Strong decline in the consumption of invertebrates by Barn Owls from 1860 to 2012 in Europe

Capsule The analysis of 616 papers about the diet of the European Barn Owl Tyto alba showed that 9678 invertebrates were captured out of 3.13 million prey items (0.31%). The consumption of invertebrates strongly decreased between 1860 and 2012. This further demonstrates that the Barn Owl diet changed to a large extent during the last 150 years.     

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.     

Habitat does not influence breeding performance in a long‐term Barn Owl Tyto alba study

Capsule This study examines the relationship between habitat variables and various aspects of breeding and foraging performance for 257 Barn Owl breeding attempts involving both released and wild birds, at 86 different nest‐sites over a 14‐year period.

Aims The study aimed to: (1) provide evidence for or against the importance of foraging habitat in Barn Owl breeding performance; (2) enable identification of areas which can, and those which cannot, be expected to sustain Barn Owl populations; (3) inform the compilation of any future guidelines such that Barn Owl release schemes are more likely to succeed; and (4) allow the revision of untested concerns in terms of the likely survival or otherwise of Barn Owls in a given area.

Methods Three data sources are used to assess the proportions of various habitat types and lengths of linear features in the vicinity of each nest: (1) The Centre for Ecology and Hydrology Land Cover Map; (2) Ordnance Survey Strategi dataset; and (3) Agricultural Census data. These are linked to various aspects of breeding performance.

Results Despite the size of the dataset, the number of significant correlations between habitat type and aspects of Barn Owl breeding success was similar to that expected by chance. Sites with more unimproved grassland within 1 km of the nest did not differ from those with less, except by a significant advancement of first‐egg date.

Conclusion The paucity of significant results may be evidence that Barn Owls are in fact rather catholic and adaptable in their habitat requirements, and not as dependent upon large areas of Field Vole (or other) habitat as has often been stated.     

Tawny Owl Strix aluco as an indicator of Barn Owl Tyto alba breeding biology and the effect of winter severity on Barn Owl reproduction

In the temperate zone, food availability and winter weather place serious constraints on European Barn Owl Tyto alba populations. Using data collected over 22 years in a Swiss population, we analysed the influence of early pre‐breeding food conditions and winter severity on between‐year variations in population size and reproductive performance. To estimate pre‐breeding food conditions, we attempted a novel approach based on an index that combines Tawny Owl Strix aluco reproductive parameters and the occurrence of wood mice Apodemus sp. in their diet. Tawny Owls breed earlier in the season than Barn Owls and are strongly dependent on the abundance of wood mice for breeding. This index was strongly positively associated with the number of breeding pairs and early breeding in the Barn Owl. Winter severity, measured by snow cover and low temperatures, had a pronounced negative influence on the size of the breeding population and clutch size. Food conditions early in the breeding season and winter severity differentially affect the Barn Owl life cycle. We were able to use aspects of the ecology and demography of the Tawny Owl as an indicator of the quality of the environment for a related species of similar ecology, in this case the Barn Owl.     

Geographic and temporal variation in the consumption of bats by European Barn Owls

Capsule We report a review of the occurrence of bats in the Barn Owl diet Tyto alba in Europe. Based on 802 studies reporting 4.02 million prey items identified in pellets, 4949 were bats (0.12%). We found that bat predation decreased during the last 150 years, is more frequent on islands than mainland, and is higher in eastern than western Europe and in southern than northern Europe. Although Barn Owls usually capture bats opportunistically, they can sometimes specialize on them.     

Shrews and moles are less often captured by European Barn Owls Tyto alba nowadays than 150 years ago

Capsule: The analysis of 815 papers about the diet of the European Barn Owl Tyto alba showed that the consumption of small mammals that are insectivorous (shrews and moles) declined between 1860 and 2014. This suggests that the impoverished invertebrate communities due to global changes affected a large range of animals up to top predators.     

Prey selection in a Barn Owl Tyto alba

Capsule A breeding Barn Owl selected vole-rich habitats for hunting at both a microhabitat and landscape scale.     

