The demography of Yellow Wagtails Motacilla flava on abandoned fields in northern European Russia

Capsule Apparent survival rates of Yellow Wagtails breeding in abandoned fields in Russia are determined by previous breeding success.

Aims To examine apparent survival and its link to previous breeding success in Yellow Wagtails breeding in abandoned fields in the Vologda region, northern European Russia.

Methods We ringed and measured apparent survival of Yellow Wagtails at two abandoned agricultural sites over eight years (2005–2012). We modelled the impact of age, nest stage, and time of season on daily nest survival rates.

Results Predation was the main cause of nest failure. Nest daily survival rate was highest at the beginning of the breeding season. Overall nest survival probability was 0.40?±?0.02. Adult apparent survival after successful breeding was 0.42?±?0.06 and after unsuccessful breeding this was 0.13?±?0.06.

Conclusion Reproductive success can be regarded as the crucial demographic parameter of the local Yellow Wagtail population in northern European Russia. Apparent survival after successful breeding is significantly higher than after unsuccessful breeding, because unsuccessful breeders probably move to new breeding sites the following year. High adult survival may be particularly important to Yellow Wagtail population dynamics in the study region, because second breeding attempts are apparently unusual.     

Breeding biology of two wagtail subspecies on Ulleung Island,Korea: Amur Wagtails,Motacilla alba leucopsis and Black-backed Wagtails,M. a. lugens

There is much controversy over the species and subspecies status of the white wagtail complex, which is further compounded by interbreeding between two subspecies, the Amur Wagtail (Motacilla alba leucopsis) and the Black-backed Wagtail (M. a. lugens). This study presents preliminary information on the breeding biology of both subspecies on Ulleung Island, Korea, over two breeding seasons (2012–2013). Mixed pairs of the two subspecies were common on this island, with almost 50% of all pairs being heterotypic or intermediate pairs; however, assortative mating was still present. Females of both subspecies were more likely to be paired with Amur wagtail males, whereas intermediate females were more likely to be paired with Black-backed Wagtail males. Clutch size, egg size and mass, and reproductive parameters (such as hatching success and nest success) did not significantly differ from each other. However, the mean values were low in intermediate pairs. Our results indicate no reproductive barrier between the two subspecies, but that some post-isolating mechanisms are still in progress.     

Habitat associations of Yellow Wagtails Motacilla flava flavissima on lowland wet grassland

In common with many other previously widespread British birds, Yellow Wagtail Motacilla flava flavissima populations have declined substantially in the UK in recent decades. Recent national data suggest particular problems in grassland. We investigated how habitat management in a grassland area of East Anglia, England, influenced the habitat selection of this species. Breeding territories were associated with fields previously subject to prolonged winter floods and which contained shallow-edged ponds or wet ditches during summer. Territories were also associated with fields with short, sparse swards and high proportions of bare earth within the sward, and these features were themselves associated with previous winter flooding. However, nests were associated with taller swards than were random points within the same field, suggesting that Yellow Wagtails would benefit from within-field heterogeneity of sward height to provide both nesting and foraging habitat. We discuss how grazing, cutting and water-level management regimes could be used to promote optimal sward structure for Yellow Wagtails.     

Close to the edge: predation risks for two declining farmland passerines

Data on the breeding success of two crop-nesting passerines, Skylark Alauda arvensis and Yellow Wagtail Motacilla flava , were collected in relation to linear features within and surrounding arable crops. Both species were found to experience high rates of nest predation with increased proximity to field boundaries, although the exact nature of the relationship differed with species and, in the case of Skylark, with boundary type. Most nest losses were attributable to predation. During 2006 video cameras deployed on Skylark nests showed that all recorded predation was by mammals of various species, and that these were most active in or around grass margins. The results suggest that further research is needed into ways of minimizing negative impacts of predation on Skylarks. Possible solutions discussed include concentrating Skylark Plots in the field centres away from grass margins and promoting Skylark Plots in fields without grass margins in future agri-environmental schemes.     

