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Aegolius

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Aegolius
Boreal Owl
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Aves
Order: Strigiformes
Family: Strigidae
Genus: Aegolius
Kaup, 1829
Species

A. funereus
A. acadicus
A. ridgwayi
A. harrisii
†A. gradyi
†A. martae

Aegolius is a genus of small true owls. The genus name is from Latin; aegolius is a type of screech owl thought to be a bird of ill omen.[1]

Description

Aegolius owls are small, dumpy, short-tailed, and broad-winged, with large, round facial discs. The species varies from 18–27 cm in length. These owls take mainly rodents and other small mammals as their prey, but also feed on birds, bats, insects, and other invertebrates according to what is available. They are dark brown or black above, and whitish or buff below, marked with streaks or spots in the two northern forms. The head is large, with yellow eyes and a well-defined facial disc. The flight is strong, agile, and direct. They breed in tree holes, laying several eggs. They have repetitive whistling calls in the breeding season.

Distribution and sub-species

Distribution

Three of the extant species are restricted to the New World, but the boreal owl has a circumpolar range through North America, Eurasia, the Alps, and the Rockies. Essentially nocturnal woodland owls of temperate or colder climates; the two northern species breed in North America's coniferous forests, and the unspotted saw-whet owl and buff-fronted owl (Central and South America, respectively) are species of mountain, cloud, or oak forests. They are mainly resident birds, but the northern species at least sometimes move south or to lower altitudes in autumn. The movements are difficult to monitor due to the problems of detecting these nocturnal owls outside the breeding season, when they are not calling.

Sub-species

Mating system

Aegolius owls have a very diverse mating system containing multiple strategies. Although six species are within this genus, two of which are extinct, the majority of the information known about the mating system is based on research from the boreal owl (A. funereus) and the northern saw-whet owl (A. acadicus) in North America.[2] Both species have been shown to exhibit both monogamous and polygamous lifestyles with a focus on bigyny.[3] However, the Boreal owl has been show to exhibit biandry as well[4]

Mate choice

Territorial call of the boreal owl (A.funereus)

Vocalizations

Mate choice in this genus is largely related to auditory vocalizations (a form of sensory exploitation). A quiet species through most of the year, the northern saw-whet owl male produces a bell-like or “series song” advertisement call.[5][6] Generally, it can be heard early morning or on bright nights from March – May (the breeding season) to attract females.[7] The calls are believed to be relatively different between individuals, suggesting they may play a role in individual identification by the females.[8] After pairing with a mate, vocalizations are very limited and appear to be related to territory or offspring defence.[9]

In contrast, the boreal owl produces a “staccato song” starting around dusk, and ending around midnight in the late winter and early spring. The call serves to attract females and becomes increasingly persistent as time without a mate passes.[10][11] Some research suggests that unlike the Northern saw-whet owl, a variation of the mall call persists after mating throughout the reproductive cycle for defense, aggression, or to convey information about prey. This suggests that vocalization may be used in this species beyond mate attraction and possibly as a contact call.[12]

Typical boreal owl (A. funereus) nest

Nest and territory quality

Aside from vocalization, females in this genus may choose males based on nest or territory quality. For example, in boreal owls, the number and quality of nest holes or boxes defended by males is a factor in female reproductive effort.[13] The number and quality of nests appear to serve a direct benefit to females (direct benefit hypothesis), as it provides protection from predation, as well as access to food resources, as good nest quality can be indicated by access to prey (i.e. small mammals).[13] Female boreal owls’ reproductive success can decline in polyterritorial polygamous situations, as females are unable to discriminate previously paired and unpaired males (also known as the deception hypothesis). It is also important to note that increasing polygamy levels leads to decreased reproductive success in secondary females.[13] Limited research has been conducted into mate choice of the Northern saw-whet owl in relation to territory quality. Some researchers suggest they follow a similar trend to boreal owls, where the quality of nests is a direct benefit to the female and therefore a determining factor.[14] Northern saw-whet owls' nest locations appear less linked to the availability of small mammals, as they have a greater variety of prey options and tend to be more nomadic after each breeding season.[14][15]

Reversed size dimorphism

Lastly, size of males may play a role in mate choice in some species. The males in this genus provide direct benefit to females such as protection, territory, and resources. As a result, large male size (and smaller female size) would theoretically be more advantageous. However, in the boreal owl, this is not the case. Females tend to be larger and heavier than the male mates they choose, some suggesting this is the result of the starvation hypothesis (selection acts on females to increase ability to withstand long periods of time without food in polygamous lifestyles).[16] Another theory suggests that females purposely choose short-winged, light males, as they would be able to hunt at lower energetic costs and compete for territory more efficiently than larger, long-winged individuals.[16][17] This would provide the female with greater material benefits for her offspring. Reversed size dimorphism is also observed in northern saw-whet owls, but the differences are much more difficult to observe, as the species is smaller overall; the role of this in mate choice is unclear.[18]

Ural owl (Strix uralensis) a prime competitor of A.funereus

Contests

Relating to the observed size dimorphism in males, most species compete for territory in this genus, as it indirectly relates to better female mates.[16][17][13] The intraspecific competition tends to be dependent on individual flight ability, individuals that can fly more efficiently and effectively tend to get better territory.[16] However, interspecific competition also plays a role. Species in this genus are often smaller than other owls that have similar ranges; as a result, they often are outcompeted for territory by other species.[2][19] This is especially true in boreal owls, as their range overlaps with the much larger Ural (Strix uralensis) and Eurasian eagle owls (Bubo bubo). As a result, when these species are present, the boreal owl often mates with less desirable subdominant females.[19]

Northern saw-whet owl (A.acadicus) juveniles.

