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the offspring. 59 of 99 reduced broods were males, while 34 of 81 unmodified broods male. Although sometimes said to only fed young at night, the mother can also parse out tiny bits of food by day to their nestlings. The young are fed small bits of meat for about 12 days, at which point the young open their eyes and begin to more actively beg. Also around 12 days, the nestlings produce their first pellets, though they are often of a rather liquid consistency.< Older nestlings beg with quivering wings and intense high-pitched food begging calls. Female only regularly hunts again after brooding period (usually a little after the young are 2 weeks old). The male tends not to enter the nest to make food delivery, often the female receives it nearby on a branch of the tree or at the entrance of the nest hole, later when the nestlings are large, the male often will silently deposit the prey directly into the nest without landing. When the young are 21–25 days old, young begin to spend much time around the entrance of nest hole, and may begin to emerge 3–5 days later. It was found in warmer conditions, that the owlets born to rufous morph mothers requires less oxygen consumption and may have experienced less stress. Evidently the oldest is usually the first to leave hole. After leaving the nest and becoming "branchers", the young owls often clamor around using both the feet and the beak, and often land on the forest floor, from where they tend to flutter and climb into bushes, trying to reach higher parts of the trees (and should not be handled if found on the ground as such). Finally, at 29–37 days, with an average of 32.1 days in
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59.5% failed in urban plots and 51.3% in suburban areas, with 18.5% and 23.4% in urban and suburban zones producing 1 fledgling, 12% and 18% producing 2, 8% and 7.2% producing 3 and 2% in the urban area producing 4. In Roman areas, the breeding rates are generally quite low but are fairly stable annually, due to warmer average ambient temperature and less local trophic competition. The total breeding success in Roman pairs was 43.5% in the city (also 0.83 fledglings per pair and 1.86 per successful pairs) and 51% in suburbs (also 0.82 fledglings per pair, 1.63 per successful pair). Of 256 Belgian eggs, 24% did not hatch, 10% of those were deserted, 51% were addled and 39% were deserted or destroyed by the female when food supply was low. In the
Belgian data, of 195 young hatched, 94% fledged and 6% died in nest as a result of starvation, with an average number of fledglings 2.06, varying from 0 to 3.25 on average in different years based on vole numbers. In southern France, brood size for all pairs was 2.2 while for successful pair it was 3.2 (range 2–4.3 per pair). In the French study, cannibalism was reportedly surprisingly often to be committed by mother or siblings. 73.7% of the studied French broods produced fledglings. Of 357 pairs in the woodlands around
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but while still dependent and were quite likely preyed upon while the only 4 remaining lost radio contact after leaving parent's range at 58–178 days after fledging. Of 13 certain to have died, 6 were due to starvation, 3 were due to predation by goshawks, one by an infected eye injury, while the rest of uncertain cause. Mortality rates can be even higher elsewhere such as an average of about 92% in
Scotland and about 61% in Norway for juveniles before they disperse. Meanwhile recorded average mortality rates in the 1st year of radio-tagged tawny owl lives were recorded as the following averages: Sweden at 71.7%, Switzerland at 49.4%, England at 52.6%, west Germany at 48% and Belgium at 58%. Radiotagging studies showed average mortality for Swedish 2nd year owls was 44.3%, 24.5% at this point for Swiss owls and 22.2% for English ones while in the third year the Swedish one's mortality was estimated to average 47.6% and English ones at 31.8%. The survival rate average over two decades was unexpectedly somewhat high in Finland in about 20,000 owls, where it was 33% in the 1st year, 64% in 2nd year, 73% in subsequent years. In England, it was estimated that there was 6–11 times lower survival rate for tawny owls that were
414:, but take about another two weeks before they can fly strongly. The young post-fledgling owls continue to beg, often following and rarely leaving an area of about 50 m (160 ft) away from their mother. The pre-dispersal young used an area of 5 to 15 ha (12 to 37 acres) in England while, in Scotland, it was only 2.2 to 6.5 ha (5.4 to 16.1 acres). In Denmark, the distance between post-fledging siblings ranged from 11 to 0.6 m (36.1 to 2.0 ft) during day and 32 to 6 m (105 to 20 ft) by night, meaning that they are associative with one another at this stage, and they would spend 20–80% of nighttime hours food begging, up to 82% in poor food years. At around 1 to 3 months (sooner in Denmark, later in England on average), the young tawny owls begin to hunt for themselves. At the age of 2 to 3 months the young owls can be evicted by their parents, although often appear to disperse independently. However, on average of 72 radio-tagged juveniles in Denmark after the young owls would stop begging for food at 90–123 days of age, they would typically roost within their parents territories for another 18 days without incident. In the Danish
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Berlin metropolitan, nesting success averaged 2.1 and 2.8 per successful nest, but could vary 2.7 to 3.2 on average in low and high vole years. In eastern
Bohemia, an average 2.6 young fledged per successful pair, but no determinable difference in productivity was noted during good and poor prey years. Breeding success varied in Finland based on vole numbers, from 2.4–2.7 in poor years to 3.4–3.5 in good years, but only a slight variation was recorded in clutch size and young hatched. Finland has shown a sharp increase overall in tawny owls in the recent three decades was from 422 to 1710 active territories found, from 198 to 1566 nests found and from 168 to 1341 successful nests found. When vole populations were high, the number of young tawny owls introduced into the population of Finland was ten times higher than in low years. It was found in Denmark that a control group of 32 out of 131 radio-tagged young that were supplementally fed by researchers were more vulnerable to predation (36% of these died, mostly due to mammals like foxes around fledging age) but also earlier nests were vulnerable as well (more so to other birds of prey).
331:). Sometimes when the mother feeds their young, separated feathers are sometimes doled out and consumed by them. In France, 4–19 prey deliveries by the male were recorded per night, or 2.5–3 prey per chick nightly. In Belgium, from as little as 0 to 22 prey items were recorded to be delivered per night, on average 3.7 (range 2.3–5.1) prey per chick nightly. Up to 21% of prey deliveries were done in daylight in Wytham whereas in the Netherlands only 2% were during daytime. In one British nest, with three owlets (the oldest being 15–25 days old) each chick received about 88 g (3.1 oz) of food per night while later near fledging, each would get 124 to 141 g (4.4 to 5.0 oz) per night. In an experiment study, broods were both increased and decreased to see if males differed their food deliveries, it was found that the males did change their food delivers as a result of brood increase or decrease, with the decreased broods being fed well while the increased broods were food stressed and showed particular signs of declining condition of the brooding female as she had less food for herself.
