Numerical Data on African Birds' Behaviour at the Nest.—II. Psalidoprocne liolomelsena massaica Neum., the Rough-wing Bank-Martin

Psalidoprocne holomelæna makes a pad of beard lichen ( Usnea ) on a ledge or in a narrow natural hole at any depth up to about 2 feet. The numerical data are derived from 800 hours' observations at Amani divided between seven nests. There is no proof that both members of a pair share brooding or feeding duty.
The incubation period is 19 days, the fledging 24–27.
The extent to which the eggs were incubated varied from 31 to 66 per cent., apparently without relation to temperature. The frequency curves of duration of spells on eggs, and of intervals when the eggs were uncovered, contrast strikingly with those of Hirundo smithii. In Psalidoprocne both spells and intervals are much longer, most of them being between 8 and 20 minutes. Absences exceeding 30 minutes are rare, but 84 minutes has been recorded.
For the first week after hatching the young are brooded as much as the eggs, but after that date the amount of brooding they get varies widely from nest to nest.
During the last half of the fledging period the normal brood of two young receives 12 to 20 visits, presumably with food, per 200 minutes (only one-fifth as many as a brood of two Hirundo smithii ). A solitary Psalidoprocne , nestling got 80 per cent, as much attention as a pair.
Nearly all the young leave the nest-hole within three hours of sunrise. They fly in the absence of their parents, and efficiently from the first moment.     

NESTING OF THE PURPLE-THROATED CARIB HUMMINGBIRD

We present data on certain parts of the nesting biology of the Purple-throated Carib Humming- bird Eulampis jugularis on the island of Dominica, British West Indies. We watched two nests with eggs and young and a single nest under construction. Incubation was in short periods averaging about six minutes. Females at both nests with eggs continued adding material to the nest until the end of incubation. We suggest that this common practice among hummingbirds may insure that a limited amount of energy at the time of initial nest-building and egg-production is optimally apportioned between the two activities. Brooding ceased in one nest when the young were about 13 days old. Feeding rates stayed relatively constant at one to two per hour throughout the nearly complete nestling period in one nest. Average time per feeding declined, apparently as the female-young interaction became more efficient with maturation of the young. Nesting females foraged on both insects and nectar. We could not be sure what they were feeding the young. Defence of the nest varied with the position of the female and the type of intruder. The aggressive behaviour associated with defence varied according to the size and type of intruder. We concluded that for the one nest of Eulampis for which we had the most complete data, had there been three young, the female would have been unable to provide sufficient food to nourish them. However, the universal clutch size of two and nearly universal promiscuity in humming- birds is strong evidence that factors other than the ability of adults to feed more than two young are important in determining clutch size.     

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.     

Why do grebes cover their nests? Laboratory and field tests of two alternative hypotheses

Egg predation is a common feature influencing the reproductive success of open nesting birds. Evolutionary pressure therefore favours building cryptic, inconspicuous nests. However, these antipredatory pressures may be in conflict with thermoregulatory constraints, which select for dry nest material maintaining optimum temperature inside a nest cup during the absence of incubating parents. Here we examined possible trade-offs between nest crypsis and thermoregulation in Little Grebes (Tachybaptus ruficollis), which lay their eggs in floating nests built from wet plant material. As this species regularly covers its eggs with nest material, we experimentally examined (1) the rates of egg predation on covered and uncovered artificial nests and (2) possible thermoregulatory costs from nest covering by comparing temperature and relative humidity changes inside the nest cup. Results revealed that covering clutches is beneficial in terms of deterring predators, because uncovered eggs were more vulnerable to predation. Moreover, covering clutches also had thermoregulatory benefits because the mean temperature and relative humidity inside nest cups covered by dry or wet materials were significantly higher for covered compared to uncovered treatments. Covering clutches in Little Grebes therefore does not pose thermoregulatory costs.     

FIELD-NOTES ON NIDIFICATION AND DISTRACTION-DISPLAY IN THE GOLDEN PLOVER

Data for the Golden Plover Pluvialis apricaria , breeding in the Faeroe Islands, suggest that the species is more successful up to. and including the hatching phase than the Whimbrel Numenius ph. phœopus. Oyster-catcher Hœmatopus ostralegus occidentalis , and Faeroe Snipe Capella gallinago faeroeensis. Comparative figures for average clutch, young leaving the nest, and losses due to predators, infertility, etc., are given for a small number of nests.
Simultaneous hatching is more general than in the Whimbrel and the hatching-period, normally about 100 hours, is some 10–20 hours less. Detailed records of hatching are given in the case of seven nests.
Field-notes are given on the nuptial flight, and a "partnership-run" is described.
Both sexes share incubation and care of the young, the family quickly deserting the nesting-site. Shell remains are removed and young hatched late in the day appear to pass the night on the nest.
In distraction-display an aggressive form was not recorded, but stationary and moving "lure displays" of three distinct kinds (in addition to the normal run from the nest or young) are described. A case is cited in which the male, when flushed from eggs, directed the "lure-display" at its mate.     