Delayed egg‐laying and shortened incubation duration of Arctic‐breeding shorebirds coincide with climate cooling

Biological impacts of climate change are exemplified by shifts in phenology. As the timing of breeding advances, the within‐season relationships between timing of breeding and reproductive traits may change and cause long‐term changes in the population mean value of reproductive traits. We investigated long‐term changes in the timing of breeding and within‐season patterns of clutch size, egg volume, incubation duration, and daily nest survival of three shorebird species between two decades. Based on previously known within‐season patterns and assuming a warming trend, we hypothesized that the timing of clutch initiation would advance between decades and would be coupled with increases in mean clutch size, egg volume, and daily nest survival rate. We monitored 1,378 nests of western sandpipers, semipalmated sandpipers, and red‐necked phalaropes at a subarctic site during 1993–1996 and 2010–2014. Sandpipers have biparental incubation, whereas phalaropes have uniparental incubation. We found an unexpected long‐term cooling trend during the early part of the breeding season. Three species delayed clutch initiation by 5 days in the 2010s relative to the 1990s. Clutch size and daily nest survival showed strong within‐season declines in sandpipers, but not in phalaropes. Egg volume showed strong within‐season declines in one species of sandpiper, but increased in phalaropes. Despite the within‐season patterns in traits and shifts in phenology, clutch size, egg volume, and daily nest survival were similar between decades. In contrast, incubation duration did not show within‐season variation, but decreased by 2 days in sandpipers and increased by 2 days in phalaropes. Shorebirds demonstrated variable breeding phenology and incubation duration in relation to climate cooling, but little change in nonphenological components of traits. Our results indicate that the breeding phenology of shorebirds is closely associated with the temperature conditions on breeding ground, the effects of which can vary among reproductive traits and among sympatric species.     

Breeding biology of White‐rumped Tanagers in central Brazil

ABSTRACT White‐rumped Tanagers (Cypsnagra hirundinacea) are widely distributed in northern Brazil, Bolivia, and Paraguay, and are classified as vulnerable in the state of Paraná and as endangered in the state of São Paulo, Brazil. Little is currently known about their breeding biology. We studied the breeding behavior of White‐rumped Tanagers in the Cerrado (Neotropical savanna) in central Brazil from 2002 to 2007. The breeding period extended from mid‐August to mid‐December. Nests were cup‐shaped and located mainly in trees of the genus Kielmeyera at a mean height of 3.7 ± 0.3 m (SE). Clutch sizes varied from one to three eggs and the incubation period lasted an average of 16.0 ± 0.3 d. Incubation was by females only and started with the laying of the first egg. Mean nest attentiveness (percent time on nests by females) was 64 ± 0.08%. Nestlings were fed by males, females, and, when present, helpers. The mean rate of food delivery rate to nests was 5.2 ± 0.4 items/h, with rates similar for males (mean = 2.7 ± 0.3 items/h) and females (mean = 2.4 ± 0.3 items/h). The mean duration of the nestling period was 12.1 ± 0.5 d. Compared to many temperate species of tanagers, White‐rumped Tanagers in our study had relatively small clutches, low nest attentiveness, and long incubation periods. As with other tropical species, such characteristics might be due to food limitation or high rates of nest predation.     

Life‐history tradeoffs revealed by seasonal declines in reproductive traits of Arctic‐breeding shorebirds

Seasonal declines in breeding performance are widespread in wild animals, resulting from temporal changes in environmental conditions or from individual variation. Seasonal declines might drive selection for early breeding, with implications for other stages of the annual cycle. Alternatively, selection on the phenology of nonbreeding stages could constrain timing of the breeding season and lead to seasonal changes in reproductive performance. We studied 25 taxa of migratory shorebirds (including five subspecies) at 16 arctic sites in Russia, Alaska, and Canada. We investigated seasonal changes in four reproductive traits, and developed a novel Bayesian risk‐partitioning model of daily nest survival to examine seasonal trends in two causes of nest failure. We found strong seasonal declines in reproductive traits for a subset of species. The probability of laying a full four‐egg clutch declined by 8–78% in 12 of 25 taxa tested, daily nest survival rates declined by 1–12% in eight of 22 taxa, incubation duration declined by 2.0–2.5% in two of seven taxa, and mean egg volume declined by 5% in one of 15 taxa. Temporal changes were not fully explained by individual variation. Across all species, the proportion of failed nests that were depredated declined over the season from 0.98 to 0.60, while the proportion abandoned increased from 0.01 to 0.35 and drove the seasonal declines in nest survival. An increase in abandonment of late nests is consistent with a life‐history tradeoff whereby either adult mortality increased or adults deserted the breeding attempt to maximize adult survival. In turn, seasonal declines in clutch size and incubation duration might be adaptive to hasten hatching of later nests. In other species of shorebirds, we found no seasonal patterns in breeding performance, suggesting that some species are not subject to selective pressure for early breeding.     