435:, 1992–2000, the age of females appeared to effect the number of eggs and hatching success, while the age of the male effected the number of fledglings, with 39 pairs studied, with 98 females and 85 males produced in network of 180 nest boxes. Again older males and females (i.e. 5 to 9) were seemingly more productive overall. Hungarian data shows lower overall number of young during years with harsh, snowy winters but due to the low number of young, the successful raised young were stronger and in better condition on average once fully grown than the young owls in years with many offspring. The breeding success overall in Lithuania has steadily increased, with a survival rate reached of 72% for females. The area of
418:, 41 radio-tracked broods were dependent after fledging for a mean of 71 days (with a range of 56–84). 5 of 12 radiotagged juveniles survived dispersal in a different study from Denmark, independence was gained at an average 77.3 days and single day movements recorded of up to 4 km (2.5 mi). 22 radiotagged young tawny owls in England were tracked post-dispersal relative to vole concentrations, though there was no evidence that there were consistently able to access the peak vole areas. 27.4% of area selection was found to be likely correlated to vole access. The age at first breeding may be early as one year, but is more commonly 2–3 years old and rarely not until 4 years old.
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males. Later into the nesting period, the female may begin showing more aggressive reactions to disturbance or threats. Older females were found in a study show a more aggressive defense as well as those with larger broods and earlier nestings, however non-aggressive females were found to have more future reproductive years on average than aggressive ones. Rufous morph females were more vigorous in nest defense than other morphs in a study from
Switzerland. At the first detection of an intruder, the female may let out muffled hoots initially. Attacks only tend to occur somewhat regularly in developed areas, especially city parks, where repeated intrusions occur and perhaps resulting
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reduction from 1992 to 1998. In this area, due probably to the exotic conifer dominated forest, owls were quite dependent on field vole numbers in the openings, and could vary from twentyfold from low to high years, with 70% of the variance of productivity could be correlated to the habitat types available and show the importance of habitat heterogeneity. In peak years at
Kielder, of 197 attempts, 6.9% failed to breed and 28.3% successfully bred, in the increase years, of 44 attempts, 10.2% failed to breed and nesting successful was 76.2% and in the decrease years, of 62 attempts, 12.5% failed to breed and nesting success average was 69%.
309:, 2.95 in Belgium 3.29 in central Europe, 3.3 in both Switzerland and the Netherlands, 3.65 in Denmark, 3.64–3.81 in Finland and 4.04 in Sweden. While in Bohemia, the clutch size varied remarkably little by year, in western Switzerland it could go from 2.52 to 3.63 in different years and Finnish data indicates it can vary from 3.1 to 4.2 in low and peak vole years. Therefore, clutch size may be more variable in more cool climatic zones but, on the other hand, the average size of the clutches averages larger in these colder areas. Although clutch sizes average smaller in
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47.6 mm × 39.2 mm (1.87 in × 1.54 in) in central Europe, 46.6 mm × 38.5 mm (1.83 in × 1.52 in) in Sweden (Makatsch 1976) and 47.5 mm × 39.2 mm (1.87 in × 1.54 in) in Russia. The range may be from 42 to 50 mm (1.7 to 2.0 in) in height by 36 to 41 mm (1.4 to 1.6 in) in diameter (sample size 100). The average weight of eggs can vary from 31.3 to 40 g (1.10 to 1.41 oz).
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mice, due to the owl's ability to exploit alternate prey in poor rodent years. In
Scotland, perhaps with less diverse prey available in the more northern clime, the trends of tawny owls were more sharp: 2.6 fledglings were produced in good vole years, 1.65 average in declining years and 0.2 in poor vole years over a 7 year period. Scottish data showed nestling mortality was higher in poor vole years, at about 31% vs 14% in good vole years, with no sex bias. During low prey years in
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fights. Territories have been known to have been maintained by single tawnys for up to 10 years in Russia and 13 years in Berlin. Of 34 males in Wytham, only one male moved off of territory, due to being disturbed by humans. It appears to be largely up to the male to select territorial boundaries. Despite the aforementioned territorial behaviour, active nests of two separate pairs at as close as 100 m (330 ft), in the
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owl's reputation as a highly aggressive bird when encroached upon, the parents are usually retiring even when the area of the nest is broached. Passive measures are usually taken first in parental nest defense. The mother owls are often tight sitters, one female sat motionless even as she was physically turned over, while another sat tight but flushed eventually after several human intrusions. Sometimes parents engage in
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339:, with the female's age being the most significant factors that could be determined. Furthermore, it was found that male condition was the most important factor for female condition, with older males often in better physical condition. Weather conditions were found to be intrinsic with condition of parents in Finland, and further that larger females could breed earlier and more successfully on average. A study of
305:, Spain of a second successful clutch was produced, with pairs of owlets were recorded in February then another pair of owlets apparently hatched to the same pair was recorded in July of same year. The female typically lays a relatively small clutch of 3–5 eggs, sometimes in extreme case from 2 and very rarely and in the times of food plenty, 7–9. Average clutch sizes were cited as 2.67 in Britain, 2.8 in
28:
140:, with only 12.3% of the 44% of nest boxes actually used by owls for breeding, usually with the owls utilizing boxes that were at least 6 m (20 ft) above the ground. Nest boxes are most successful wherever natural tree cavities are scarce or absent, such as conifer forests, young successional woods and farmlands. Tawny owls may not infrequently nest in an unmodified
47:, have been reported. This species shows very little extrapair parentage. In Switzerland for example, a study of 137 nestings found that only one, or 0.7%, were from a different father than the mate, females cannot generally raise young without male contribution so the pair structure of these highly residential owls insures little instance of
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contact is made, especially if the person turns their back, but even then often veer short of physical contact. Humans are inefficient at fending off sudden physical attacks because of the silent flight of the owls. Tawny owl mothers not infrequently attack threatening animals common in parks such as dogs and cats as well as
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may resume her hunting but the male may continue to a majority of food capture and may even feed the offspring directly. Larger prey items tend to be more often fed to chicks such as medium-sized birds, young rabbits and moles where available, while the parents themselves usually eat small rodents (i.e. in Wytham and
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peaceably allow them in the vicinity. Although moderately hardy during sub-freezing winters, severe winters can be dangerous in areas such as the
Russian part of their range. Mortality in general in the northern limits of the range is probably higher than Ural owl. This species is increasingly affected by
1721:. In In: Duncan, James R.; Johnson, David H.; Nicholls, Thomas H., eds. Biology and conservation of owls of the Northern Hemisphere: 2nd International symposium. Gen. Tech. Rep. NC-190. St. Paul, MN: US Dept. of Agriculture, Forest Service, North Central Forest Experiment Station. 111–118. (Vol. 190).