Potential influences of climate and nest structure on spotted owl reproductive success: a biophysical approach

Many bird species do not make their own nests; therefore, selection of existing sites that provide adequate microclimates is critical. This is particularly true for owls in north temperate climates that often nest early in the year when inclement weather is common. Spotted owls use three main types of nest structures, each of which are structurally distinct and may provide varying levels of protection to the eggs or young. We tested the hypothesis that spotted owl nest configuration influences nest microclimate using both experimental and observational data. We used a wind tunnel to estimate the convective heat transfer coefficient (h(c)) of eggs in 25 potential nest configurations that mimicked 2 nest types (top-cavity and platform nests), at 3 different wind speeds. We then used the estimates of h(c) in a biophysical heat transfer model to estimate how long it would take unattended eggs to cool from incubation temperature (～36°C) to physiological zero temperature (PZT; ～26°C) under natural environmental conditions. Our results indicated that the structural configuration of nests influences the cooling time of the eggs inside those nests, and hence, influences the nest microclimate. Estimates of time to PZT ranged from 10.6 minutes to 33.3 minutes. Nest configurations that were most similar to platform nests always had the fastest egg cooling times, suggesting that platform nests were the least protective of those nests we tested. Our field data coupled with our experimental results suggested that nest choice is important for the reproductive success of owls during years of inclement weather or in regions characterized by inclement weather during the nesting season.     

Herbaceous ground cover reduces nest predation in olive groves

Capsule Bare ground increases artificial nest predation in olive groves.

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

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

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

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

Nest construction by a ground-nesting bird represents a potential trade-off between egg crypticity and thermoregulation

Predation selects against conspicuous colors in bird eggs and nests, while thermoregulatory constraints select for nest-building behavior that regulates incubation temperatures. We present results that suggest a trade-off between nest crypticity and thermoregulation of eggs based on selection of nest materials by piping plovers (Charadrius melodus), a ground-nesting bird that constructs simple, pebble-lined nests highly vulnerable to predators and exposed to temperature extremes. Piping plovers selected pebbles that were whiter and appeared closer in color to eggs than randomly available pebbles, suggesting a crypsis function. However, nests that were more contrasting in color to surrounding substrates were at greater risk of predation, suggesting an alternate strategy driving selection of white rocks. Near-infrared reflectance of nest pebbles was higher than randomly available pebbles, indicating a direct physical mechanism for heat control through pebble selection. Artificial nests constructed of randomly available pebbles heated more quickly and conferred heat to model eggs, causing eggs to heat more rapidly than in nests constructed from piping plover nest pebbles. Thermal models and field data indicated that temperatures inside nests may remain up to 2–6°C cooler than surrounding substrates. Thermal models indicated that nests heat especially rapidly if not incubated, suggesting that nest construction behavior may serve to keep eggs cooler during the unattended laying period. Thus, pebble selection suggests a potential trade-off between maximizing heat reflectance to improve egg microclimate and minimizing conspicuous contrast of nests with the surrounding substrate to conceal eggs from predators. Nest construction behavior that employs light-colored, thermally reflective materials may represent an evolutionary response by birds and other egg-laying organisms to egg predation and heat stress. An erratum to this article can be found at     

Appearance and vulnerability of artificial duck nests to avian predators

Use of artificial nests in studies of nest success in birds has become increasingly popular, but this practice has been criticised because the appearance and success of artificial nests may differ from natural nests. Typically, artificial nests are presented with few visible eggs throughout the entire exposure period while natural nests during their life have different appearances, possibly producing stage-dependent predation rates. In ducks, nests may appear with openly visible eggs, eggs covered with nest material and covered by an incubating female. To test how nest appearance may affect nest survival, I simulated such duck nest appearances, and used direct observations to record responses of marsh harriers Circus aeruginosus , the dominant duck nest predator at the Lake Engure, Latvia, during the breeding seasons 2000–2002. I recorded 274 harrier flights over all types of artificial nests, 74 nest discoveries and 54 predation events. Logistic regression analyses showed that nest appearance was a significant predictor of the fate of the nest: nests with openly visible eggs were discovered more often than nests covered with nest material. Nests with dummy females had discovery rates similar to the average of all artificial nest types suggesting that they best reflect the predation risk of artificial nests and could be used in future studies. After discovering nests covered with dummy females, harriers never attacked but tried to scare them off to get access to the eggs. In 52% of cases of nest discovery, harriers gave up before touching the dummy. This shows that duck passive nest defence may prevent clutch predation.     

