Multiple Paternity in Polyandrous Barn Owls (Tyto alba)

In polyandrous species females produce successive clutches with several males. Female barn owls (Tyto alba) often desert their offspring and mate to produce a 2^nd annual brood with a second male. We tested whether copulating during chick rearing at the 1^st annual brood increases the male''s likelihood to obtain paternity at the 2^nd annual breeding attempt of his female mate in case she deserts their brood to produce a second brood with a different male. Using molecular paternity analyses we found that 2 out of 26 (8%) second annual broods of deserting females contained in total 6 extra-pair young out of 15 nestlings. These young were all sired by the male with whom the female had produced the 1^st annual brood. In contrast, none of the 49 1^st annual breeding attempts (219 offspring) and of the 20 2^nd annual breeding attempts (93 offspring) of non-deserting females contained extra-pair young. We suggest that female desertion can select male counter-strategies to increase paternity and hence individual fitness. Alternatively, females may copulate with the 1^st male to derive genetic benefits, since he is usually of higher quality than the 2^nd male which is commonly a yearling individual.     

The importance of micro-habitat in the breeding of Barn Owls Tyto alba

Capsule?Habitat parameters associated with 706 Barn Owl (Tyto alba) nesting boxes in Israel were analysed. Pairs bred in 259 of the boxes. The intensity of agricultural practices at nestbox sites were shown to have only a weak effect on aspects of Barn Owl breeding in this region.     

The feeding and breeding ecology of Barn Owls Tyto alba in Peninsular Malaysia

Barn Owls have only recently colonized Peninsular Malaysia, nesting in the roof spaces of houses in oil palm estates and feeding on the rats which inhabit these plantations. Pellet analysis showed that the prey spectrum was confined almost entirely to three species of the genus Rattus which are the major pests of oil palm. There was no annual variation in diet. Breeding showed a broad seasonality but occurred in all months of the year. Mean clutch and brood sizes of 6.6 and 4.6 respectively were recorded, most pairs producing two broods a year although on two occasions three were raised. Overall hatching success was 69.0% with first clutches more successful (79.9%) than second (57.3%). First broods fledged 86.1% and second broods 69.1% of young fledged. Comparison of growth rates of different sized broods suggested that there is a physiological maximum at which all broods proceed irrespective of brood size. The behaviour al changes needed in hunting techniques when colonizing dense plantations rather than the more usual open habitat of Barn Owls is discussed. The breeding strategy seems to be one of producing large clutches and broods, and frequent breeding attempts in a habitat with a high potential carrying capacity.     

Changes in the food of British Barn Owls (Tyto alba) between 1974 and 1997

Comparison of the results of a 1993–97 Barn Owl Tyto alba pellet survey with those of a similar survey from 1956–74 showed that Barn Owl diet had changed significantly. The primary differences were a widespread decrease in the percentage of Common Shrew Sorex araneus, combined with an increase in Pygmy Shrew Sorex minutus. The percentage of Wood and Yellow‐necked mice Apodemus sylvaticus and A. flavicollis and Bank Vole Clethrionomys glareolus in the diet also increased. Changes in Barn Owl diet since 1974 were independent of land‐class group, but were dependent upon region. This was due primarily to a large increase in the percentage of Apodemus spp. in Eastern England. Whilst the percentage of Pygmy Shrew in Barn Owl diet showed significant regional variation, there was no significant variation between land‐class groups. The diversity of Barn Owl diet increased between 1974 and 1997, although it was still lower in 1997 than earlier in the century. This increase was dependent upon region, but independent of land‐class group. The combined results of both surveys showed significant interland‐class group variation in dietary diversity. Changes in diet are discussed in relation to the intensification of agriculture and other changes in land management since the 1970s. The effects on Barn Owls of these changes in prey abundance are discussed, particularly in relation to the decline in Barn Owl numbers during the twentieth century.     

A preliminary assessment of the relationship between trophic variability in southern African Barn Owls Tyto alba and climate

Avery, D.M. 1999. A preliminary assessment of the relationship between trophic variability in southern African Barn Owls Tyto alba and climate. Ostrich 70 (3&4): 179–186.

The proximate purpose of the study was to investigate the possibility that micromammalian remains from archaeological sites could provide quantified data concerning past climates. Proportions of micromammalian taxa represented in Barn Owl pellets recovered from 111 roost sites in Africa south of 22°S were analysed with climate variables to determine whether there was any relationship between the two. Preliminary results indicate that some taxa, notably the gerbils Gerbillinae and Gerbillurus and mice Mastomys, will be capable of providing such data. It is clear, however, that careful attention must be paid to the compilation of the database and the nature of the evidence being employed. The disturbed nature of much vegetation in the region must be taken into consideration but it is probable that the effects of disturbance can be characterised and therefore discounted.     