Breeding ecology of Yellow Wagtails Motacilla flava in an arable landscape dominated by autumn-sown crops

Capsule Yellow Wagtails successfully raised two consecutive broods in landscapes dominated by autumn-sown crops and did not require spring crops or fallow plots for later nesting.

Aims To assess whether arable landscapes dominated by winter cropping provide habitats that allow Yellow Wagtails to raise two successful broods. To assess the utility of spring cultivated agri-environment fallow plots as a nesting and foraging habitat for Yellow Wagtails.

Methods Nesting success and foraging behaviour of Yellow Wagtails was monitored on lowland arable farmland dominated by winter cropping during two successive breeding seasons.

Results Yellow Wagtails successfully raised first and second broods mainly in winter cereals, with later nests being more successful. Some nests were initiated in bean fields where egg-stage failure rates were high, probably as a consequence of depredation. Fallow plots were not used for nesting but, along with other areas of sparse vegetation, were regularly used for foraging.

Conclusions Yellow Wagtails breeding at relatively low densities achieved high rates of reproductive success in a landscape dominated by winter cereals and with few spring-sown crops. This study suggests that spring-sown crops may not be necessary for Yellow Wagtails to rear two successful broods each summer within arable landscapes.     

Yellow Wagtail Motacilla flava migration from West Africa to Europe: pointers towards a conservation strategy for migrants on passage

The biology of one passerine migrant, the Yellow Wagtail Motacilla flava, is examined in order to identify factors which need to be considered when attempting to conserve migrants on passage. The distribution of Yellow Wagtails in West Africa, prior to northward (spring) migration, is affected by food supplies and by different racial and sexual responses to environmental factors. Consequently, each breeding population relies on a wide range of sites, but those occupied towards the end of the dry season and ones used as stepping-off points for migration may be particularly vital.
Energetic considerations point towards a non-stop trans-Saharan flight being used rather than a series of short flights with resting stops in the desert. However, adverse conditions during migration could make stop-overs unavoidable. The most direct routes between wintering and breeding areas are preferred, and the initial desert crossing is accomplished at a faster pace than later stages of the journey.
Yellow Wagtails emigrate from West Africa in a sequence related to the onset of spring on their breeding sites, rather than in response to rainfall in Africa: moult, fattening and emigration are probably endogenously controlled. However, competition from African resident birds may also be an important factor affecting the timing of migration.
Races breeding in southern Europe are most likely to be adversely affected by degradation of the Sahel. Empirical evidence suggests that conditions on the wintering grounds are more likely to regulate population size than conditions experienced on migration, but more detailed studies are needed in Africa before sound conservation strategies can be designed.     

THE BIRDS OF LANGEBAAN LAGOON

Data are presented on breeding success of Red Bishops (Euplectes orix) collected over four breeding seasons at a colony in the Addo Elephant National Park, Eastern Cape, South Africa. Overall hatching and fledging success were 53.8% and 26.0% of all eggs laid, respectively, and the overall mean number of fledglings per breeding attempt was 0.77. Hatching and fledging success varied significantly among seasons, with both clutch and brood losses due to predation being the main reason for the observed differences. Hatching success also differed significantly among clutch sizes, being highest for four-egg clutches (63.2%), intermediate for three-egg clutches (55.5%) and lowest for two-egg clutches and five-egg clutches (33.2% and 34.3%, respectively). However, fledging success was not significantly different among clutch sizes. The mean number of fledglings per breeding attempt was 0.44 for two-egg clutches, 0.80 for three-egg clutches, 1.10 for four-egg clutches, and 0.57 for five-egg clutches. The height of accepted nests (i.e.nests in which at least one egg was laid) was significantly lower than the height of nests not accepted. In addition, accepted nests in which eggs hatched and young fledged were significantly lower than accepted nests in which no eggs hatched and no young fledged. These overall effects of nest height on nest acceptance and hatching and fledging success were, however, due only to nests built above water, since no such effects were found when nests built above ground (i.e.on dry land) were analysed separately. I detected no effect of nest coverage on the probability of a nest being accepted, nor was there any effect of nest coverage on hatching or fledging success. Nests above water were significantly more likely to be accepted than nests above ground; however, hatching and fledging success of nests that were accepted did not differ significantly between nests built above water and those built above ground.     