朱鹮(Nipponia nippon)的繁殖习性

文章概述了朱鹮的濒危状况及陕西省洋县1981—1986年的繁殖数量,计6年9窝27幼,已知死亡4只,人工喂养3只。 朱鹮在洋县为留鸟,越冬期间偶尔返回繁殖地,2月中旬后不再离开。有显著的领域性。3月上旬开始营巢,中旬至4月初产卵,多数3枚(1—4枚)。孵卵期30天左右,育雏期约为40天,均由雌雄亲鸟共同承担。6月中下旬全窝育成后一起飞离巢区。     

Larger clutch size increases fledging success and offspring quality in a precocial species

1. We tested the hypothesis that the ability of parents to raise viable offspring limits clutch size in the greater snow goose ( Anser caerulescens atlanticus L.), a precocial bird.
2. We manipulated clutch size by exchanging complete clutches between pairs of nests to increase or decrease the clutch size by zero (control), one, two or three eggs in 314 nests over 2 years.
3. Pre-fledging survival of goslings increased in enlarged broods and decreased in reduced broods compared to control. Consequently, enlarged broods fledged more offspring and the reverse was true for reduced broods.
4. Size and mass of goslings near fledging was also higher in enlarged broods than in control, which suggests that offspring quality was also enhanced by the manipulation. This is contrary to the common trade-off between offspring numbers and quality.
5. Large families were dominant over smaller ones in feeding sites, which could explain the increased survival and growth of enlarged broods.
6. Our results suggest that the ability to raise young does not limit clutch size in this species and that parents could be more successful (i.e. increase both the number and quality of their offspring) by laying more eggs. However, the time required to lay additional eggs reduces the viability of all offspring and may explain why females do not lay more eggs.     

Using artificial nests to predict nest survival at reintroduction sites

Artificial nests are frequently used to assess factors affecting survival of natural bird nests. We tested the potential for artificial nests to be used in a novel application, the prediction of nest predation rates at potential reintroduction sites where exotic predators are being controlled. We collected artificial nest data from nine sites with different predator control regimes around the North Island of New Zealand, and compared the nest survival rates with those of North Island robin (Petroica longipes) nests at the same sites. Most of the robin populations had been reintroduced in the last 10 years, and were known to vary in nest survival and status (increasing/stable or declining). We derived estimates of robin nest survival for each site based on Stanley estimates of daily survival probabilities and the known incubation and brooding periods of robins. Estimates of artificial nest survival for each site were derived using the known fate model in MARK. We identified the imprints on the clay eggs in the artificial nests, and obtained different estimates of artificial nest survival based on imprints made by different potential predators. We then compared the value of these estimates for predicting natural nest survival, assuming a relationship of the form s = αpβ, where s is natural nest survival and p is artificial nest survival. Artificial nest survival estimates based on imprints made by rats (Rattus spp.) and brushtail possums (Trichosurus vulpecula) were clearly the best predictors (based on AICc), and explained 64% of the variation in robin nest survival among sites. Inclusion of bird imprints in the artificial nest survival estimates substantially reduced their predictive value. We suggest that artificial nests may provide a useful tool for predicting the suitability of potential reintroduction sites for New Zealand forest birds as long as imprints on clay eggs are correctly identified.     

Reproductive allocation in multinest colonies of the ponerine ant Pachycondyla goeldii

