Diesj?hrige Wiesenpieper(Anthus pratensis) als Helfer am Nest

Summary On 23.7. 1977a colour-ringed first-year Meadow Pipit was observed feeding nestlings of a third brood of more than two-year-old parent Meadow Pipits for at least three times. The first-year Meadow Pipit had hatched about 1.5. 1977 in a nest about 3100m off the place where it helped feeding.On 27. and 28.6. 1978 another first-year Meadow Pipit was observed feeding nestlings of a brood some four times. This first-year Meadow Pipit had hatched about 8.5. 1978 nearly 3400m off the place where it helped feeding. The only adult parent that was seen feeding the brood was a colour-ringed adult male. On 14.6. 1978 a copulation was observed between the adult male and the first-year Meadow Pipit — obviously a female.Evidently there were no close relationships between the first-year Meadow Pipits and the parents of the broods they helped.     

Habitat associations of breeding Meadow Pipits Anthus pratensis in the British uplands

Habitat associations of Meadow Pipits breeding in British upland 1 km and 10 km squares were investigated using data from the British Trust for Ornithology's (BTO) Breeding Bird Survey (BBS, 1994–97), The New Atlas of Breeding Birds in Britain and Ireland 1988–1991 and habitat data from the Institute of Terrestrial Ecology's (ITE) Land Cover Survey (1994). Meadow Pipit density was highest in 200 m sections of BBS 1 km transects containing unenclosed grass moor, heather and bog, but there was no difference in Meadow Pipit density between these habitat types. Meadow Pipit density (number of individuals per 1 km square) increased with heather cover up to about 7.5 200 m sections (of ten per 1 km square) of heather, but fell thereafter. There was a positive association between Meadow Pipit density and the extent of grass moor cover. The ITE Land Cover data gave results that were consistent with the BBS habitat data at both the 1 km and 10 km square scale. There was a non-linear relationship between hill grass cover and Meadow Pipit abundance, which reached a maximum when hill grass covered between 40%and 60% of a square. Our results suggest that a mosaic of heather, bog and grassland may be the optimum habitat for Meadow Pipits. Recent changes in land management practices may have led to the disappearance or degradation of these mosaics in some areas. Meadow Pipits are widespread and easily counted. We suggest that this species might be a useful bioindicator of changes in heather and grassland ratios that result from land management practices such as grazing and rotational burning, though further research is required.     

The breeding biology of the endemic Berthelot's Pipit Anthus berthelotii in a harsh oceanic island environment (Tenerife,Canary Islands)

We describe the density, breeding and foraging ecology of the Berthelot's Pipit (Anthus berthelotii), an endemic passerine to the Atlantic islands, in the semi-arid coastal scrub of Tenerife. Furthermore, we analyse the effects of temperature and rainfall in the onset of reproduction and the behaviour (nest site and foraging site selection). The average density of the Pipit (using DISTANCE methodology) in the semi-arid coastal scrub was 7.1 birds 10ha^?1, and the overall density estimate in grassland was 3.3 birds 10ha^?1. The Pipit bred early (mean average first-egg laying date 12 February) and in response to rainfall (but not temperature). By the Mayfield method, the probability of the nests surviving the egg stage was 0.77 and of and the nests surviving the chick stage 0.67 — assuming an incubation period of 13 days and a chick stage of 12.5 days — based on the European average for the similar-sized Meadow Pipit Anthus pratensis. Overall nest survival pooling stages were 0.51. The Pipits had a low clutch size (3.3 eggs, range of 2–4). Nest damage by heavy rainstorms was the major cause of nest failures (three out of five failures). The Pipits nested preferentially in grass with relatively low densities of Euphorbia balsamifera bushes. Birds selected grassy areas as their main foraging site but also preferred to forage on large rocks during nesting: caterpillars were the main food items (14 out of 17 prey captures).     