Nesting ecology of solitary‐nesting Amur Falcons (Falco amurensis) in central Mongolia

Amur Falcons (Falco amurensis) are a migratory species that face a variety of threats across their range, but little is known about their breeding ecology. These falcons breed in forest habitats in Eastern and Central Asia using nests constructed by corvids, including Eurasian Magpies (Pica pica). We monitored nests of 21 pairs of Amur Falcons at Hustai National Park in central Mongolia in 2017. Our objectives were to describe their basic nesting ecology, estimate nest survival by modeling the daily survival rate (DSR), examine nest selection by modeling it as a function of nest and site covariates, and use a spatial simulation to test hypotheses concerning intra‐ and interspecific avoidance. Clutch sizes averaged 4.1 eggs (N = 21 nests), and incubation and nestling periods averaged 25.7 and 26.1 d, respectively. The daily survival rate was 0.98, with young in 12 nests surviving to fledging. Nest structures were more likely to be selected as percent cover of nest bowls increased, usually in the form of a dome of sticks with multiple side entrances. Closed nests likely provide increased protection from predators. In contrast to congeneric Red‐footed Falcons (F. vespertinus) that nest in large colonies, Amur Falcons nested no farther from or closer to nests of either conspecifics or congeners than expected by chance. One factor likely contributing to this difference is that Red‐footed Falcons often use the nests of colonial‐nesting Rooks (Corvus frugilegus), whereas Amur Falcons typically use the nests of non‐colonial Eurasian Magpies. The ongoing loss of deciduous trees like white birch (Betula platyphylla) across the breeding range of Amur Falcons, probably due to climate change and increased grazing pressure, is likely to reduce the availability of nesting habitat for Eurasian Magpies which, in turn, will likely reduce availability of nests for Amur Falcons and other small falcons.     

Breeding biology and social behaviour of Magellanic Woodpeckers (<Emphasis Type="Italic">Campephilus magellanicus</Emphasis>) in Argentine Patagonia

The Magellanic Woodpecker (Campephilus magellanicus) is a poorly known species endemic of the Austral Temperate Forests of South America, where it is a potential keystone habitat modifier. Here, I summarize data on the social and breeding biology of this woodpecker, based on 22 active nests located from 1998–2002 in forests from northwestern Argentine Patagonia. Woodpeckers normally traveled in pairs or family parties. In late Austral winter, one to three cavities were selected for completion at each territory. Breeding occurred between mid- to late spring and early to mid-summer, and took about 65 days. Monogamous parents shared duties in nest excavation, incubation and young rearing. Egg length (±SD) measured 34.13±0.79 mm and egg breadth 23.91±0.67 mm, and incubation took roughly 20 days. Nestlings were altricial and remained at the nest for about 45 days. Clutch size was one, occasionally two eggs, and one nestling was produced at all successful nests. Young remained with their family group for up to 2 years or more, and were fed by adults, who normally bred every second year. Nest re-use, nest predation and helpers at the nest were not recorded. Holes were placed (±SD) 8.84±3.71 m high and were 32.3±5.32 cm deep. Entrances (±SD) were 8.92±0.46 cm wide and 15.59±2.54 cm high and mostly oval in shape. Peculiarities of the breeding biology and social behaviour of this species are discussed in the light of patterns common to picids, especially Campephilus spp.     

Habitat-specific clutch size and cost of incubation in eiders reconsidered

The energetic incubation constraint hypothesis (EICH) for clutch size states that birds breeding in poor habitat may free up resources for future reproduction by laying a smaller clutch. The eider (Somateria mollissima) is considered a candidate for supporting this hypothesis. Clutch size is smaller in exposed nests, presumably because of faster heat loss and higher incubation cost, and, hence, smaller optimal clutch size. However, an alternative explanation is partial predation: the first egg(s) are left unattended and vulnerable to predation, which may disproportionately affect exposed nests, so clutch size may be underestimated. We experimentally investigated whether predation on first-laid eggs in eiders depends on nest cover. We then re-evaluated how nesting habitat affects clutch size and incubation costs based on long-term data, accounting for confounding effects between habitat and individual quality. We also experimentally assessed adult survival costs of nesting in sheltered nests. The risk of egg predation in experimental nests decreased with cover. Confounding between individual and habitat quality is unlikely, as clutch size was also smaller in open nests within individuals, and early and late breeders had similar nest cover characteristics. A trade-off between clutch and female safety may explain nest cover variation, as the risk of female capture by us, mimicking predation on adults, increased with nest cover. Nest habitat had no effect on female hatching weight or weight loss, while lower temperature during incubation had an unanticipated positive relationship with hatching weight. There were no indications of elevated costs of incubating larger clutches, while clutch size and colony size were positively correlated, a pattern not predicted by the ‘energetic incubation constraint’ hypothesis. Differential partial clutch predation thus offers the more parsimonious explanation for clutch size variation among habitats in eiders, highlighting the need for caution when analysing fecundity and associated life-history parameters when habitat-specific rates of clutch predation occur.     