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levels in differently sized clutches in
Hungary with smaller clutches with lower testosterone levels being male-biased. In this Hungarian study, survival rates were higher in smaller broods than in larger brood. Heavier parents raised all offspring hatched to them, while lighter parents raised 33% of
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in
Hungary determined that experienced parents produced nestlings with more testostrone mainly in correlation with mild weather. In poor weather or inexperienced parents the levels were lower. The testostrone levels in the Hungarian study were found to be lowest in poor weather conditions in the last
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than in mainland Europe, they are more consistently laid there than the clutches of barn owls. Their eggs are pure white, smooth or slightly glossy in texture, and vary little in size. Egg dimensions were found to average 46.7 mm × 39.1 mm (1.84 in × 1.54 in) in
Britain,
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in 2 decades starting 1958, 160 pairs produced 333 fledglings, with an average of 2.08 per successful nest. 13 pairs in the city parks of west Berlin produced 47 fledglings, 3.3 pairs per successful nest, productivity strongly correlated to number of yellow-necked mice available. More broadly in the
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in Italy, out of 326 attempts, 4–28% were successful in different years, with the number fledglings ranged from 0.4–1 overall and 1-1.18 per successful pair and habitats with more rainfall and less arid conditions being more productive. Of 311 breeding attempts studied over a 13 year period in Rome,
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occurs but is slightly less pronounced perhaps than long-eared and barn owls, rarely ranging up to 2–3 days apart. The female broods the owlets closely until 10–15 days, rarely ceasing as early as 7 days. In a Danish study, it was found that 59% of 268 nestlings were male, as opposed to roughly even
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in a selected 51 pairs within Denmark (from a network of 204 nest boxes) were used to measure hormone levels. It was found that testostrone levels were consistently higher in 3 year old birds of both sexes, birds of this age were more productive in all aspects of breeding than younger owls, although
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Tawny owls can live to more than a decade. The oldest recorded in the wild in central Europe was 18 years and 7 months old while the oldest in Sweden recorded was nearly 14 years old. These records were subsequently broken by a female recorded in the wild in Switzerland at an age of 21 years and 11
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and territorial year around. Young birds select territories and look for mates in autumn and tend to be very vocal, especially males. Due to their highly territorial behaviour, young birds frequently struggle to establish a territory unless a nearby adult dies. Males routinely engage in territorial
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causes of mortality are covered later. Of 22 radio-tagged young tawny owls in Kielder, 36.4% (8) owls died 10-106 days after fledgling but while still on parent's ranges, another 22.7% (5) died after leaving parents territory at 40–147 days after fledgling, 22.7% (5) also disappeared after fledged
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Breeding success averages fairly high in this species. A study within oak-hornbeam-birch forest in Hungary on the breeding output of males, 77 males examined from the 1st breeding year until 9 years of age, increase breeding output from 2 to 4 years of age thence peaking at 5–6 in age. However, at
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owls as well. In the earlier part of the nestling period, males sometimes launch defensive attacks but these tend to be relatively mild and no physical contact is often made. In western Switzerland, females were 2.9 times more likely to respond aggressively to artificial nest predator stimuli than
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When they are alarmed or required to act in self-defense near the nest, tawny owls of all ages but especially older nestlings up to fledging age, have been recorded to raise feathers and outstretch wings, to their expand size and possible shield itself, also snapping their bills. Despite the tawny
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alone, starting with the first egg for 28–29 days typically, and is fed by the male. The female also broods the chicks, feeding them strips of meat for about 2 weeks, after which they may start swallowing mice and such whole. She continues to feed them until they leave the nest, at which point she
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being primary). Starvation rates are high in newly independent young if there is no unoccupied territories in the vicinity (at least by 1 bird of their corresponding gender). Mortality averaged about 15% in territorial adults in Wytham. In Finland, Ural owl displaced tawny owls but great grey owl
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produced an average of 0.3 for all territories in fragmented woods and 0.89 for all territories in continuous woods. This study of the English countryside showed that the owl population varied relatively little in proportion to the sharply cyclic nature of the main prey here, field voles and wood
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and irritation. Some individual females and rarely males become routine attackers on humans and may be known as "furies". In at least some cases parks may be closed due to unprovoked tawny owl attacks. The female tends to attack humans from behind and focus on the head and shoulders when physical
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in France, productivity of successful pairs avg 3.2, varying from 2 to 3 to 4 in poor, intermediate and good prey years. In western Switzerland, over the course of 14 years, females produced an average of 5.67 fledglings. On an area of 3,800 ha (9,400 acres) in the Netherlands, 9 successful
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are able to biological predict the vole numbers based on spring feeding access and produce more often the more productive sex, which were females here. Territorial changes in Kielder were associated to habitat and land use changes with 25% more territories recorded from 1981 to 1991 then a 21%
485:, the incidence of which has tripled in the last 70 years, in parallel with increasing global temperatures. An increase of one degree Celsius produces a two- to three-fold increase in the rate of malaria. In 2010, the incidence in British tawny owls was 60%, compared to 2–3% in 1996. Direct
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when attempting to protect their young but less frequently than do long-eared owls. There is much individual variation in aggressiveness of response to disturbance and threats, with a similar occasional but widely reported tendencies for aggressiveness in nest defense in many other
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clutches may start to be laid as early as mid-February if food is favorable. Egg laying in mid-February is fairly typical in Italy as well. The first egg is typically laid by mid-March in Great Britain, in late March in continental Europe and early April in
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than for those that were not based on estimates, the theory as to why it lower survival is that the additional weight burden of the radio-tags themselves may have inhibited capture of food and also made juveniles more vulnerable to goshawks.
79:, wherein the owls will nest directly on the interior hole's surface. Tree hollows used may be as much as 25 m (82 ft) above the ground, but are usually within about 12 m (39 ft) of the ground. Virtually any species of
380:, especially at dawn or early in the night. Other than scalp abrasions, occular damage can be considerable when tawny owls attack humans. Perhaps the best-known victim of the tawny owl's fierce attack was the renowned bird photographer
2023:. In Annales Zoologici Fennici (pp. 227–233). Finnish Zoological Publishing Board, formed by the Finnish Academy of Sciences, Societas Scientiarum Fennica, Societas pro Fauna et Flora Fennica and Societas Biologica Fennica Vanamo.
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often regularly utilized. Female may scratch out a shallow base in soil if present and sometimes seen to reportedly tear eggs into pieces as a cushion from their broods. Other tree nest locations have included those on top of a
244:. In southern Finland, 95% of 123 nest boxes put out were occupied by tawny owls in 1970–1975, natural tree hole use decreased in same period from 48% to 3%, on top of stumps from 4% to 1% and in buildings from 15% to 1%.
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breeding attempts were recorded, a very low density to such an extent that unlike many other parts of the range that attempts to attract owls with playback were largely unsuccessful. As for breeding success near
431:, perhaps since males may be unable to continue withhold high-quality territories from competition. The 5 to 9 year old males were flexible to prey variations in ways younger males were not. In Hungary's
132:, 592 nest boxes were placed at 1.6 to 5.2 m (5.2 to 17.1 ft) high along the side of trees and 17.4% of which were used by tawnys (in latter 2 years of study up to 24.1%). In southeastern
1974:
Towards integrated population monitoring based on the fieldwork of volunteer ringers: productivity, survival and population change of Tawny Owls Strix aluco and Ural Owls Strix uralensis in Finland
59:
in 6 of 34 males, in situations where apparently a neighboring male died and was suffixed subsequently, however, one or the other nesting attempts would completely fail each time. In
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sex ratio in Great Britain or Hungary, with the ratio not changing annually unlike clutch size, brood size and reproductive success. The gender of broods were studied relatively to
256:, the mean egg laying dates were March 13th to April 3rd, with extreme dates of February 20th to April 30th, with shifts accounted for by late winter weather. In the German area of
124:, preferably those with a 15 cm × 20 cm (5.9 in × 7.9 in) entrance or larger. Of the nest boxes erected in different parts from Kielder forest and the
1805:
Overlevelse og spredning af radiomærkede unge Natugler Strix aluco i Nordsjælland. Danish with an English summary: Survival and dispersal of young tawny owls-preliminary results
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months. The species has been recorded to live to 27 years or so in captivity. If voles are scarce and weather harsh during winter, many tawny owls die by various means (
462:, anywhere from 33 to 77% of eggs produced are abandoned and may freeze, but little to no change occurs in territory occupancy. Authors inferred that the parent owls in
1339:
Parental testosterone and estradiol concentrations in the early nestling period correlate with the age-dependent breeding performance in Tawny Owls Strix aluco
1870:
Breeding performance, apparent survival, nesting location and diet in a local population of the Tawny Owl Strix aluco in Central Lithuania over the long-term
75:
sites to his mate by singing at the entrance, slipping inside and so on, with the female finally selecting one. The typical nest site of a tawny owl is a
1909:
Vegetation, precipitation and demographic response of a woodland predator: Tawny Owl Strix aluco as an indicator of soil aridity in Castelporziano forest
978:. Meyburg B.-U. & RD Chancellor (eds.). Raptor Conservation Today. World Working Group on Birds of Prey and Owls & Pica Press, London: 531, 535.
