in current nest-site selection. We placed old nest material at artificial nest-sites to test whether new nest-sites are chosen based on the presence of nesting material. We also tested whether the use of natural nest-sites is influenced by nesting material by creating two types of natural sites: previously used natural nest-sites with vestiges of old nests removed and never used natural nest-sites to which vestiges of old nests were added. In the first experiment, in 139 nest-use opportunities, 16 artificial nest-sites were used, all of which included vestiges. In the second experiment, in 91 nest-use opportunities, four nests were in previously unused but natural locations to which vestiges had been added, 22 nests were in previously used sites without vestiges, and the remaining 65 nests remained unused. Two processes are apparently in action: first, prior experience and memory; second, vestiges indicate where nesting has occurred, possibly useful for first breeding, or for imperfect memory. Previous nesting information may explain why swifts use nesting locations for many years and why new nesting colonies seldom form. This transmission of information suggests that swifts tend to be conservative and nest where previous nesting has occurred.     

Location matters: survival of artificial nests is higher in small grassland patches and near the patch edge

Nest survival is an important part of breeding success in grassland ecosystems, and the location of nests can determine vulnerability to different predators. We conducted an experiment with artificial nests to evaluate jointly the predation rate on nests at different spatial scales (landscape, patch and tussock) and the relative abundance of potential nest predators (small mammals and birds) in a temperate grassland area. In November 2014 and 2016, we installed 288 artificial nests in Common Pampas Grass Cortaderia selloana grasslands in the southeastern Pampas region, Argentina. The nests were placed in two 10-ha plots in a continuous grassland patch (c. 900 ha) within a reserve and in two small grassland patches (1.5 and 1.8 ha) in an agricultural matrix (landscape-scale), at the patch edge and inside the patches (patch-scale), and at two heights within the tussock grass (tussock-scale). In 2016, we also conducted live trapping of small mammals and surveyed birds along strip transects at the sampling sites. Nests located in patches within an agricultural matrix and near the edge had greater relative survival than those set in the reserve and inside the patches, respectively. This might be explained by the lower relative abundance of small mammals that we found outside the reserve. Artificial nest survival values recorded at the landscape-scale contrasted with those previously observed for natural nests. Our results could be partly explained by differences in nest density between agro-patches and those within the reserve. Future studies could also evaluate the role of parental nest defence on nest survival.     

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.     

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.     

Evidence of selection for egg crypsis in conspicuous nests

ABSTRACT The value of egg coloration as crypsis, once accepted as a general principle, has recently been questioned because most experiments have failed to show that egg coloration deters predation. The nest‐crypsis hypothesis postulates that, among species that build conspicuous nests, selection for egg crypsis is relaxed or absent because visually searching predators detect nests prior to eggs. I tested the nest‐crypsis hypothesis using the large, relatively conspicuous nests of American Robins (Turdus migratorius), and eggs that differed markedly in color that were collected from the nests of Red‐winged Blackbirds (Agelaius phoeniceus), Brewer's Blackbirds (Euphagus cyanocephalus), and Yellow‐headed Blackbirds (Xanthocephalus xanthocephalus). Each nest (N= 22) received a clutch of each species during three sequential predation trials that were 16 d in duration. The order of clutch presentation was randomized for each nest. Survival trends for Brewer's and Yellow‐headed Blackbirds were similar, and higher than those for clutches of Red‐winged Blackbirds. By the end of trials, overall survival of the three clutch types was roughly equivalent. However, clutches of Red‐winged Blackbird eggs, the most conspicuous egg type to the human eye, were discovered sooner by predators. Because the experimental design controlled for effects of nest crypsis, nest location, and nest size, this difference in egg survival can be attributed to differences in egg pigmentation. Thus, my results support a role for egg coloration as camouflage in conspicuous nests.