An inexpensive method for remotely monitoring nest activity

ABSTRACT.   In studies of avian nest success, investigators often face the difficult task of periodically checking nest status while at the same time limiting observer influence on nest survival. Remotely monitoring nests using temperature data loggers is one method that allows for continuous data capture regarding nest status (i.e., active vs. inactive) without the negative effects associated with repeated nest checks. We used small temperature data loggers (Thermochron iButtons) to remotely monitor nests of Long-billed Curlews ( Numenius americanus ) in northeastern Nevada. Data loggers programmed to record temperature at 10-min and 20-min intervals were placed in curlew nests. Data loggers were set to collect data throughout the nesting cycle to determine onset of incubation and timing of nest failure. On average, Long-billed Curlews began incubating approximately 3 d after the first egg was laid and onset of incubation coincided with the laying of the third egg. iButtons allowed us to determine when incubation was terminated in 17 of 23 unsuccessful Long-billed Curlew nests, including 13 of 17 depredated nests. The presence of iButtons in Long-billed Curlew nests did not affect daily survival rate, egg hatchability or rate of nest abandonment. iButtons are an efficient and practical means for remotely monitoring nests of large egg-laying birds, such as the Long-billed Curlew.     

Annual and seasonal reproductive trends in the Lesser Spotted Woodpecker Dendrocopos minor

Annual and seasonal variation in reproductive timing and performance were studied in a population of the Lesser Spotted Woodpecker Dendrocopos minor over 10 years in southern Sweden. The median laying date of the first egg varied by up to 17 days between years, being generally larger than the variation of laying dates within years. Neither clutch size, brood size in successful nests, fledging success in successful nests nor mean nestling weight differed significantly between years. There was no trend for mean clutch size to vary between early and late years. In spite of a more than threefold variation in population size, no reproductive variable demonstrated an apparent density-dependence. Within the season, clutch size declined steeply with increasing clutch initiation date, whereas fledging success and nesting success did not, leading to a trend in brood size almost identical to the trend in clutch size. The survival prospects of fledged young declined with increasing clutch initiation date, and it is argued that the clutch size laid is a strategic adjustment to laying date. Out of 124 breeding attempts, 34% did not produce fledged young. In 9% of the breeding attempts, pairs laid no eggs. At least 20% of the breeding attempts failed after egg-laying. The most common cause of breeding failure was loss of the breeding partner followed by nest abandonment (40% of the failures). Only 16–28% of the failures were due to predation on the nest. Most complete failures, and also partial losses from nests, occurred at the early breeding stages. It is argued that the early nestling phase may be a critical stage, which the woodpeckers adjust to coincide with the seasonal food peak, explaining the strikingly late breeding season compared with other non-migrant species.     

Sprague's pipit breeding biology and reproductive success in planted and native grasslands

Much of the native grasslands in agricultural regions have been converted to cropland or tilled and seeded with non‐native grasses for livestock production. Several grassland songbird species occupy planted grasslands, but occupancy or density may not be a reliable indicator of habitat quality. I studied the breeding biology of Sprague's pipit Anthus spragueii from 2004 to 2008 in Saskatchewan, Canada. My objective was to determine the extent to which the breeding biology, density and reproductive success of pipits varied in planted and native grasslands. Peak clutch initiation occurred in mid‐ to late‐May in planted and native grassland. Peak pipit density also occurred in May, but density drastically declined over the breeding season in planted grassland. Clutch size varied among years and declined over the breeding season, but was similar in planted (4.7  0.1 SE) and native grasslands (4.5  0.1 SE). Daily nest survival rates varied with age of the nest and date, but the relationships differed in the two habitats and was likely a result of lower nestling survival in planted grassland compared to native grassland. The number of young fledged per nest increased as the season progressed and tended to be greater in native (1.2  0.1 SE) than planted (0.9  0.2 SE) grasslands. Seasonal productivity was much greater in native grassland. Only three nests were initiated after May in planted grassland and all were unsuccessful, whereas pipit young fledged at higher rates from nests initiated in native grassland in June and July than planted grassland nests initiated in May. The number of fledged young from successful nests did not vary strongly with habitat, date or year. This research indicates that planted grasslands attract pipits at the beginning of the breeding season, but habitat suitability and reproductive success substantially declines as the breeding season progresses compared to that found in native grassland.     