Buildings promote higher incubation temperatures and reduce nest attentiveness in a Neotropical thrush

Incubation is an energetically costly parental task of breeding birds. Incubating parents respond to environmental variation and nest‐site features to adjust the balance between the time spent incubating (i.e. nest attentiveness) and foraging to supply their own needs. Non‐natural nesting substrates such as human buildings impose new environmental contexts that may affect time allocation of incubating birds but this topic remains little studied. Here, we tested whether nesting substrate type (buildings vs. trees) affects the temperature inside the incubation chamber (hereafter ‘nest temperature’) in the Pale‐breasted Thrush Turdus leucomelas, either during ‘day’ (with incubation recesses) or ‘night’ periods (representing uninterrupted female presence at the nest). We also tested whether nesting substrate type affects the incubation time budget using air temperature and the day of the incubation cycle as covariates. Nest temperature, when controlled for microhabitat temperature, was higher at night and in nests in buildings but did not differ between daytime and night for nests in buildings, indicating that buildings partially compensate for incubation recesses by females with regard to nest temperature stability. Females from nests placed in buildings exhibited lower nest attentiveness (the overall percentage of time spent incubating) and had longer bouts off the nest. Higher air temperatures were significantly correlated with shorter bouts on the nest and longer bouts off the nest, but without affecting nest attentiveness. We suggest that the longer bouts off the nest taken by females of nests in buildings is a consequence of higher nest temperatures promoted by man‐made structures around these nests. Use of buildings as nesting substrate may therefore increase parental fitness due to a relaxed incubation budget, and potentially drive the evolution of incubation behaviour in certain urban bird populations.     

Predictive mapping of Meadow Pipit density using integrated remote sensing data and an atlas of vascular plants dataset

Capsule The highest densities of Meadow Pipits in Central Europe are found in lowland and upland wet meadows.

Aims To create a large-scale predictive model of Meadow Pipit density.

Methods We analysed factors affecting the density of the Meadows Pipit in Poland using data from 777?×?1?km study plots and a set of 22 environmental variables, including agriculture intensification and habitat-specific plant species as classifiers of meadow types. Predictors were selected using variation inflation factor, then related to species density data using generalized additive models.

Results The best-supported model included 11 variables and was clearly better (Akaike information criterion weight?=?0.47) than other models. The density of the Meadow Pipit reaches its highest levels on large areas of extensively used wet meadows as well as pastures where livestock graze and which show high photosynthetic activity in April.

Conclusion Some aspects of the environment that were not identified from remote sensing data were vital for determining relatively high density. Conservation efforts for preserving Meadow Pipit populations should focus on maintaining wet meadows and extensively grazed pastures. Given the results, the Meadows Pipit may be classified as a good indicator of traditional agriculture.     

Night conditions affect morning incubation behaviour differently across a latitudinal gradient

Intermittently incubating birds alternate between sessions of egg warming and recesses for foraging during the day, but stay on the nest continuously at night. Hence, energy costs of nocturnal incubation (which increase during longer and colder nights) cannot be replenished until the next day. Night conditions might therefore be expected to affect morning incubation behaviour the day after. We tested this prediction by exploring latitudinal and seasonal trends in characteristics of the first recess in Eastern Bluebirds Sialia sialis over a 1400-km latitudinal gradient in the continental USA. The time from civil dawn to leaving the nest (latency) increased with latitude early in the breeding season but decreased with latitude late in the season. Birds breeding at higher latitudes also took longer first recesses throughout the season, which led to a larger drop in nest temperature. At the local scale, birds rose earlier after longer nights if the night was also cold, but night length did not predict latency following warm nights. The first recess was longer if the night was warmer, probably because birds could replenish reserves at lower risk of low egg temperature. Our study shows that characteristics of the night led to behavioural changes in features of early morning incubation that were evident at both continental and local scales. These responses also affected nest temperature. Hence, night conditions carry over to incubation behaviour the following morning, which in turn may impose thermal constraints on embryonic development.     