2097:
Viirulehtoja lapinpöllön pesäpaikoista ja pesimisbiotoopeista (Summary : Nest sites and nesting habitats of the Ural, Tawny and Great Grey Owls)
188:
but these are at potential risk of collapse. Occasionally, tawny owls have also been recorded nesting in abandoned burrows of larger mammals (e.g.
2053:
Distribution, numbers and breeding performance of Tawny Owls (Strix aluco) in relation to clear-cutting in a conifer forest in northern England
1587:
573:
136:, all nest boxes erected in habitat were eventually utilized by tawny owls. Many nest boxes were recorded to be used as roost sites in the
1857:
Parents raise higher proportion of high quality recruits from low fledgling production in the local population of tawny owls, Strix aluco
839:
The abundance and suitability of tree cavities and their impact on hole-nesting bird populations in beech forests of NE Iberian Peninsula
1058:
Der Einfluss der Kleinsäugerfluktuationen auf das Brüten einiger kleinsäugerfressender Vögel im südlichen Häme, Mittelfinnland 1952–1966
384:, who lost his left eye when struck by a bird he was attempting to photograph near its nest in 1937. He later called his autobiography
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it was not clear to what extent higher breeding success to attributable to hormonal levels versus experience is unclear. A testing of
332:
269:, the laying of clutch is often either delayed or does not occur at all. Due to the warmer average ambient temperatures and access to
1617:
Post-hatching testosterone concentration reflects nestling survival and pre-fledging offspring condition in the Tawny Owl Strix aluco
631:
1766:
Spatial and begging behaviours of juvenile Tawny Owls (Strix aluco) from fledging to independence under contrasting food conditions
2055:. Birds of Prey in a Changing Environment'.(Eds DBA Thompson, SM Redpath, AH Fielding, M. Marquiss and CA Galbraith.) pp, 111–129.
1245:
Recherche sur le regime alimentaire de la Chouette hulotte, Strix aluco, par la methode de a photographie sur pellicule infrarouge
1158:
Breeding of the Tawny Owl Strix aluco in Finland: responses of a southern colonist to the highly variable environment of the North
1352:
The influence of parental age and weather on testosterone concentration and offspring survival in broods of tawny owl Strix aluco
486:
1042:
Brutbiologie und den Bestand steuernde Faktoren bei Waldkauz (Strix aluco) und Waldohreule (Asio otus) in der Schwäbischen Alb
1403:
Melanin-based colour polymorphism signals aggressive personality in nest and territory defence in the tawny owl (Strix aluco)
120:. Natural holes in trees are often the most frequently used nesting site, followed closely in recent decades many artificial
273:, wintertime egg laying in human developed areas is now known to be commonplace: with records of laying in late December in
83:
tree may be used provided holes are available. These tree cavities may be of any origin, with trees that grow large such as
773:
Correlates of hoot rate and structure in male Tawny Owls Strix aluco: implications for male rivalry and female mate choice
301:. One clutch is laid per year but rarely replacement clutches have been reported if an entire clutch is lost. A record in
1883:
L'influence du regime alimentaire sur la reproduction des Chouettes hulottes, Strix aluco dans les foreˆts bourguignonnes
976:
Reproductive output of the Tawny Owl Strix aluco in relation to small mammal dynamics in intensively cultivated farmland
368:
1300:
Feeding effort of male Tawny Owls Strix aluco follows a fixed schedule: a field experiment in the early nestling period
1885:. In Juillard, M. (ed.) Rapaces nocturnes, pp. 33–6. Ed. Nos Oiseaux. Scriptura, S.A., Porrentruy (JU), Switzerland.
826:
The role of forest age, habitat quality, food resources and weather conditions for Tawny Owl Strix aluco populations
349:
1271:
Apport de proies et croissance des jeunes chez les Chouettes hulottes, Strix aluco, reproduisant dans des etables
453:
Of 562 eggs laid in Great Britain, 314 young hatched, with 44% lost before hatching and 2% lost before fledging.
21:
1844:
Effects of age composition of pairs and weather condition on the breeding performance of tawny owls, Strix aluco
1315:. In Annales Zoologici Fennici (Vol. 46, No. 4, pp. 302–311). Finnish Zoological and Botanical Publishing Board.
491:
2021:
Productivity and density of tawny owls Strix aluco in relation to the structure of a spruce forest in Britain
1401:
Da Silva, A., Van den Brink, V., Emaresi, G., Luzio, E., Bize, P., Dreiss, A. N., & Roulin, A. (2013).
760:
The effects of territorial behaviour on the stability and dispersion of tawny owl (Strix aluco) populations
2203:
2193:
675:
Dementiev, G. P., Gladkov, N. A., Ptushenko, E. S., Spangenberg, E. P., & Sudilovskaya, A. M. (1966).
397:
1922:
The breeding success of tawny owls (Strix aluco) in a Mediterranean area: a long-term study in urban Rome
1719:
Dispersal behavior and survival of juvenile Tawny owls (Strix aluco) during the low point in a vole cycle
1961:
Effects of variable feeding conditions on the Tawny Owl Strix aluco near the northern limit of its range
1779:
Parent-offspring conflict over duration of parental care and its consequences in tawny owls Strix aluco
1656:
Oxygen consumption in offspring tawny owls Strix aluco is associated with colour morph of foster mother
1443:
Fifteen years of observations on the reproductions of a forest population of a Tawny Owls (Strix aluco)
1287:
Untersuchungen uber die Futterungsaktivitat des Waldkauzes (Strix aluco L.) wahrend eiener Brutperiode
2135:
181:
989:
Ergebnisse einer mehrjährigen Studie an einer Population des Waldkauzes (Strix aluco) in West-Berlin
917:
Value of nest boxes for population studies and conservation of owls in coniferous forests in Britain
865:
Tawny owl (Strix aluco) predation in a pristine deciduous forest (Bialowieza National Park, Poland)
358:
2039:. Proceedings of the Royal Society of London. Series B: Biological Sciences, 264(1385), 1111–1116.