Direction of movements in Hungarian Barn Owls (Tyto alba): gene flow and barriers

Abstract. An analysis of dispersal directions of the barn owl showed that all individuals immigrating to Hungary came from W‐NW‐N. It was shown that immigrating owls breed in Hungary. There is no prevailing direction in emigration from Hungary. The time of fledging does not influence the direction of movement and there is no difference between sexes concerning dispersal direction. The percentages of emigrating owls is greater than that of immigrating ones. These percentages did not differ in relation to most of the analysed countries (Germany, Italy, Switzerland, Poland and countries of the former Yugoslavia and Czechoslovakia) but it differed in relation to Austria. The degree and direction of introgression into and from the transition zone and the recent distribution of the phenotypes are discussed based on the comparative analysis of published European data. These suggest that the subspecies Tyto alba alba and Tyto alba guttata disappear by introgression, to form a phenotypically very variable species.     

Wing and tail myology of Tyto furcata (Aves,Tytonidae)

Barn Owls (Tytonidae) are nocturnal raptors with the largest geographical distribution among Strigiformes. Several osteological, morphometrical, and biomechanical studies of this species were performed by previous authors. Nevertheless, the myology of forelimb and tail of the Barn Owls is virtually unknown. This study is the first detailed myological study performed on the wing and tail of the American Barn Owl (Tyto furcata). A total of 11 specimens were dissected and their morphology and muscle masses were described. Although T. furcata has the wing and tail myological pattern present in other species of Strigiformes, some peculiarities were observed including a difference in the attachment of m. pectoralis propatagialis due to the lack of the os prominence, and the presence of an osseous arch in the radius that seems to widen the anchorage area of the mm. pronator profundus, extensor longus alulae, and extensor longus digiti majoris. Furthermore, the m. biceps brachii has an unusual extra belly that flexes the forearm. The interosseous muscles have a small size and lacks ossified tendons. This feature may be indicative of a lower specialization in the elevation and flexion of the digiti majoris. Forelimb and tail muscle mass account for 10.66 and 0.24% of the total body mass, respectively. Forelimb muscle mass value is similar to the nocturnal (Strigiformes) and diurnal (Falconidae and Accipitridae) raptors, while the tail value is lower than in the diurnal raptors (Falconidae and Accipitridae). The myological differences with other birds of prey are here interpreted in association with their “parachuting” hunting style. This work complements our knowledge of the axial musculature of the American Barn owls, and provides important information for future studies related to functional morphology and ecomorphology.     

The prey of the Barn owl (Tyto alba alba) in East Norfolk

Some 5000 Barn owl pellets, collected from sites in East Norfolk during the past decade, have been examined. The most important prey species, by weight, were the Field vole (Microtus agrestis) 52%, the Brown rat (Rattus norvegicus) 17%, and the Common shrew (Sorex araneus) 12%. The prey varies over different habitats; Wood mice (Apodemus sylvaticus) and Bank vole (Clethrionomys glareolus) forming a higher proportion in localities with hedges, scrub and woodland than in open grasslands. These results are comparable with those of other recent work. However, when compared with studies conducted over 30 years ago, it would appear that the Field vole now constitutes a higher proportion, and the Brown rat a lower proportion, of the prey taken.     

Seasonal pattern in age, sex and body condition of Barn Owls Tyto alba killed on motorways

The Barn Owl Tyto alba was the most common owl killed on motorways in northeastern France. The possible causes of this mortality and the age, sex and body condition of the road-killed birds in 1991–1994 have been investigated. The number of birds killed on roads was highest in the period from early autumn to late winter, i.e. during the non-breeding period, and showed a pattern similar to that of the temporal difference between sunset, which varies with day length, and peak of traffic, the occurrence of which is constant throughout the year. An autumnal mortality peak, concomitant with the post-fledging dispersal, was mainly of immature birds, especially females. A second mortality peak in late winter was composed mainly of mature birds, with an equal proportion of males and females. From autumn to winter, there was no significant change in body mass in the different age and sex categories of birds killed on roads, except for mature males which had a significantly lower body mass in winter. From early autumn to late winter, the mean body mass of immature owls killed on motorways did not differ significantly from that of captive immatures fed ad libitum. This suggests that the immature birds were in good body condition. In contrast, the body mass of road-killed mature females was significantly lower than that of captive mature females over the same time periods. In mature males in late winter, a drop in body mass in both road-killed and captive birds suggests an endogenous seasonal phenomenon. Except for mature females, Barn Owls killed on roads in 1991–1994 were in good body condition. This does not support the idea that only birds in poor body condition were killed. We conclude that the mortality of Barn Owls on motorways in autumn and winter was probably related to the concomitance between the peak of traffic and the onset of hunting activity and the large number and dispersal of immature individuals during the same period.     