Parental Care

Boreal owl juveniles

Parental care in the boreal and northern saw-whet owls is quite similar; females incubate and brood eggs, while males often provide protection, and resources such as food and nesting sites.[2] This trend likely applies across the species in this genus, as some species may be conspecifics (i.e. northern saw-whet and unspotted saw-whet owls).[20]

In boreal owls, the level of investment provided by the male is directly related to the level of parental care effort in brooding by the female.[21] Increased resources (i.e. food) provided by the male during the nesting stage increases female effort in brooding of the offspring.[21] This is similar to the differential allocation hypothesis, which suggests that females increase their reproductive effort overall when offspring are the result of ideal mates. Brooding behavior is key to the success of owl fledglings, so when males provide adequate food, females provide adequate care.[22][21] Fewer or lighter individual fledglings are produced as polygamy rate increases and the amount of male effort becomes increasingly important in predicting female brooding effort.[23]

Information on parental care effort is limited on the northern saw-whet owl, and likely related to male provisioning rates, the extent, however, is unclear. Current research examines the effect of habitat loss on the male provisioning rates.[24]

References

  1. ^ Jobling, James A (2010). The Helm Dictionary of Scientific Bird Names. London: Christopher Helm. pp. 33, 166. ISBN 978-1-4081-2501-4.
  2. ^ a b c Johnsgard, P. A. (1988). North American owls: biology and natural history.
  3. ^ Marks, J. S., Doremus, J. H., & Cannings, R. J. (1989). Polygyny in the Northern Saw-whet Owl. The Auk, 106(4), 732-734.
  4. ^ Solheim, R. (1983). Bigyny and biandry in Tengmalm's Owl Aegolius funereus. Ornis Scandinavica, 51-57.
  5. ^ Simpson, M. B. (1972) The saw-whet owl population of North Carolina's southern Great Balsam Mountains. Chat 36:39-47.
  6. ^ Swengel, S. R., & Swengelº, A. B. (1981). Study of a Northern Saw-Whet Owl Population in Sauk County, Wisconsin'. METHODS, 178(1953).
  7. ^ Walker, L. W. (1974). The Book of Owls. New York: Alfred A. Knopf.
  8. ^ Otter, K. (1996). Individual Variation in the Advertising Call of Male Northern Saw-Whet Owls (Variación Individual en las Llamadas de Aegolius Acadicus). Journal of Field Ornithology, 398-405.
  9. ^ Johns, S., G. R. A. Ebel, and A. Johns. (1978). Observations on the nesting behaviour of the saw-whet owl in Alberta. Bluejay 36:36-38.
  10. ^ Bondrup-Nielsen, S. (1978). Vocalizations, nesting and habitat preferences of the boreal owl (Aegolius funereus) in North America. M.S. thesis, Univ. of Toronto.
  11. ^ Bondrup-Nielsen, S. 1984. Vocalizations of the boreal owl, Aegolius funereus richardsoni, in North America. Canadian Field-Naturalist. 98: 191-97.
  12. ^ Meehan, R H. (1980). Behavioral significance of boreal owl vocalizations during the breeding season. M.S. thesis, University of Alaska, Fairbanks.
  13. ^ a b c d Carlsson, B. G. (1991). Recruitment of mates and deceptive behavior by male Tengmalm's owls. Behavioral Ecology and Sociobiology, 28(5), 321-328.
  14. ^ a b Marks, J. S., Nightingale, A., & McCullough, J. M. (2015). On the breeding biology of Northern Saw-whet Owls (Aegolius acadicus). Journal of Raptor Research, 49(4), 486-497.
  15. ^ Marks, J. S., & Doremus, J. H. (2000). Are northern saw-whet owls nomadic?. Journal of Raptor Research, 34(4), 299-304
  16. ^ a b c d Korpimäki, E. (1986). Reversed size dimorphism in birds of prey, especially in Tengmalm's Owl Aegolius funereus: a test of the" starvation hypothesis". Ornis Scandinavica, 326-332.
  17. ^ a b Hakkarainen, H., & Korpimäki, E. (1991). Reversed sexual size dimorphism in Tengmalm's Owl: Is small male size adaptive?. Oikos, 337-346.
  18. ^ Earhart, C. M., & Johnson, N. K. (1970). Size dimorphism and food habits of North American owls. The Condor, 72(3), 251-264.
  19. ^ a b Hakkarainen, H., & Korpimaki, E. (1996). Competitive and predatory interactions among raptors: an observational and experimental study. Ecology, 77(4), 1134-1142.
  20. ^ "Aegolius ridgwayi". Integrated Taxonomic Information System. Retrieved 15 April 2018
  21. ^ a b c Zárybnická, M., & Vojar, J. (2013). Effect of male provisioning on the parental behavior of female Boreal Owls Aegolius funereus. Zoological Studies, 52(1), 36.
  22. ^ Sheldon, B. C. (2000). Differential allocation: tests, mechanisms and implications. Trends in Ecology & Evolution, 15(10), 397-402.
  23. ^ Korpimäki, E. (1991). Poor reproductive success of polygynously mated female Tengmalm's owls: are better options available?. Animal Behaviour, 41(1), 37-47.
  24. ^ Hinam, H. L., & Clair, C. C. S. (2008). High levels of habitat loss and fragmentation limit reproductive success by reducing home range size and provisioning rates of Northern saw-whet owls. Biological Conservation, 141(2), 524-535.
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