Abstract.  1.  Pachycondyla goeldii constitutes the only recorded case of a monogynous (i.e. one queen per colony) polydomous (i.e. several nests per colony) species in the Ponerinae subfamily. This study examines the impact of polydomy on reproductive allocation between nests (also called 'calies' in polydomous society) in Pachycondyla goeldii Forel, by: (i) recording the number of workers and sexuals in 67 nests belonging to 21 colonies; (ii) dissection of workers in nine nests containing a queen (QR nests), nine nests without a queen but associated to a QR nest (QL nests) and five nests belonging to colonies that permanently lost the queen (OR nests); and (iii) measuring the length of all eggs present in the nests (our laboratory study shows that queen-laid eggs were significantly longer than worker-laid eggs).
2. The number of workers was significantly higher in QR nests than in QL nests, while the number of virgin queens was significantly higher in QL nests compared with QR nests.
3. Worker ovarian activity is inversely related to queen proximity: highest in OR nests, intermediate in QL nests, and lowest in QR nests.
4. Egg length was highest in QR nests, where the queen was most likely the primary egg-layer, intermediate in QL nests, where eggs could have originated from both the queen and workers, and lowest in OR nests, where workers were the sole egg-layers.
5. We postulate that the proximal mechanism explaining differences between QR and QL nests is the pheromonal absence of the queen from QL nests and that the evolutionary reasons of these divergences between nest types are likely to originate from the different conflicts occurring in ant colonies.     

Nest orientation of the Spotted Barbtail, <Emphasis Type="Italic">Premnoplex brunnescens</Emphasis>, is strongly correlated with stream flow

The placement and orientation of bird nests may strongly influence reproductive success. For many species, nest orientation is related to the cardinal directions and has to do with prevailing winds or solar exposure. Nest orientation differs among species in different environments, variously cooling or warming nests to maintain a nest microclimate optimal for successful development of eggs and young. The Spotted Barbtail (Premnoplex brunnescens) builds mossy, enclosed nests along shaded streams in Neotropical cloud forests. It shows a unique pattern of nest orientation, whereby nests are oriented in relation to the direction of water flowing below the nest entrance, rather than compass bearing. Nests face in one of three directions in relation to the stream: downstream, upstream, or perpendicular to the flow of the water. I discuss the ability of various hypotheses to explain this pattern in the context of factors affecting nest orientation in other species. While the reasons for this pattern of orientation remain unclear, orientation is likely driven by the need to create and maintain an optimal internal nest microclimate.     

Factors affecting nesting success in the Great-crested Grebe Podiceps cristatus at Lake Tonga,north-east Algeria

The breeding ecology of the Great-crested Grebe Podiceps cristatus was investigated over four consecutive years (2009-2012) at Lake Tonga, north-east Algeria. In all four years, the egg-laying period was relatively short, spanning two months (end of March to end of May), and bimodal. Nests were mainly located in Phragmites australis, over water of substantial depth (178 ± 43?cm, N=209), far from the shore and in habitat with low vegetation cover (12.37 ± 7.67%, N=209). The overall clutch size was 3.73 ± 0.92 eggs (N=127) and it decreased marginally over time. The overall nesting success was 70.4% (N=209), with nest failure caused mainly by predation (65%) and flooding (23%). Breeding outcome was significantly and positively related to nest size, with bigger nests conferring better survival to eggs and young probably through affording better protection during spells of adverse weather. However, the benefits of bigger nests may be confounded by the age or intrinsic quality of birds. The location of nests in P. australis, rather than other vegetation types, increased nesting success marginally but significantly. Two cases of interspecific mixed clutches involving the Great-crested Grebe were recorded.     

Predation of artificial nests by introduced rhesus macaques (<Emphasis Type="Italic">Macaca mulatta</Emphasis>) in Florida,USA

Native throughout Asia, rhesus macaques are believed to have the widest native range of any non-human primate and are capable of adapting to an extensive diversity of habitats. Rhesus macaques have caused environmental degradation in introduced habitats, including decreasing bird populations through nest predation. In the 1930s, rhesus macaques were intentionally introduced into what is today Silver Springs State Park (SSSP), central Florida, in an effort to increase tourism. Our objective was to determine whether introduced rhesus macaques in SSSP would consume eggs presented in artificial nests. We used camera traps adjacent to 100 open-cupped artificial bird nests baited with quail eggs near the Silver River. Nests were placed in shrubs and left in the field site for 12 days, representative of the incubation period of native passerine species. Twenty-one nests were depredated by rhesus macaques, nine by nest predators other than macaques, and five nests by an unidentified predator. Nests were more likely to be depredated by macaques when located in areas of high macaque relative abundance. This study suggests introduced rhesus macaques may influence nest predation rates of native bird species in natural areas.     