Effects of the risk of competition and predation on large secondary cavity breeders

The effects of competition and risk of predation on secondary cavity breeders were examined between the 2008 and 2009 breeding seasons using an experimental design manipulating two nest entrance sizes (large entrances allowed Barn Owls (Tyto alba) to enter, while the small entrances excluded them). During the 2009 breeding season, the entrance sizes of nest boxes were exchanged, so that if during one year a nest box in a particular location had a small entrance, the second year it had a large entrance and vice versa. Barn Owls and Eurasian Kestrels (Falco tinnunculus) occupied 67.3 and 17.3%, respectively, of large entrance nest boxes. Significantly more Jackdaws (Corvus monedula), House Sparrows (Passer domesticus) and Scops Owls (Otus scops) bred in nest boxes with small than with large entrances. After nest box entrance sizes were exchanged, Barn Owls and smaller species did not breed in the same nest boxes with the new entrance size. Jackdaws probably did not breed in large entrance nest boxes due both to exploitation competition (Barn Owls and Eurasian Kestrels occupied the majority of large entrance nest boxes), and may also have avoided empty nest boxes because of the risk of interference competition; whereas smaller species may have also avoided large entrance nest boxes due to risk of predation.     

Genetic divergence analysis of the Common Barn Owl Tyto alba (Scopoli, 1769) and the Short-eared Owl Asio flammeus (Pontoppidan, 1763) from southern Chile using COI sequence

In this paper new mitochondrial COI sequences of Common Barn Owl Tyto alba (Scopoli, 1769) and Short-eared Owl Asio flammeus (Pontoppidan, 1763) from southern Chile are reported and compared with sequences from other parts of the World. The intraspecific genetic divergence (mean p-distance) was 4.6 to 5.5% for the Common Barn Owl in comparison with specimens from northern Europe and Australasia and 3.1% for the Short-eared Owl with respect to samples from north America, northern Europe and northern Asia. Phylogenetic analyses revealed three distinctive groups for the Common Barn Owl: (i) South America (Chile and Argentina) plus Central and North America, (ii) northern Europe and (iii) Australasia, and two distinctive groups for the Short-eared Owl: (i) South America (Chile and Argentina) and (ii) north America plus northern Europe and northern Asia. The level of genetic divergence observed in both species exceeds the upper limit of intraspecific comparisons reported previously for Strigiformes. Therefore, this suggests that further research is needed to assess the taxonomic status, particularly for the Chilean populations that, to date, have been identified as belonging to these species through traditional taxonomy.     

Habitat selection by a predator of rodent pests is resilient to wildfire in a vineyard agroecosystem

Conservation of uncultivated habitats can increase the potential for ecosystem services in agroecosystems, but these lands are also susceptible to wildfires in the arid western United States. In Napa Valley, California, abundant rodent pests and an interest in integrated pest management have led wine producers to use nest boxes to attract Barn Owls (Tyto furcata) to winegrape vineyards. The viability of this practice as a method to control rodent pests depends heavily on the amount of hunting effort that Barn Owls expend in vineyards, which is known to be influenced by the amount of uncultivated land cover types surrounding the nest box. Wildfires burned nearly 60,000 ha of mainly urban and uncultivated lands surrounding Napa Valley in 2017, altering Barn Owl habitats. We compared GPS tracking data from 32 Barn Owls nesting in 24 individual nest boxes before and after the fires to analyze their hunting habitat selection. Owls with burned areas available to them after the fires had home ranges that shifted toward the fires, but selection was not strongly associated with burned areas. Though there was some spatial use of burned areas, selection of land cover types was similar for birds before and after the fires and in burned and unburned areas. The strongest selection was for areas closest to the nest box, and most recorded locations were in grassland, though selection indicated that owls used land cover types in proportion to their availability. Overall, habitat selection was resilient to changes caused by wildfires. These results are important for farmers who use nest boxes as a means of rodent control, which may be affected after dramatic disturbance events, especially as wildfires increase in the western United States.     

Spatial,road geometric and biotic factors associated with Barn Owl mortality along an interstate highway

Highway programmes typically focus on reducing vehicle collisions with large mammals because of economic or safety reasons, while overlooking the millions of birds that die annually from traffic. We studied wildlife–vehicle collisions along an interstate highway in southern Idaho, USA, with among the highest reported rates of American Barn Owl Tyto furcata road mortality. Carcass data from systematic and ad hoc surveys conducted in 2004–2006 and 2013–2015 were used to explore the extent to which spatial, road geometric and biotic factors explained Barn Owl–vehicle collisions. Barn Owls outnumbered all other identified vertebrate species of roadkill and represented > 25% of individuals and 73.6% of road‐killed birds. At a 1‐km highway segment scale, the number of dead Barn Owls decreased with increasing numbers of human structures, cumulative length of secondary roads near the highway and width of the highway median. The number of dead Barn Owls increased with higher commercial average annual daily traffic (CAADT), small mammal abundance index and grass rather than shrubs in the roadside verge. The small mammal abundance index was also greater in roadsides with grass vs. mixed shrubs, suggesting that Barn Owls may be attracted to grassy portions of the highway with more abundant small mammals for hunting prey. When assessed at a 3‐km highway segment scale, the number of dead Barn Owls again increased, with higher CAADT as well as with greater numbers of dairy farms. At a 5‐km scale, the number of dead Barn Owls increased with a greater percentage of cropland near the highway. Although human conversion of the environment from natural shrub‐steppe to irrigated agriculture in this region of Idaho has probably enhanced habitat for Barns Owls, it simultaneously has increased risk for owl–vehicle collisions where an interstate highway traverses the altered landscape. We review some approaches for highway mitigation and suggest that reducing wildlife–vehicle collisions involving Barn Owls may contribute to the persistence of this species.     

