Identification of Catharus thrushes (Hermit, Swainson’s, and Gray-cheeked Thrushes, and Veery) is often very challenging, particularly if confronted with non-vocal birds during migration. Fortunately, the Hermit Thrush is relatively distinctive amongst this group of otherwise drab, skulking birds. It is most easily distinguished from all other Catharus thrushes by the rufous rump and tail that contrasts noticeably with the brownish to greyish-brown remainder of the upperparts and head. This feature is most prominent in the subspecies inhabiting the mountains of the southern interior (auduboni) as it has the palest and greyest upperparts of any of the subspecies; it is least noticeable on northern/boreal birds (faxoni), as they can often have a slight rufous tinge to the upperparts that obscures some of the contrast. Nonetheless, this feature is still moderately to strongly obvious on all birds and is not shown by any other Catharus thrush. In addition to the contrasting rump and tail, note the relatively bold, dark spotting on the breast of the Hermit Thrush; this spotting tends to be somewhat less boldly marked on other thrush species and/or the background colour of the breast is more strongly washed with buff and is not as clean and white. The presence of a relatively bold (although thin), white to buffy-white eye-ring is also a diagnostic feature that is not shown by the other thrushes. Tthe Swainson’s Thrush shows a buffy eye-ring, but this combines with the buff lores to form a ‘spectacled’ appearance that is not shown by the Hermit Thrush.
Finally, the Hermit Thrush also provides some additional behavioural clues that can help separate it from the other Catharus thrushes. It is often less skulky than the other species, and more often forages in open habitats (lawns, gardens, etc.), although it rarely strays far from at least some form of dense cover. When foraging, the Hermit Thrush characteristically cocks and flicks its tail and flicks its wings; this behaviour is shown rarely by other thrush species.
| The soft, ethereal, flute-like song begins with a single long, clear, whistled note that is followed by several higher twirling phrases that fade towards the end; successive songs often differ in pitch and overall tonal trend (rising or falling). The song of Pacific coast birds ( guttatus, nanus) is slightly higher-pitched, harsher, and more mechanical-sounding, often with a downslurred and buzzy introductory note, while the song of northern/boreal ( faxoni) and interior ( auduboni) birds is somewhat purer and more liquid-sounding. Calls include a low, soft, dry chup or chuck (slightly higher and sharper in Pacific coast and interior birds than in northern/boreal birds), and a rising, whining zweeeee. The flight call is a clear, plaintive, whistled peew. Source: Jones and Donovan (1996); Sibley (2000) | Courtship Males arrive on breeding grounds earlier than females so that territories are fully established by the time the females arrive. Courtship flights, in which the male chases the female around the territory in a rougly circular pattern, are an important component of the courtship process in this species. As the process of pair formation progresses, these flights become slower and more deliberate, with the pair often stopping occasionally and remaining motionless for several seconds before resuming the chase. Courtship chasing between the pair lasts 3-4 days, after which the male accepts the female on his territory and breeding commences.
Nest The female alone constructs the nest over a period of 7-10 following the establishment of the pair bond. The nest is a neatly constructed, compact, bulky cup of grasses, leaves, moss, twigs, strips of bark, conifer needles, plant stalks, rootlets, hair, mud, and lichens; it is lined with finer materials such as small conifer needles, fine rootlets, fine grasses, hair, moss, strips of bark, and willow catkins. The nest is 10-15 cm in diameter and 5-8 cm in depth, with the internal cup 6-7 cm wide and 3.5-5.5 cm deep. The nest is typically placed at low levels (height usually <3 m, rarely to 6 m) among conifer branches or on the ground adjacent to the bases of trees or snags, in crevices, or under fallen logs, although some are occasionally constructed in deciduous shrubs.
Eggs A clutch of (3) 4 (6) eggs is laid between late April and mid-July, with most egg-laying in the province occurring during June. The smooth, glossy, light blue to greenish-blue eggs, which are occasionally lightly flecked with brown speckles or spots, are incubated by the female for 11-13 days before hatching. Eggs occur in B.C. between late April and late July. The Hermit Thrush is an infrequent, but regular, host for nest parasitism by the Brown-headed Cowbird.
Young The young are fully altricial and downy upon hatching, with dark flesh-pink skin and patches of dark grey down on the head, wings, and lower back; the mouth is orange-yellow and the gap flanges are yellow. The nestlings are tended by both parents for (10) 12-13 (15) days before fledging and leaving the nest. After fledging, the young are tended to by the adults for an unknown period of time before dispersing and becoming fully independent. Nestlings and dependent fledglings occuir in B.C. between mid-May and late August, with most present in the province between mid-June and late July.
Source: Jones and Donovan (1996); Baicich and Harrison (1997); Campbell et al. (1997)
| The Hermit Thrush feeds primarily on invertebrates and fruits, with insects and other small invertebrates (spiders, etc.) dominating the diet during the breeding season and berries and other small fruits becoming more important during the fall and winter (where they are available). In the absence of berries and fruits in winter, this species continues to rely heavily on invertebrate prey. There are rare reports of Hermit Thrush killing and consuming small vertebrates, such as small frogs and reptiles, but this is considerably infrequent and invertebrates are by far the dominant animal prey.
Individuals often forage within dense cover, regularly occurring throughout the forest interior, although they will also venture away from cover into more open habitats for foraging, provided that dense escape cover remains nearby. Most foraging is ground-based, during which the bird moves using characteristic robin-like hops, but it will also glean food items from the lower levels (<3 m height) of brushy and forested habitat (rarely occurring into the subcanopy or even canopy). When foraging, the Hermit Thrush scans the ground or branch visually, often flicking aside vegetation to expose prey hiding underneath. It will also engage in short aerial sallies or bouts of hovering in order to pursue flying insect prey or to inspect vegetation where it is not able to secure a solid footing.
Source: Jones and Donovan (1996)
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