Interrupted incubation: How dabbling ducks respond when flushed from the nest

Nesting birds must provide a thermal environment sufficient for egg development while also meeting self‐maintenance needs. Many birds, particularly those with uniparental incubation, achieve this balance through periodic incubation recesses, during which foraging and other self‐maintenance activities can occur. However, incubating birds may experience disturbances such as predator or human activity which interrupt natural incubation patterns by compelling them to leave the nest. We characterized incubating mallard Anas platyrhynchos and gadwall Mareca strepera hens’ responses when flushed by predators and investigators in Suisun Marsh, California, USA. Diurnal incubation recesses initiated by investigators approaching nests were 63% longer than natural diurnal incubation recesses initiated by the hen (geometric mean: 226.77 min versus 142.04 min). Nocturnal incubation recesses, many of which were likely the result of predators flushing hens, were of similar duration regardless of whether the nest was partially depredated during the event (115.33 [101.01;131.68] minutes) or not (119.62 [111.96;127.82] minutes), yet were 16% shorter than natural diurnal incubation recesses. Hens moved further from the nest during natural diurnal recesses or investigator‐initiated recesses than during nocturnal recesses, and the proportion of hen locations recorded in wetland versus upland habitat during recesses varied with recess type (model‐predicted means: natural diurnal recess 0.77; investigator‐initiated recess 0.82; nocturnal recess 0.31). Hens were more likely to take a natural recess following an investigator‐initiated recess earlier that same day than following a natural recess earlier that same day, and natural recesses that followed an investigator‐initiated recess were longer than natural recesses that followed an earlier natural recess, suggesting that hens may not fulfill all of their physiological needs during investigator‐initiated recesses. We found no evidence that the duration of investigator‐initiated recesses was influenced by repeated visits to the nest, whether by predators or by investigators, and trapping and handling the hen did not affect investigator‐initiated recess duration unless the hen was also fitted with a backpack‐harness style GPS–GSM transmitter at the time of capture. Hens that were captured and fitted with GPS–GSM transmitters took recesses that were 26% longer than recesses during which a hen was captured but a GPS–GSM transmitter was not attached. Incubation interruptions had measurable but limited and specific effects on hen behavior.     

Blow fly Trypocalliphora braueri parasitism on Meadow Pipit and Bluethroat nestlings in Central Europe

The larvae of blow fly (Trypocalliphora braueri) are known to cause a subcutaneous myiasis in bird nestlings mainly in Nearctic species, while only a few records are available from the Palaearctic. Here, we report on infestations of this insect ectoparasite in two passerine species, Meadow Pipit (Anthus pratensis) and Bluethroat (Luscinia svecica), breeding in the Central European mountain range Krkonoše. The infestation of T. braueri parasite was relatively low in studied bird species (3.0% of infested nests in Meadow Pipit and 4.2% in Bluethroat) but varied strongly between years (0–33% of infested nests/year/species). The presence of the parasitic blow fly larvae was apparently controlled by temperature; they were found only during warm summers. The combination of parasite infection and heavy rainfalls in a critical period significantly reduced nestling survival.     

Factors influencing nocturnal egg-turning frequency in Meadow Pipits Anthus pratensis

Capsule Mean frequency of nocturnal egg-turning in Meadow Pipits is similar to that found in other passerines. Turning frequency changes during incubation, with time since the start of incubation exerting the strongest influence.     

The phylogenetic relationships of Berthelot's Pipit Anthus berthelotii illustrated by DNA sequence data, with remarks on the genetic distance between Rock and Water Pipits Anthus spinoletta

The phylogenetic relationships of Berthelot's Pipit Anthus berthelotii , which is endemic to three groups of North Atlantic islands, have puzzled ornithologists for more than a century. A total of 1041 base pair cytochrome b mitochondrial DNA sequences from Berthelot's Pipit are compared with homologous sequences from the Tawny Pipit Anthus campestris , Richard's Pipit Anthus novaeseelandiae , the Meadow Pipit Anthus pratensis , the Red-breasted Pipit Anthus cervinus , the Tree Pipit Anthus trivialis , Rock and Water Pipits Anthus spinoletta and the White Wagtail Motacilla alba. In the resulting phytogeny, the sister taxon of Berthelot's Pipit is unambiguously the Tawny Pipit, with Richard's Pipit forming a deeper branch on the same clade. Sequences of a Danish Rock Pipit and a Swiss Water Pipit support a close relationship between these two species, but more comprehensive studies of intra- and interpopulation variation are required before considering their taxonomic ranking. Some preliminary inferences are made regarding phylogenetic tendencies in the genus Anthus.     