1630:
Das Verhalten gefangener Waldohreulen (Asio otus otus) und Waldkäuze (Strix aluco aluco) zur Beute
1232:
Le régime alimentaire d'une population forestière de Chouettes hulottes (Strix aluco) en Bourgogne
2037:
Does variation of sex ratio enhance reproductive success of offspring in tawny owls (Strix aluco)
185:
747:
Analysis of genetic parentage in the tawny owl (Strix aluco) reveals extra-pair paternity is low
699:
Fünfjährige Beobachtungen an einer Population des Waldkauzes (Strix aluco) im Berliner Grunewald
2198:
2084:
Nouvelles donnees suisses sur la longevite de la Chouette hulotte (Strix aluco) dans la nature
1583:
627:
569:
1896:
Female colour polymorphism covaries with reproductive strategies in the tawny owl Strix aluco
252:
Laying normally begins in March-early April, sometimes as early as February. Of 344 nests in
2143:
1999:
169:
141:
117:
113:
2175:
The long-term effect of fitting back-mounted radio tags to juvenile tawny owls Strix aluco
1792:
Using counts of begging young to estimate post-fledging survival in tawny owls Strix aluco
432:
340:
270:
193:
157:
1654:
Roulin, A., Bize, P., Tzaud, N., Bianchi, M., Ravussin, P. A., & Christe, P. (2005).
1169:
Piault, R., Gasparini, J., Bize, P., Paulet, M., McGraw, K. J., & Roulin, A. (2008).
2139:
2035:
Appleby, B. M., Petty, S. J., Blakey, J. K., Rainey, P., & MacDonald, D. W. (1997).
1831:
Age-dependent diet change, parental care and reproductive cost in tawny owls Strix aluco
1753:
A radio tracking study of post-fledging mortality and movements of Tawny Owls in Argyll
1073:. Communications of the Baltic Commission for the study of bird migration, 17: 123–136.
943:
Ecology of the tawny owl Strix aluco in the spruce forests of Northumberland and Argyll
930:
Occupancy rate and habitat variables influencing nest-box use by tawny owls Strix aluco
559:
463:
454:
407:
323:
290:
161:
2162:
Estimating components of variance in demographic parameters of Tawny Owls, Strix aluco
2110:
Om dodligheten under vinterhalvaret hos kattigglot (Strix a. aluco L.) i Mellansverige
1082:
Zuberogoitia, I., Martínez, J. A., Iraeta, A., Azkona, A., & Castillo, I. (2004).
721:
A population study of the Tawny Owl Strix aluco) and its main prey species in woodland
353:
of the owl's broods and most such young usually died during the early nesting period.
16:
2187:
2147:
2003:
1818:
The role of food supply in the dispersal behaviour of juvenile Tawny Owls Strix aluco
852:
Wood quality and the Tawny Owl Strix aluco in different forest types of central Italy
482:
310:
1258:
Moult in Tawny Owls Strix aluco in relation to food supply and reproductive success
1171:
Experimental support for the makeup hypothesis in nestling tawny owls (Strix aluco)
1145:
Over de opzienbarende kolonisatie van de Bosuil Strix aluco in Groningen en Drenthe
402:
381:
345:
257:
213:
177:
149:
1129:
Breeding of Tawny Owls Strix aluco in rural and urban habitats in southern Finland
27:
446:
328:
262:
125:
76:
1313:
Factors affecting reproduction in the tawny owl Strix aluco in southern Finland
220:. Also rarer still nests have been reported in the recesses of stone walls, in
891:
Wykorzystanie skrzynek lęgowych przez puszczyki Strix aluco w środkowej Polsce
477:
428:
294:
165:
39:
1907:
Fanfani, A., Manes, F., Moretti, V., Ranazzi, L., & Salvati, L. (2015).
904:
The design and use of a nestbox for Tawny Owls Strix aluco in upland forests
745:
Saladin, V., Ritschard, M., Roulin, A., Bize, P., & Richner, H. (2007).
427:
older than this the male breeding output begins to decline, possibly due to
274:
80:
48:
35:
1604:
Tawny Owls Strix aluco with reliable food supply produce male-biased broods
1816:
Coles, C. F., Petty, S. J., MacKinnon, J. L., & Thomas, C. J. (2003).
436:
415:
298:
237:
225:
133:
121:
104:
1935:
Breeding biology of the Tawny Owl Strix aluco in the forests of Burgundy
2173:
Petty, S. J., Appleby, B. M., Coles, C. F., & Julliard, R. (2004).
863:
Jedrzejewski, W., Jedrzejewska, B., Szymura, A., & Zub, K. (1996).
377:
336:
306:
302:
266:
241:
221:
217:
204:). Other nesting locations recorded for the species have included bare
189:
92:
229:
1084:
Possible first record of double brooding in the tawny owl Strix aluco
459:
411:
373:
286:
278:
253:
201:
129:
56:
52:
1988:
Predators control post-fledging mortality in tawny owls, Strix aluco
1948:
Der Waldkauz (Strix aluco) im bebauten Stadtgebiet von Berlin (West)
1735:
Overskaug, K., Bolstad, J. P., Sunde, P., & ⵁien, I. J. (1999).
176:
while the sometimes recorded as used smaller nests such as those of
2069:
Glutz von Blotzheim, U. N., Bauer, K. M., & Bezzel, E. (1980).
1894:
Roulin, A., Ducret, B., Ravussin, P. A., & Altwegg, R. (2003).
928:
Sacchi, R., Galeotti, P., Boccola, S., & Baccalini, F. (2004).
1273:. In Juillard, M (ed.) Rapaces nocturnes ,pp.299–316. Nos Oiseaux.
893:. Studia i Materiały Centrum Edukacji Przyrodniczo-Leśnej, 13(2 ).
205:
173:
137:
108:
100:
96:
88:
60:
44:
26:
15:
1509:
En nordsjaellansk Natugle-bestand (Strix aluco L.) i yngletiden.
1326:
Factors affecting timing of breeding in the Tawny Owl Strix aluco
1098:
Dambiermont, J. L., Francotte, J. P., & Collette, P. (1967).
1868:
Grašytė, G., Rumbutis, S., Dagys, M., & Treinys, R. (2016).
1615:
Sasvári, L., Nishiumi, I., Péczely, P., & Hegyi, Z. (2010).
1100:
Notes sur la nidification des Hulottes (Strix aluco) en nichoirs
441:
282:
233:
209:
145:
144:
hole. This species may too nest in nest of larger birds such as
72:
1461:
The Natural Control of a Population of Tawny Owl (Strix aluco)
84:
1365:
Beobachtungen zur Jugendentwicklung einigen Eulcn (Strigidae)
1523:
Hosking, E. J., Newberry, C. W., & Smith, S. G. (1945).
1182:
Makatsch, W. (1976). Die Eier der Vögel Europas. Leipzig, 2.
1022:
Onset of breeding in Tawny Owl Strix aluco in eastern Latvia
837:
Camprodon, J., Salvanyà, J., & Soler-Zurita, J. (2008).