Function of egg punctures by Shiny Cowbirds in parasitized and nonparasitized Creamy‐bellied Thrush nests

ABSTRACT Avian brood parasites usually remove or puncture host eggs. Several hypotheses have been proposed to explain the function of these behaviors. Removing or puncturing host eggs may enhance the efficiency of incubation of cowbird eggs (incubation‐efficiency hypothesis) or reduce competition for food between cowbird and host chicks in parasitized nests (competition‐reduction hypothesis) and, in nonparasitized nests, may force hosts to renest and provide cowbirds with new opportunities for parasitism when nests are too advanced to be parasitized (nest‐predation hypothesis). Puncturing eggs may also allow cowbirds to assess the development of host eggs and use this information to decide whether to parasitize a nest (test‐incubation hypothesis). From 1999 to 2002, we tested these hypotheses using a population of Creamy‐bellied Thrushes (Turdus amaurochalinus) in Argentina that was heavily parasitized by Shiny Cowbirds (Molothrus bonariensis). We found that 56 of 94 Creamy‐bellied Thrush nests (60%) found during nest building or egg laying were parasitized by Shiny Cowbirds, and the mean number of cowbird eggs per parasitized nest was 1.6 ± 0.1 (N= 54 nests). At least one thrush egg was punctured in 71% (40/56) of parasitized nests, and 42% (16/38) of nonparasitized nests. We found that cowbird hatching success did not differ among nests where zero, one, or two thrush eggs were punctured and that the proportion of egg punctures associated with parasitism decreased as incubation progressed. Thus, our results do not support the incubation‐efficiency, nest‐predation, or test‐incubation hypotheses. However, the survival of cowbird chicks in our study was negatively associated with the number of thrush chicks. Thus, our results support the competition‐reduction hypothesis, with Shiny Cowbirds reducing competition between their young and host chicks by puncturing host eggs in parasitized nests.     

Intraspecific nest parasitism in the Spotless Starling Sturnus unicolor

Intraspecific nest parasitism in two colonies of Spotless Starling Sturnus unicolor breeding in nestboxes was studied in central Spain from 1991 to 1994. Nests were monitored regularly and three criteria were used to detect nest parasitism: the appearance of more than one egg per day during the laying period of the host; the appearance of an egg after the start of incubation; eggs with unusual shape or pigmentation. The proportion of parasitized nests in first clutches (37%) was twice that of intermediate (19%) or second (20%) clutches in colony B, whereas parasitism occurred in first (35%) and intermediate (12%) but not in second clutches in colony A. Most clutches (52–70%) were parasitized during the host's laying period and received one parasitic egg. In 10% of the parasitized clutches in colony B, one of the host's eggs disappeared on the day the parasitic egg was added, suggesting that the parasitic female removed this egg. Although parasitism increased clutch size significantly, it led to a decrease in host breeding success, mainly through the removal of eggs and the loss of host nestlings and the survival of parasitic chicks. Observations suggested that parasitic females were young individuals without their own nests and/or those whose breeding attempt had been disrupted while laying in their own nest.     

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。     

Week-end bias at observatories

Capsule Although subject to human disturbance Turtle Doves do nest successfully in these olive and orange orchards.

Aim To investigate the breeding ecology of Turtle Doves in a man‐made agricultural habitat in central Morocco.

Methods Turtle Dove nests were monitored in orange and olive orchards over three years (2006, 2007 and 2008). Nest abundance, nest location, egg‐laying chronology, clutch size, nest survival rates and breeding success were determined and compared between orchard types.

Results The Moroccan population of Turtle Doves start breeding earlier than European populations. Clutch size, nest survival rates and breeding success were similar in orange and olive orchards. Nest location differed between orange and olive trees. Nest densities were 16 nests/ha in olive orchards and 45 nests/ha in orange orchards. Nest success rate averaged 48%. Daily nest survival rates did not vary according to orchard types, year and date. In the two orchards, no nest position variables were significant predictors of nesting success.

Conclusion Although highly frequented by people, fruit orchards seem to be suitable breeding habitats for Turtle Doves in this region.