Factors determining the frequency and productivity of double brooding of Barn Owls Tyto alba

Capsule: Early nesting Barn Owls Tyto alba and those that switched nest sites fledged most chicks overall because they could fit two, more productive, nesting attempts into a breeding season.

Aims: To determine the frequency and productivity of double broods in Barn Owls, and for double brooders, to determine what affects the probability of nest switching and how that affects productivity.

Methods: We monitored the first egg date of each nesting attempt, whether it was in a ‘vole year’, whether a breeding attempt was first or a second annual attempt, the number of chicks fledged from each attempt, and whether a pair switched nest sites, if breeding twice, from 602 Barn Owl breeding attempts in an area of lowland England from 1996 to 2007. General linear models were used to determine predictors of the probability that a pair had a second brood and the number of chicks fledged in each nesting attempt, and then for those owls that double brooded, which variables best predicted the probability of switching, and the number of chicks fledged from the second nest. Finally, we tested whether switching resulted in a shorter laying interval and higher annual productivity.

Results: Early nesting birds were more likely to double brood, although this was relaxed in vole years when later nesting birds also double brooded. Productivity (through increased numbers of chicks fledged or reduced chick loss) was higher the earlier a nest occurred, and there were more chicks fledged in good vole years and in second nesting attempts. Productivity, brood depletion, first clutch date and vole years did not determine whether a double brooding pair switched nesting sites. Productivity in the second nest did not change with a switch but productivity increased for early first nests and second nests with a shorter interval between the first and second nest. Switching however decreased nesting interval and nesting interval was also shorter if there were fewer fledglings from the first nest. Overall productivity was higher for pairs that switched.

Conclusions: Double brooding in Barn Owls increased seasonal productivity substantially and its occurrence depended on vole abundance or early nesting. Nest switching between broods may be a strategy for earlier laying of the second brood. Provision of alternative nest sites, close together in a Barn Owl’s home range, may allow earlier re-nesting and so increase productivity.     

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.     

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.     

Use of field margins managed under an agri-environment scheme by foraging Barn Swallows Hirundo rustica

Capsule: Barn Swallows Hirundo rustica were more likely to forage along arable field margins that were enhanced with wildflowers or legumes than control grass margins.

Aims: To determine if foraging Barn Swallows displayed preferences for specific arable field boundary habitats (grass margins versus floristically enhanced margins) that were managed as part of an agri-environment scheme. We also aim to determine how Barn Swallow food abundance related to these habitats.

Methods: Two foraging activity surveys took place on all grass and floristically enhanced margins (n?=?56) present within the 600 m foraging range of seven Barn Swallow colonies during June and July 2016. Margin habitat use was measured by recording the presence/absence of foraging individuals during surveys, the total number of individuals and by calculating an index of foraging activity. Habitat information relating to adjacent boundary type, transect crop type and neighbouring crop type were also recorded.

Results: Foraging Barn Swallows were significantly more likely to be recorded when survey transects included a floristically enhanced margin, but there was no significant impact of floristically enhanced margins on the total number of individuals recorded or on the index of foraging activity. Foraging activity was higher along grass verges and hedgerows when compared to treelines and was positively related to length weighted Diptera abundance (a measure of food biomass).

Conclusion: Our results suggest that there may be a role for floristically enhanced margins in the conservation of Barn Swallows on arable farmland. More research, however, is needed to determine whether invertebrate-rich agri-environment scheme habitats can influence colony size or improve the breeding success of this species.     

A palaeornithological assemblage from the early Pliocene of the Mediterranean island of Mallorca: Raptorial birds as bioaccumulators at Na Burguesa-1

A palaeornithological assemblage from the early Pliocene of Mallorca (Balearic Islands) is documented on 583 fossil bones from Na Burguesa-1 site. Ten different taxa have been identified: two Tytonidae, one small-sized Strigidae, one Phasianidae, one Charadriiform, and at least five Passeriformes. The specimens included in the Tytonidae correspond to a giant Barn Owl, Tyto sp. 1, with size similar to Tyto robusta, and a second Barn Owl, Tyto sp. 2, similar in size to Tyto sanctialbani. The small-sized Strigidae is attributed to Otus sp., although some of the pedal phalanges obtained are included only tentatively in this genus. The presence of these nocturnal raptorial birds combined with the prevalence of small vertebrates (mainly ranging from ca. 8 g to almost 1 kg) with practically unaltered bones suggests that this deposit was originated by the accumulation of prey remains of these owls.     