828:. Polish Journal of Environmental Studies, 19(5), 1039–1043.
335:
were weighed about the condition of parents in a study from
1829:
Sasvári, L., Hegyi, Z., Csörgõ, T., & Hahn, I. (2000).
1579:
An Eye for a Bird: The Autobiography of a Bird Photographer
958:. Biology and conservation of northern forest owls, 81–86.
736:. Biology and conservation of northern forest owls, 81–86.
396:
Young begin to call in about 24 hours before they hatch.
915:
Petty, S. J., Shaw, G., & Anderson, D. I. K. (1994).
1701:
Southern, H. N., Vaughan, R., & Muir, R. C. (1954).
1405:. Behavioral Ecology and Sociobiology, 67(7), 1041–1052.
679:. Israel Program for Scientific Translations, Jerusalem.
2164:. Animal Biodiversity and Conservation, 27(1), 489–502.
1602:
Desfor, K. B., Boomsma, J. J., & Sunde, P. (2007).
824:
Wiącek, J., Polak, M., & Grzywaczewski, G. (2010).
1737:
Fledgling behavior and survival in northern tawny owls
1511:. Dansk Or- nithologisk Forenings Tidsskrift, 55: 1–5.
1354:. Behavioral Ecology and Sociobiology, 56(3), 306–313.
1193:
Hunting ranges and feeding ecology of owls in farmland
850:
Salvati, L., Manganaro, A., & Ranazzi, L. (2002).
2124:
Climate change increases the risk of malaria in birds
1920:
Ranazzi, L., Manganaro, A. & Salvati, L. (2000).
1419:
Defence as parental care in tawny owls (Strix aluco)
1206:
Prey taken by Tawny Owls during the breeding season
1020:Grandāns, G., Keišs, O., & Avotiņš, A. (2009).
815:. Birds of Western Palearctic. Update, 3(1), 43–77.
63:, 3 of 22 territories included two mature females.
1350:Sasvári, L., Péczely, P., & Hegyi, Z. (2004).
1337:Sasvári, L., Péczely, P., & Hegyi, Z. (2008).
956:Mate and nest-site fidelity in Ural and Tawny owls
734:Mate and nest-site fidelity in Ural and Tawny owls
1703:The behaviour of young Tawny Owls after fledging
1441:Delmée, E., Dachy, P., & Simon, P. (1978).
289:. They tend to lay their clutches earlier than
1094:
1092:
1036:
1034:
1032:
1030:
376:(at times knocking them out of the trees) and
1731:
1729:
1727:
945:(Doctoral dissertation, The Open University).
919:. Journal of Raptor Research, 28(3), 134–142.
906:. Quarterly Journal of Forestry, 81, 103–109.
8:
1950:. Beiträge zur Vogelkunde, 26(3/4), 157–171.
1807:. Dansk Omitologisk Tidsskrift, 93, 267–270.
1751:Petty, S. J., & Thirgood, S. J. (1989).
1697:
1695:
1693:
1113:Legselgrootte bij de Bosuil (Strix aluco L.)
1044:. Journal für Ornithologie, 119(4), 429–440.
2031:
2029:
1898:. Journal of Avian Biology, 34(4), 393–401.
1781:. Journal of Avian Biology, 39(2), 242–246.
1679:
1677:
1582:. London, Hutchinson & Co. p. 20.
1503:
1501:
1499:
1497:
1495:
1455:
1453:
1451:
1123:
1121:
1003:
1001:
999:
997:
671:
669:
667:
2160:Francis, C. M., & Saurola, P. (2004).
2051:Petty, S. J., & Thomas, C. J. (2003).
1790:Sunde, P., & Markussen, B. E. (2005).
1768:. Journal of Ornithology, 157(4), 961–970.
1669:Young Tawny Owls leaving nest at early age
1658:. Journal of Ornithology, 146(4), 390–394.
1519:
1517:
1397:
1395:
1052:
1050:
970:
968:
966:
964:
749:. Journal of Ornithology, 148(1), 113–116.
701:. Journal für Ornithologie, 104(1), 23–57.
693:
691:
689:
687:
685:
626:(2nd ed.). London: Christopher Helm.
2047:
2045:
2015:
2013:
1846:. FOLIA ZOOLOGICA-PRAHA-, 51(2), 113–120.
1764:Sunde, P., & Naundrup, P. J. (2016).
1747:
1745:
1717:Coles, C. F., & Petty, S. J. (1997).
1437:
1435:
1433:
1431:
1429:
1427:
1413:
1411:
1281:
1279:
1247:. In: Rapaces nocturnes. Ed. Nos oiseaux.
1056:Linkola, P., & Myllymäki, A. (1969).
31:The young leave the nest before fledging.
2065:
2063:
2061:
1959:Solonen, T., & Karhunen, J. (2002).
1755:. Ringing & Migration, 10(2), 75–82.
1713:
1711:
1127:Solonen, T., & af Ursin, K. (2008).
889:Gryz, J., & Krauze-Gryz, D. (2011).
715:
713:
711:
709:
707:
615:
613:
611:
609:
607:
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554:
552:
550:
548:
546:
544:
542:
540:
538:
536:
534:
532:
530:
528:
2019:Petty, S. J. & Peace, A.J. (1989).
1972:Saurola, P., & Francis, C. (2018).
1933:Baudvin, H., & Jouaire, S. (2003).
1489:. Verlag Hoffmann & Campe. Hamburg.
1463:. The Journal of Zoology, 162: 197–285.
1389:Labitte, A (1952). Oiseaux, 22: 107–12.
1234:. Rev. Sci. Bourgogne-Nature, 4, 85–89.
1230:Baudvin, H., & Jouaire, S. (2006).
807:
805:
803:
801:
723:. D. Phil Thesis, University of Oxford.
620:König, Claus; Weick, Friedhelm (2008).
603:
601:
599:
597:
595:
593:
591:
589:
587:
585:
526:
524:
522:
520:
518:
516:
514:
512:
510:
508:
504:
1685:Beobachtungen an einem Waldkauzpärchen
1576:Hosking, Eric; Lane, Frank W. (1972).
1139:
1137:
1069:Strazds, M. & Strazds, A. (1985).
799:
797:
795:
793:
791:
789:
787:
785:
783:
781:
775:. Journal of Avian Biology, 29, 25–32.
653:
651:
649:
647:
645:
643:
71:The male advertises several potential
1872:. Acta Ornithologica, 51(2), 163–175.
1855:Sasvári, L., & Hegyi, Z. (2010).
1842:Sasvari, L., & Hegyi, Z. (2002).
1302:. Acta ornithologica, 45(2), 181–188.
1298:Sasvári, L., & Hegyi, Z. (2010).
1260:. Raptor Conservation Today, 521–530.
1173:. Behavioral Ecology, 19(4), 703–709.
974:Plesnik, J., & Dusik, M. (1994).
867:. Journal of animal ecology, 105–120.
568:. London, Collins. pp. 209–219.
7:
2095:Lahti, E. & Mikkola, H. (1974).