Composition of Bacterial Assemblages in Different Components of Reed Warbler Nests and a Possible Role of Egg Incubation in Pathogen Regulation

Bacteria play a central role in animal health. Yet, little is known about the acquisition of bacteria and the extent to which bacteria are acquired from different environmental sources. For example, bird nests host diverse bacteria associated with the eggs, nestlings and nesting material, but previous research has typically focussed on only a limited number of nest components at a time. It therefore remains unknown to what extent bacteria are transmitted between these components. Using both molecular and culture techniques, we characterised nest-associated bacterial assemblages throughout the entire nesting cycle of reed warblers by sampling bacteria on eggs before and during incubation, within nestling faeces, and on the nesting material of post-breeding nests. We found that bacterial assemblages clustered by nest component. Yet some overlap existed between nest components, suggesting that bacterial transmission across components is likely to occur. Eggs and nestlings from the same nest harboured more similar bacteria than expected by chance, suggesting an influence of environment or genetics on bacterial assemblages. Bacterial loads were not lower on incubated eggs. Instead, incubation was associated with a change in the structure of assemblages, including a decrease in potentially-harmful Gram-negative bacteria. In addition we show for the first time, that incubation is associated with the complete extinction of harmful haemolytic bacteria. Overall, our study appears to be the first to demonstrate differences in bacterial assemblages between bird nest components. In addition, we highlight the complexity of nest bacterial assemblages and provide new insights into the benefits of incubation.     

Costs and response to conspecific brood parasitism by colonial red-breasted mergansers

Costs of conspecific brood parasitism (CBP) are expected to be influenced by a species’ life history traits. Precocial birds lay large clutches, and clutches that have been enlarged by CBP can affect host fitness through a longer incubation period, displaced eggs, and lower hatching success. We examined costs and response to CBP by hosts in a population of colonial red-breasted mergansers (Mergus serrator; n?=?400 nests over 8 years) within which 29% of parasitized clutches were enlarged considerably (≥?15 eggs). Length of the incubation period did not increase with clutch size. The mean number of eggs displaced from a parasitized nest during incubation (2.8) was 2×?greater than at an unparasitized nest (1.4). Hatching success declined by 2% for each additional egg in the nest. Thus, for a nest with?≥?15 eggs, one or more fewer host eggs hatch relative to an unparasitized nest with the same number of host eggs, assuming equal probability of success for all eggs. Hosts were 40% more likely to desert nests receiving 2 or 6 experimental eggs relative to unparasitized control nests, although it is unknown whether hens deserting a nest renested elsewhere. Our study indicates that costs of CBP to hosts during nesting may be limited to those red-breasted mergansers incubating the largest clutches (≥?15 eggs), and it raises questions about the adaptive significance of deserting a parasitized clutch.     

Incubation rhythm in the great snipe Gallinago media

The incubation rhythm of four female great snipe was monitored with telemetric equipment. The mean daily incubation constancy was 90.3 ± 2.0 (SD) per cent, and the mean daily time off the nest amounted to 139.8 ± 28.8 min. The number of recesses per day averaged 8.7 ± 1.9, with a mean duration of 15.7 ± 6.1 min. Generally, the birds incubated for long bouts during the night, and left the nest frequently during the daylight hours.
Recesses were concentrated in the warmest part of the day in cool periods, but were more evenly distributed throughout the day in warmer periods. Recess duration decreased with decreasing temperature. These adjustments minimize egg cooling when the bird is off the nest, and thus allow the incubating bird more time to feed without lowering the mean egg temperature.
Calculations of the cooling rates of eggs indicate that the bird minimizes incubation energy expenditure as far as possible, but without letting the eggs cool beyond the temperature of no embryonic development.     

Nest height, nest concealment, and predator type predict nest predation in superb fairy-wrens (Malurus?cyaneus)

Three factors and their interaction effects are increasingly recognized as important determinants of nest predation: nest concealment, nest height, and predator type. The risk of nest predation is predicted to vary across these variables because of nest detectability and accessibility. In general, however, few studies examine how these three variables interact in relation to nest predation, focusing instead on either nest concealment or nest height (whereby predator identity is usually not known). In this study, we examine the role of nest concealment and nest height for nest survival using both artificial and natural nests in the superb fairy-wren (Malurus cyaneus). We indirectly identified potential predators through marks left on artificial eggs and footprints left on tracking tunnels. Predation level at artificial nests was lower than at natural nests, and this could be due to a failure of some nest predators to locate cryptic nests in the absence of cues provided by parental activity. Our results supported the prediction that exposed and concealed nests have different levels of nest predation, which can be explained by variation in predator type. Visual predators were only detected at exposed nests, and survival from visual predators was lower for high nests that were also exposed. However, olfactory predators were detected irrespective of nest height or nest concealment. Because rodents use olfaction to locate nests, this could explain the lack of association between nest concealment and predation outcome at low nests. In addition, rodent footmarks near nests were significantly associated with rodent tooth marks on eggs.