A species of Sarcocystis using owls as definitive hosts.

Sporulated oocysts found in the intestines of a Masked Owl (Tyto novaehollandiae) and a Barn Owl (T. alba) produced sarcocysts in mice. Schizonts were found in the livers of 3 mice that died at 7-8 days after dosing. Neither sarcocysts nor schizonts were found in chickens dosed with oocysts from a Masked Owl.     

Behavioural and body mass changes before egg laying in the Barn Owl: cues for clutch size determination?

To investigate laying decision and clutch size determination in indeterminate layers, we analysed in-nest activity (nest presence, and copulation, prey deliveries, and entrance frequencies) and female body mass change, as well as their relation to clutch size variation in five Barn Owl pairs (Tyto alba) nesting in eastern France. Body mass of the female and behaviour [copulation frequency, entrance frequency, and prey delivery to the nest by the male (in number and mass)] were monitored using an automated weighing system and a video camera. There was a consistent change of behaviour and foraging activity among pairs ca. 18 days before laying indicating that the females may be tied to the nest at this time. Barn Owls being indeterminate layers have their clutch size determined at the oviposition of the first egg of the clutch. Window correlation analyses between the clutch size and the female body mass gain indicate that the clutch size might be determined no later than a few days before the laying of the first egg. Our results suggest that female Barn Owls may use the pre-laying period to determine the clutch size using cues such as the male food deliveries (a proxy for male quality).     

FIRST ANNUAL REPORT ON THE RHODESIAN ORNITHOLOGICAL SOCIETY'S NEST RECORD SCHEME FOR THE YEAR ENDED 30 JUNE, 1956

MENDELSOHN, J. M. 1989. Habitat preferences, population size, food and breeding of six owl species in the Springbok Flats, South Africa. Ostrich 60:183-190.

Information on the habitat preferences, population size, food and breeding of Barn, Grass, Whitefaced, Marsh, Pearlspotted and Spotted Eagle Owls was obtained in a 6900-ha area in the Springbok Flats, South Africa. Seventy-two per cent of the area consisted of cultivated fields not usually used by owls. Hunting, roosting and nesting requirements were largely met in 1930 ha of verges, farmyards and patches of wood land ant grassland, here was an estimated total population of 303 owls in the area, giving an overall density of 22,7 ho/owl for the whole area or 6.4 ha/owl for those areas used by owls. These high densities were attributed to an abundance of Mastomys natalensis, the most important prey item for all except Pearlspotted Owls. Rates of predation on M. natalensis varied in relation to their population density, as indicated by rodent trapping results. Marsh Owls ate more insects in summer than at other times. Barn and Marsh Owls usuall laid in March-April and August-September, while other species started breeding in July-October. de timing of breeding of some owls may be related to changes in rates of recruitment of juvenile M. natalensis. Most Marsh Owl nests were placed on the southwestern sides of grass clumps or shrubs.     

The effect of elevation and habitat cover on nest box occupancy and diet composition of Boreal Owls Aegolius funereus

Capsule: Diet composition of Boreal Owls Aegolius funereus was not affected by habitat cover, but it changed along the elevational gradient.

Aims: To assess the effect of elevation and habitat cover on nest box occupancy and diet composition of a central European population of Boreal Owls.

Methods: A Boreal Owl population was studied in the ?umava Mountains, Czech Republic, at elevations from 500 to 1300?m above sea level (asl), during 1984–2005.

Results: Boreal Owls occupied more frequently nest boxes above 600?m asl, but they did not clearly prefer any elevational band. Habitat cover did not affect the number of nesting attempts. There was also no relationship between habitat cover and diet composition. However, diet composition significantly changed along the elevational gradient. In particular, the proportion of alternative prey of Boreal Owls, i.e. birds and shrews Sorex sp., rose with increasing elevation. The proportion of voles Myodes and mice Apodemus in the diet decreased with increasing elevation. Among bird prey, the proportion of finches Fringillidae positively correlated with elevation.

Conclusions: Central European Boreal Owls did not show a clear preference for any habitat cover or elevational band, but the quality of the owls’ diet significantly decreased with increasing elevation.