1911:. Rendiconti Lincei, 26(3), 391–397.
1833:. Acta Oecologica, 21(4–5), 267–275.
1195:. Ph.D. thesis, Aberdeen University.
1024:. LATVIJAS UNIVERSITĀTES RAKSTI, 81.
562:; Cameron, Ad (illustrator) (1988).
2177:. Wildlife biology, 10(1), 161–170.
1071:Birds wintering in the town of Riga
841:. Acta Ornithologica, 43(1), 17–31.
1859:. Folia Zoologica, 59(3), 206–215.
762:. Journal of Zoology, 1(1), 21–48.
212:of heavy tree trunks, on the bare
14:
1538:An unusually aggressive Tawny Owl
1378:Tawny Owl nesting in factory wall
1221:. London Bird Reports, 29: 56–72.
677:Birds of the Soviet Union, vol. 1
2148:10.1111/j.1365-2486.2010.02346.x
2071:Handbuch der vögel mitteleuropas
2004:10.1111/j.0030-1299.2005.14069.x
1986:Sunde, Peter (September 2005). "
1976:. Bird Study, 65(sup1), S63-S76.
1963:. Ornis Fennica, 79(3), 121–131.
1219:The food of Tawny Owls in London
932:. AVOCETTA-PARMA-, 28(1), 25–30.
2122:GaramszegI, László Z. (2011). "
1924:. J Raptor Res, 34(4), 322–326.
1421:. Behaviour, 102(3–4), 213–230.
1160:. Ornis Fennica, 82(3), 97–106.
954:Saurola>Saurola, P. (1987).
565:Owls of the Northern Hemisphere
471:Longevity and natural mortality
1739:. The Condor, 101(1), 169–174.
1645:. Ed. Elsevier Sequoïa, Paris.
1367:. Z. Tierpsychol. 28: 494–504.
1289:. Beitr. Vogelkd, 18, 156–161.
1147:. Drentse vogels, 5(1), 43–47.
1060:. Ornis Fennica, 46(2), 45–78.
661:. Running Press, Philadelphia.
1:
1794:. Bird Study, 52(3), 343–345.
1553:. British Birds, 28: 130–132.
1540:. British Birds, 58: 343–344.
1476:. British Birds, 59: 108–109.
1131:. Bird Study, 55(2), 216–221.
1705:. Bird Study, 1(3), 101–110.
1328:. Open Ornithol J, 6, 40–51.
2112:. Var Fagelv., 17: 273–280.
2086:. Nos Oiseaux, 42: 121–123.
1619:. Ornis Fennica, 87(1), 26.
854:. Ornis Svecica, 12, 47–51.
2220:
1937:. Vogelwelt, 124, 289–294.
1564:Tawny Owl attacking Marten
1445:. Gerfaut, 68(4), 590–650.
1086:. Ardeola, 51(2), 437–439.
350:Danube-Ipoly National Park
1380:. British Birds, 39: 155.
758:Hirons, G. J. M. (1985).
265:. In very snowy years in
22:Museum Wiesbaden, Germany
1820:. Ibis, 145(2), E59-E68.
1671:. British Birds, 38: 80.
1643:La hulotte et son régime
1363:Scherzinger, W. (1971).
1208:. Ibis, 111(3), 293–299.
1204:Southern, H. N. (1969).
1040:Rockenbauch, D. (1978).
348:in owl offspring within
2099:. Savon luonto 6: 1–10.
1606:. Ibis, 149(1), 98–105.
1459:Southern, H.N. (1970).
1269:van Veen, J.C. (1990).
719:Hirons, G.J.R. (1976).
433:Pilis Biosphere Reserve
116:and on top of the tree
2082:Jeanmonod, J. (1993).
1551:An attacking Tawny Owl
1485:Steinbach, G. (1980).
1341:. Orn Fenn, 85, 46–54.
297:and much earlier than
200:) as well as those of
32:
24:
2128:Global Change Biology
1946:Wendland, V. (1980).
1683:Stülcken, K. (1961).
1667:Weller, L.G. (1944).
1549:Cadman, W.A. (1934).
1474:Aggressive Tawny Owls
1256:Petty, S. J. (1994).
1011:. T. & AD Poyser.
991:. Orn. Min. 24: 3, 7.
987:Wille, H. G. (1972).
941:Petty, S. J. (1992).
902:Petty, S. J. (1987).
813:Strix aluco Tawny Owl
811:Galeotti, P. (2001).
771:Galeotti, P. (1998).
697:Wendland, V. (1963).
398:Asynchronous hatching
182:Eurasian sparrowhawks
30:
19:
1881:Baudvin, H. (1990).
1562:Szomjas, L. (1955).
1536:Boswall, J. (1965).
1507:Andersen T. (1961).
1376:Cassidy, J. (1946).
1324:Solonen, T. (2013).
1311:Solonen, T. (2009).
1191:Hardy, A.R. (1977).
1156:Solonen, T. (2005).
1115:. Limosa, 42: 79–81.
1007:Mikkola, H. (1983).
732:Saurola, P. (1987).
392:Development of young
281:and late January in
2140:2011GCBio..17.1751G
2108:Edberg, R. (1958).
1641:Guerin, G. (1932).
1417:Wallin, K. (1987).
1285:Ritter, F. (1972).
1243:de Boe, J. (1990).
1111:Smeenk, C. (1969).
359:distraction display
346:testosterone levels
277:, early January in
186:common wood pigeons
2073:. Aula, Wiesbaden.
1803:Sunde, P. (1999).
1777:Sunde, P. (2008).
1687:. Falke, 8, 39–45.
1632:. Behaviour, 1–95.
1628:Räber, H. (1949).
1566:. Aquila, 59: 450.
1525:Birds of the Night
1487:Die Welt der Eulen
1472:Dobbs, A. (1966).
1217:Beven, G. (1965).
318:Parental behaviour
126:Glenbranter forest
33:
25:
1589:978-0-09-104460-2
1102:. Aves, 4, 31–47.
876:Mebs, T. (1980).
659:Owls of the world
657:Hume, R. (1991).
623:Owls of the World
575:978-0-00-219493-8
386:An Eye for a Bird
333:Instrinic factors
271:pestilent rodents
170:northern goshawks
55:were reported at
2211:
2178:
2171:
2165:
2158:
2152:
2151:
2134:(5): 1751–1759.
2119:
2113:
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2100:
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2008:
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1189:
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1174:
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1148:
1143:Bos, J. (1992).