Isolation and characterization of major histocompatibility complex (MHC) class II B genes in the Barn owl (Aves: Tyto alba)

We isolated major histocompatibility complex class II B (MHCIIB) genes in the Barn owl (Tyto alba). A PCR-based approach combined with primer walking on genomic and complementary DNA as well as Southern blot analyses revealed the presence of two MHCIIB genes, both being expressed in spleen, liver, and blood. Characteristic structural features of MHCIIB genes as well as their expression and high non-synonymous substitution rates in the region involved in antigen binding suggest that both genes are functional. MHC organization in the Barn owl is simple compared to passerine species that show multiple duplications, and resembles the minimal essential MHC of chicken.     

Covariation between plumage colour polymorphism and diet in the Barn Owl Tyto alba

Several hypotheses might explain the evolution and maintenance of colour morphs within animal populations. The 'alternative foraging strategy' hypothesis states that alternative colour morphs exploit different ecological niches. This hypothesis predicts that morphs differ in diet, either because foraging success on alternative prey species is morph-dependent or because differently coloured individuals exploit alternative habitats. I examined this prediction in the Barn Owl Tyto alba , a bird that varies in plumage coloration continuously from dark reddish-brown to white. On the European continent, Owls are light-coloured (subspecies T. a. alba ) in the south and reddish-brown ( T. a. guttata ) in the north; in central Europe the two subspecies interbreed, generating many colour variants. If plumage coloration indicates alternative foraging strategies, in sympatry dark- and light-coloured owls should consume prey species that are typical of the diets of T. a. guttata and T. a. alba in allopatry, respectively. In line with this prediction, both in allopatry and in sympatry in Switzerland T. a. guttata fed primarily upon Common Voles Microtus arvalis and T. a. alba upon Wood Mice Apodemus spp. Statistical analyses suggest that morph-dependent diet did not arise from a non-random habitat distribution of owls with respect to plumage coloration. This suggests that foraging success upon alternative prey is morph-dependent.     

Communal Roosting of Wintering Red Kites Milvus milvus (Aves,Accipitridae): Social Feeding Strategies for the Exploitation of Food Resources

Social feeding strategies of wintering red kites are analyzed in relation to age, food, roost-sites and differences from kite residents. Whereas young and adult wintering kites gathered at roost sites almost daily, adult residents did not, and immature residents only occasionally. Kites using roost sites feed more often on prey prelocated by others, while lone roosters also forage and discover food alone. After finding food, kites tend to shift to a new roost site and foraging area. Two details of the ‘information centre’ hypothesis are confirmed in our study: carcasses are unpredictably found patches, divisible between several individuals. But carcasses disappeared fast in the study area, and no increase with time in the number of birds consuming a carcass was observed, so that information transmission was unconfirmed. When kites leave the roost in groups no leader is detectable. It seems that other types of social foraging are operating, and the model best matching our results is network foraging.     

Corticosterone Promotes Scramble Competition Over Sibling Negotiation in Barn Owl Nestlings (Tyto alba)

In species with parental care, siblings compete for access to food resources. Typically, they vocally signal their level of need to each other and to parents, and jostle for the position in the nest where parents deliver food. Although food shortage and social interactions are stressful, little is known about the effect of stress on the way siblings resolve the conflict over how food is shared among them. Because glucocorticoid hormones mediate physiological and behavioral responses to stressors, we tested whether corticosterone, the main glucocorticoid in birds, modulates physical and vocal signaling used by barn owl siblings (Tyto alba) to compete for food. Although corticosterone-implanted (cort-) nestlings and placebo-nestlings were similarly successful to monopolize food, they employed different behavioral strategies. Compared to placebo-nestlings, cort-individuals reduced the rate of vocally communicating with their siblings (but not with their parents) but were positioned closer to the nest-box entrance where parents predictably deliver food. Therefore, corticosterone induced nestlings to increase their effort in physical competition for the best nest position at the expense of investment in sib?Csib communication without modifying vocal begging signals directed to parents. This suggests that in the barn owl stress alters nestlings?? behavior and corticosterone could mediate the trade-off between scramble competition and vocal sib?Csib communication. We conclude that stressful environments may prevent the evolution of sib?Csib communication as a way to resolve family conflicts peacefully.