Factors influencing Cinnamon Teal nest attendance patterns

Patterns of nest attendance in birds result from complex behaviours and influence the success of reproductive events. Incubation behaviours vary based on individual body condition, energy requirements and environmental factors. We assessed nest attendance patterns in Cinnamon Teal Spatula cyanoptera breeding in the San Luis Valley of Colorado in 2016–2017 using trail and video cameras to observe behaviours throughout incubation. We evaluated the effect of temporal, life‐history and environmental covariates on the frequency and duration of incubation recesses as well as the incubation constancy. There was considerable model uncertainty among the models used to evaluate recess frequency. Recess duration varied according to the interaction between nest age and a quadratic effect of time of day, with hens on older nests taking longer recesses in the afternoon and hens on nests earlier in incubation taking longer recesses in the morning and evening. Incubation constancy decreased with higher ambient temperatures in the study area. This study provides evidence that Cinnamon Teal modify their behaviour during incubation according to the age of the nest and the time of day. These results improve our knowledge of Cinnamon Teal breeding ecology and shed light on the behaviours that fast‐lived species may use to cope with environmental factors during nesting.     

Diet composition influences annual breeding success of Montagu's Harriers Circus pygargus feeding on diverse prey

Capsule Three similarly sized passerine species with various breeding strategies behaved differently in the presence of models of mammalian and avian predators.

Aims We tested whether solitary breeders behave in the presence of a predator in order to avoid disclosing their nest site in: hole-nesting Pied Flycatcher Ficedula hypoleuca, shrub-nesting Blackcap Sylvia atricapilla and ground-nesting Meadow Pipit Anthus pratensis.

Methods The behaviour of parents in response to two types of predator model (visually oriented Corvid birds and olfactory oriented Mustelid mammals) placed sequentially at 40, 5 and 1 m distance from the nest was recorded from a shelter.

Results The hypothesis was supported in open-nesting species (Meadow Pipit and Blackcap), as parents did not approach the nest in the presence of a predator. In the hole-nesting Pied Flycatcher the parents disclosed the nest site in most cases (by entering the nest). The intensity of alarm calling increased with decreasing distance of a predator from the nest in all species except Meadow Pipit in the presence of Raven Corvus corax models. The intensity of attacking changed only in Meadow Pipit with decreasing distance of Stoat Mustela erminea from the nest.

Conclusion The results showed that anti-predator behaviour was species-specific, depending on type of predator, habitat and nest inaccessibility.     