1141:
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724:
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695:
680:
673:
662:
655:
638:
637:
617:
580:
579:
556:
422:Breeding success
341:steroid hormones
158:Eurasian magpies
142:black woodpecker
20:Egg, Collection
2219:
2218:
2214:
2213:
2212:
2210:
2209:
2208:
2184:
2183:
2182:
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2120:
2116:
2107:
2103:
2094:
2090:
2081:
2077:
2068:
2059:
2050:
2043:
2034:
2027:
2018:
2011:
1985:
1984:
1980:
1971:
1967:
1958:
1954:
1945:
1941:
1932:
1928:
1919:
1915:
1906:
1902:
1893:
1889:
1880:
1876:
1867:
1863:
1854:
1850:
1841:
1837:
1828:
1824:
1815:
1811:
1802:
1798:
1789:
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1776:
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1763:
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1623:
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1601:
1597:
1590:
1575:
1574:
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1557:
1548:
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1522:
1515:
1506:
1493:
1484:
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1471:
1467:
1458:
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1425:
1416:
1409:
1400:
1393:
1388:
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1375:
1371:
1362:
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1336:
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1323:
1319:
1310:
1306:
1297:
1293:
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1268:
1264:
1255:
1251:
1242:
1238:
1229:
1225:
1216:
1212:
1203:
1199:
1190:
1186:
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1177:
1168:
1164:
1155:
1151:
1142:
1135:
1126:
1119:
1110:
1106:
1097:
1090:
1081:
1077:
1068:
1064:
1055:
1048:
1039:
1028:
1019:
1015:
1006:
995:
986:
982:
973:
962:
953:
949:
940:
936:
927:
923:
914:
910:
901:
897:
888:
884:
878:Eulen und Käuze
875:
871:
862:
858:
849:
845:
836:
832:
823:
819:
810:
779:
770:
766:
757:
753:
744:
740:
731:
727:
718:
705:
696:
683:
674:
665:
656:
641:
634:
619:
618:
583:
576:
560:Voous, Karel H.
558:
557:
506:
501:
473:
424:
416:Gribskov forest
394:
369:desensitization
320:
291:long-eared owls
250:
194:European badger
162:common buzzards
69:
12:
11:
5:
2217:
2215:
2207:
2206:
2201:
2196:
2186:
2185:
2180:
2179:
2166:
2153:
2114:
2101:
2088:
2075:
2057:
2041:
2025:
2009:
1998:(3): 461–472.
1978:
1965:
1952:
1939:
1926:
1913:
1900:
1887:
1874:
1861:
1848:
1835:
1822:
1809:
1796:
1783:
1770:
1757:
1741:
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1707:
1689:
1673:
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1356:
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1330:
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1291:
1275:
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1249:
1236:
1223:
1210:
1197:
1184:
1175:
1162:
1149:
1133:
1117:
1104:
1088:
1075:
1062:
1046:
1026:
1013:
1009:Owls of Europe
993:
980:
960:
947:
934:
921:
908:
895:
882:
869:
856:
843:
830:
817:
777:
764:
751:
738:
725:
703:
681:
663:
639:
632:
581:
574:
503:
502:
500:
497:
472:
469:
464:Kielder Forest
455:Cambridgeshire
423:
420:
408:Kielder Forest
393:
390:
319:
316:
249:
246:
208:, between the
68:
65:
13:
10:
9:
6:
4:
3:
2:
2216:
2205:
2204:Bird breeding
2202:
2200:
2197:
2195:
2194:Strix (genus)
2192:
2191:
2189:
2176:
2170:
2167:
2163:
2157:
2154:
2149:
2145:
2141:
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2079:
2076:
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2066:
2064:
2062:
2058:
2054:
2048:
2046:
2042:
2038:
2032:
2030:
2026:
2022:
2016:
2014:
2010:
2005:
2001:
1997:
1993:
1989:
1982:
1979:
1975:
1969:
1966:
1962:
1956:
1953:
1949:
1943:
1940:
1936:
1930:
1927:
1923:
1917:
1914:
1910:
1904:
1901:
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633:9781408108840
629:
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519:
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513:
511:
509:
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498:
496:
493:
488:
487:anthropogenic
484:
483:avian malaria
479:
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461:
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451:
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438:
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430:
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311:Great Britain
308:
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264:
259:
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247:
245:
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242:church towers
239:
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159:
155:
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150:common ravens
147:
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114:Witch's broom
110:
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78:
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66:
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62:
58:
54:
50:
46:
41:
37:
29:
23:
18:
2174:
2169:
2161:
2156:
2131:
2127:
2123:
2117:
2109:
2104:
2096:
2091:
2083:
2078:
2070:
2052:
2036:
2020:
1995:
1991:
1987:
1981:
1973:
1968:
1960:
1955:
1947:
1942:
1934:
1929:
1921:
1916:
1908:
1903:
1895:
1890:
1882:
1877:
1869:
1864:
1856:
1851:
1843:
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1830:
1825:
1817:
1812:
1804:
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1791:
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1760:
1752:
1736:
1718:
1702:
1684:
1668:
1663:
1655:
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1624:
1616:
1611:
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1598:
1580:
1577:
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1563:
1558:
1550:
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1532:
1524:
1508:
1486:
1481:
1473:
1468:
1460:
1442:
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1402:
1385:
1377:
1372:
1364:
1359:
1351:
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1325:
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1312:
1307:
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1192:
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1128:
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1107:
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1016:
1008:
988:
983:
975:
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942:
937:
929:
924:
916:
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903:
898:
890:
885:
877:
872:
864:
859:
851:
846:
838:
833:
825:
820:
812:
772:
767:
759:
754:
746:
741:
733:
728:
720:
698:
676:
658:
624:
621:
566:
563:
474:
452:
425:
410:, the young
403:testosterone
395:
385:
382:Eric Hosking
363:
355:
329:Ythan Valley
321:
258:Swabian Jura
251:
214:forest floor
206:cliff ledges
197:
172:and various
154:Corvus corax
153:
70:
45:Tegel forest
34:
880:. Stuggart.
492:radiotagged
447:west Berlin
322:The female
295:little owls
263:Scandinavia
198:Meles meles
166:black kites
160:as well as
77:tree hollow
51:. Cases of
2188:Categories
1527:. Collins.
499:References
478:starvation
429:senescence
216:and among
122:nest boxes
40:monogamous
36:Tawny owls
378:red foxes
324:incubates
299:barn owls
275:Amsterdam
238:dovecotes
226:buildings
224:of large
81:deciduous
49:cuckoldry
2199:Ethology
437:Burgundy
222:chimneys
134:Scotland
105:hornbeam
2136:Bibcode
374:martens
337:Finland
307:Bohemia
303:Bizkaia
267:Finland
218:heather
202:rabbits
190:red fox
1586:
630:
572:
460:Wytham
412:fledge
287:Latvia
279:Munich
254:Latvia
230:cabins
174:eagles
156:) and
130:Argyll
118:canopy
93:poplar
57:Wytham
53:bigamy
1992:Oikos
364:Strix
236:, in
234:sheds
228:, on
210:roots
146:crows
138:Milan
109:alder
97:maple
89:beech
67:Nests
61:Pavia
1584:ISBN
628:ISBN
570:ISBN
442:Rome
293:and
283:Riga
248:Eggs
240:and
232:and
192:and
184:and
107:and
101:lime
73:nest
38:are
2144:doi
2126:".
2000:doi
1996:110
1990:".
128:of
85:oak
2190::
2142:.
2132:17
2130:.
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2012:^
1994:.
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388:.
285:,
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2150:.
2146::
2138::
2006:.
2002::
1592:.
636:.
578:.
196:(
152:(
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