Oenanthe oenanthe is a widespread summer visitor to most of Europe, which accounts for less than half of its global breeding range. Its European breeding population is very large (>4,600,000 pairs), and was stable between 1970-1990. Although it remained stable in various countries-particularly in eastern Europe-during 1990- 2000, the species suffered widespread declines, including in the key Turkish population, and underwent a moderate decline (>10%) overall. Consequently, this previously Secure species is now provisionally evaluated as Declining.

Breeds from high and low Arctic through boreal and temperate zones to steppe, Mediterranean, and subtropical arid zones, and from extreme continental to extreme oceanic climates, reaching Nearctic tundra from both European and Asian distribution areas. Much of this expansion must have occurred since the last glaciation and far surpasses that of other Oenanthe with which however it shares constraints of requiring ready-made rock or burrow nest-site immediately neighbouring seasonally insect-rich bare patches or short swards for easy foraging. Has exploited stony and shrub tundra, rocky slopes, scree, and alpine meadows above treeline in mountains.

In Britain and north-west Europe egg-laying starts from mid-April to June. In South and central Europe from early May to June. In Iceland from late May to late June and in Scandinavia from early to mid-May to early July. 1-2 broods. Nest is a hole in wall, among stones or rocks, in burrow, or in ruined building, will also use nest-box or holes in wide variety of man-made objects. Nest is a foundation (absent in nests in rock crevices) comprises large, untidy mass (up to 25 cm across) of dried stems of bracken, heather, and other plants, plus grass and occasional large feathers; cup more tightly woven of finer grass stems and leaves, with some moss and lichen. Clutch: 4-7 (2-9) incubated in c. 13 days (10-16) by female only, though male occasionally helps. Young fledge on average after 15 days (10-21), though most young already leave actual nest in burrow and move around in it at about 10 days.

Diet based chiefly on insects, also spiders, molluscs, and other small invertebrates, supplemented by berries. Normally locates prey visually, chiefly on ground or in low vegetation. Two main foraging techniques, which may be used in same area. 1) Running, in flat areas of short turf, runs short distance, stops to pick up item or to scan ground ahead, and then runs on. 2) Perching, in areas of scattered perches, uses these to scan ground nearby, drops down for item, and then returns to perch or moves to new one.

This species has a large global range; the total size has not yet been quantified, but the Extent of Occurrence in Africa and the Americas combined is estimated to be 2,302,600 km². It has a large global population estimated to be 2,900,000 individuals (Rich et al. 2003). Global population trends have not been quantified, but the species is not believed to approach the thresholds for the population decline criterion of the IUCN Red List (i.e. declining more than 30% in ten years or three generations). For these reasons, the species is evaluated as Least Concern.

Migratory, though North African race seebohmi probably only partially so. Winter quarters of entire world population, including birds breeding in Nearctic, in tropical Africa¾in broad belt south of Sahara from West African coast to Indian Ocean, and south in eastern Africa to northern Zambia; records of wintering elsewhere few and probably exceptional. Passage occurs on broad front across southern Europe, Mediterranean, and full length of North African coast; recorded in about equal abundance in both seasons, in contrast to many passerines. Migration seasons notably protracted. Birds leave breeding grounds chiefly from August; some movement southward noted from mid-July, with passage continuing until c. 3rd week of October, and stragglers into November. Departure from winter quarters protracted, probably especially in west, with passage noted from late January in southern Morocco, and records from mid-February to May in Algeria. Passage across North African coast and Mediterranean chiefly March-April, tailing off to mid-May. In north-west Europe, a notably early spring migrant. Thus, often the first passerine to reach Britain, where sometimes recorded early March (exceptionally late February), but more usually from mid-March with peak in early April. First arrivals in Netherlands mid-March. In Norway, arrives in south from mid-March but not present in arctic regions until mid-May. Iceland, Greenland, and east Canadian population winters from Sénégal and Sierra Leone east to Mali. Autumn migration involves south-east crossing of North Atlantic, and frequency of records from ships south-east of Greenland is clear evidence that large numbers fly non-stop from Greenland to western Europe

article number 1 Title
Stopover behaviour and departure decision of northern wheatears, Oenanthe oenanthe, facing different onward non-stop flight distances
Author(s): Volker Dierschke ,and Julia Delingat
Abstract: On the small North Sea island Helgoland (54°11??N, 07°55??E) we studied the stopover ecology of two subspecies of northern wheatear, Oenanthe oenanthe, during spring migration. Birds heading for Scand..[more]..
Source: Behav Ecol Sociobiol (2001) 50:535-545
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article number 2 Title
Differential timing of spring migration in northern wheatears Oenanthe oenanthe: hurried males or weak females?
Author(s): Volker Dierschke, Bettina Mendel
Abstract: In a field experiment on the island of Helgoland (southeast North Sea), we investigated whether migration strategy or competition between the sexes cause the differential timing of spring migration of..[more]..
Source: Behav Ecol Sociobiol (2005) 57:470-480
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article number 3 Title
Daily stopovers as optimal migration strategy in a long-distance migrating passerine: the Northern Wheatear Oenanthe oenanthe.
Author(s): Delingat J., Dierschke V., Schmaljohann H., Mendel B. & Bairlein F.
Abstract: Selection for early arrival is expected to shape optimal stopover decisions in migrating birds to minimise time spent on migration. Optimality models predict that fuel loads at departure from stopover..[more]..
Source: ARDEA 94 (3): 593-605.
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article number 4 Title
Optimal bird migration and predation risk: a field experiment with northern wheatears Oenanthe oenanthe
Author(s): HEIKO SCHMALJOHANN and VOLKER DIERSCHKE
Abstract: Experiments testing predictions of optimal migration theory so far have concentrated on time and energy as the expenses that birds strive to minimize during migration. Taking advantage of the high var..[more]..
Source: Journal of Animal Ecology 74 (1), 131-138
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article number 5 Title
MAGNETIC ORIENTATION OF MIGRATORY WHEATEARS (OENANTHE OENANTHE) IN SWEDEN AND GREENLAND
Author(s): ROLAND SANDBERG ET AL
Abstract: Orientation experiments were performed with wheatears (Oenanthe oenanthe) subjected to artificially manipulated magnetic fields, in Sweden and Western Greenland, during the autumn migration period. Th..[more]..
Source: J. exp. Biol. 155, 51-64 (1991)
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