Timing,frequency, and duration of incubation recesses in dabbling ducks

Nest attendance is an important determinant of avian reproductive success, and identifying factors that influence the frequency and duration of incubation recesses furthers our understanding of how incubating birds balance their needs with those of their offspring. We characterized the frequency and timing (start time, end time, and duration) of incubation recesses for mallard (Anas platyrhynchos) and gadwall (Mareca strepera) hens breeding in Suisun Marsh, California, USA, and examined the influences of day of year, ambient temperature at the nest, incubation day, and clutch size on recess frequency and timing using linear mixed models. Mallard, on average, took more recesses per day (1.69 ± 0.80, mean ± standard deviation) than did gadwall (1.39 ± 0.69), and 45% of mallard nest‐days were characterized by two recesses, while only 27% of gadwall nest‐days were characterized by two recesses. Mallard morning recesses started at 06:14 ± 02:46 and lasted 106.11 ± 2.01 min, whereas mallard afternoon recesses started at 16:39 ± 02:11 and lasted 155.39 ± 1.99 min. Gadwall morning recesses started at 06:30 ± 02:46 and lasted 91.28 ± 2.32 min, and gadwall afternoon recesses started at 16:31 ± 01:57 and lasted 192.69 ± 1.89 min. Mallard and gadwall started recesses earlier in the day with increasing ambient temperature, but later in the day as the season progressed. Recess duration decreased as the season progressed and as clutch size increased, and increased with ambient temperature at the nest. The impending darkness of sunset appeared to be a strong cue for ending a recess and returning to the nest, because hens returned to their nests earlier than expected when recesses were expected to end after sunset. Within hens, the timing of incubation recesses was repeatable across incubation days and was most repeatable for mallard afternoon recesses and on days in which hens took only one recess. Hens were most likely to be away from nests between 04:00 and 07:00 and between 16:00 and 19:00; therefore, investigators should search for nests between 07:00 and 16:00. Our analyses identified important factors influencing incubation recess timing in dabbling ducks and have important implications for nest monitoring programs.     

Do pipits use experimentally supplemented rich sources of calcium more often in an acidified area?

How birds respond to the recent phenomenon of calcium deficiency in acidified areas is still poorly known. This study, carried out in the Jeseníky Mountains (heavily polluted, acidified area in the Czech Republic), in alpine ecosystems of central Norway, and in the limestone part of the Malá Fatra Mountains (Slovak Republic), provides the first experimental evidence that birds select and bring supplemented calcium-rich items to their nestlings more often in an acidified area. Meadow Pipits Anthus pratensis and Water Pipits A. spinoletta selected calcium-rich items (mainly snail shells) from various materials placed near their nests and this selectivity did not differ between areas or species. Thinning of egg shells (8% at blunt pole, 5% at egg side) suggests that Meadow Pipits in the Jeseníky Mountains were negatively influenced by the low calcium availability, in spite of their ability to adjust foraging behaviour.     

Do extended incubation recesses carry fitness costs in two cavity‐nesting birds?

Because extended incubation recesses, where incubating songbirds are away from nests for periods much longer than usual, occur infrequently, they have been treated as outliers in most previous studies and thus overlooked. However, egg temperatures can potentially fall below the physiological zero temperature during extended recesses, potentially affecting developing embryos. As such, evaluating extended recesses in an ecological context and identifying their possible fitness effects are important. With this aim, we used iButton data loggers to monitor the incubation behavior of female Blue Tits (Cyanistes caeruleus) and Great Tits (Parus major) during two breeding seasons in central Spain. We classified incubation recesses as extended if they were more than four times the mean recess duration for each species. Extended incubation recesses occurred more frequently in 2012 when females exhibited poorer body condition. Female Blue Tits had more extended incubation recesses than female Great Tits and, for both species, more extended recesses occurred at the beginning of the breeding season. Both nest attentiveness and average minimum nest temperature decreased when at least one extended recess occurred. Incubation periods averaged 4 d longer for nests where females had at least one extended recess, potentially increasing predation risk and resulting in lower‐quality nestlings. Overall, our results suggest that extended recesses may be more common among songbirds than previously thought and that, due to their effects on egg temperatures and attentiveness, they could impose fitness costs.     

Incubation behavior of king eiders on the coastal plain of northern Alaska

Incubating birds balance their energetic demands during incubation with the needs of the developing embryos. Incubation behavior is correlated with body size; larger birds can accumulate more endogenous reserves and maintain higher incubation constancy. King eiders (Somateria spectabilis) contend with variable and cold spring weather, little nesting cover, and low food availability, and thus are likely to rely heavily on endogenous reserves to maintain high incubation constancy. We examined the patterns of nest attendance of king eiders at Teshekpuk and Kuparuk, Alaska (2002–2005) in relation to clutch size, daily temperature, and endogenous reserves to explore factors controlling incubation behavior. Females at Kuparuk had higher constancy (98.5 ± 0.2%, n = 30) than at Teshekpuk (96.9 ± 0.8%, n = 26), largely due to length of recesses. Mean recess length ranged from 21.5 to 23.7 min at Kuparuk, and from 28.5 to 51.2 min at Teshekpuk. Mean body mass on arrival at breeding grounds (range; Teshekpuk 1,541–1,805, Kuparuk 1,616–1,760), and at the end of incubation (Teshekpuk 1,113–1,174, Kuparuk 1,173–1,183), did not vary between sites or among years (F < 1.1, P > 0.3). Daily constancy increased 1% with every 5°C increase in minimum daily temperature (β _min = 0.005, 95% CI 0.002, 0.009). Higher constancy combined with similar mass loss at Kuparuk implies that females there met foraging requirements with shorter recesses. Additionally, females took more recesses at low temperatures, suggesting increased maintenance needs which were potentially ameliorated by feeding during these recesses, indicating that metabolic costs and local foraging conditions drove incubation behavior.     

Incubation pattern and foraging effort in the female Water Pipit Anthus spinoletta

Incubation and foraging patterns of female Water Pipits Anthus spinoletta were studied in two breeding seasons in an Alpine valley of Switzerland. Decreased temperature reduced the length of periods spent off the nest (inattentive period), while decreased food availability led to a reduction in time spent incubating (attentiveness), shorter periods spent on the nest (attentive period), more frequent inattentive periods and higher foraging effort, measured as the product of frequency of inattentive periods and twice the flight distance to foraging sites. The negative relation between food availability and foraging effort resulted from more frequent foraging bouts and longer flight distances under poor food conditions. Feeding of the incubating female by the male did not affect foraging effort and attentiveness but did change the temporal pattern of inattentive periods from a few long to several short inattentive periods.     

Selection of foraging habitat and nestling diet by Meadow Pipits Anthus pratensis breeding on intensively grazed moorland

Capsule Foraging sites with low vegetation height and density, but with high arthropod biomass, are selected.

Aims To test the hypothesis that on intensively grazed moorland, breeding Meadow Pipits forage for nestling food where arthropod prey are most readily available, and therefore that foraging site choice is a function of prey abundance and vegetation structure.

Methods Observations of adults provisioning nestlings were made from hides positioned close to 19 nests within grazed, 3.3-hectare experimental plots at Glen Finglas, Scotland. Vegetation height and density and arthropod abundance from mapped foraging sites were compared with control sites. Prey items fed to nestlings were quantified and compared with their relative abundance.

Results Meadow Pipits selected foraging sites with significantly lower vegetation height and density, but with significantly higher arthropod biomass. Our data suggest that within foraging sites, Meadow Pipits select particular prey types to provision nestlings, in particular, Lepidoptera larvae, adult Tipulidae and Arachnida.

Conclusions In intensively grazed upland systems, it appears that Meadow Pipits select foraging sites that optimize total food abundance and accessibility. In order to understand how anticipated changes to livestock farming in Europe will affect grassland birds, we recommend that future studies should investigate the foraging and vigilance behaviour, diet composition and breeding success of a variety of bird species provisioning nestlings under a range of livestock management scenarios.     

Proficient incubation by inexperienced Savannah Sparrows Passerculus sandwichensis

We compared the incubation behaviour of 1-year-old female Savannah Sparrows Passerculus sandwichensis nesting for the first time with that of older females that had nested in previous years on Kent Island, New Brunswick, Canada. Using temperature probes inserted into 32 nests, we determined the length and variability of incubation shifts and recesses over 99 nest-days. At 14 of the nests, known-age females were matched, each pair consisting of an inexperienced yearling and an experienced older female, and nest temperatures were measured simultaneously. In addition, we quantified the duration of night-time incubation and the mean length and variation of more than 1350 incubation shifts and recesses as a function of female age, weather, time of day and date. In all respects, yearling and older females had equivalent incubation behaviour. The similarity between yearlings and older females suggests that fundamental aspects of incubation behaviour may be largely innate and unaffected by prior reproductive experience or other age-related variables.     

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.