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Long-legged buzzard

The long-legged buzzard ( rufinus) is a medium-sized in the family , notable for its robust build, long legs adapted for terrestrial hunting, and highly variable that includes light, , and dark morphs, often with prominent dark carpal patches on the undersides of the wings. Adults typically measure 50–66 cm in length, with a of 115–160 cm and weights ranging from 0.6–1.8 kg, making it one of the larger species in the genus . This inhabits open, arid landscapes such as steppes, semi-deserts, and desert edges, avoiding dense forests, and can occur from sea level up to 3,500 m in elevation. Native to a broad range across southeastern Europe, the , , and , the long-legged buzzard breeds from the and eastward to northwestern China and northern , with some populations also in the and . It is partially migratory, with northern breeding populations wintering in , the , and southern Asia, while southern races remain more sedentary. The species prefers hunting from elevated perches like rocks, posts, or trees in dry grasslands, meadows, and croplands, where it scans for prey over vast open areas. Its diet consists primarily of small mammals, including rodents like gerbils, voles, ground squirrels, and rats, as well as lagomorphs such as hares and rabbits, supplemented by birds, reptiles (snakes and ), amphibians, , and occasionally carrion or prey disturbed by grass fires and vehicles. occurs from March to June in most regions, with pairs building large stick nests on cliffs, crags, trees, shrubs, or even abandoned buildings; clutches of 2–4 white eggs, blotched with reddish-brown, are incubated for about 28 days, and young after roughly 45 days. Two are recognized: the nominate B. r. rufinus (widespread in ) and B. r. cirtensis (darker-plumaged, in and Arabia). Although populations have declined locally in and Arabia due to habitat loss and persecution, the global estimate of 100,000–499,999 mature individuals remains stable overall, leading to its classification as Least Concern on the . Conservation efforts, including research by organizations like The Peregrine Fund, focus on monitoring and mitigating threats in key breeding areas.

Taxonomy and systematics

Etymology and classification

The binomial name Buteo rufinus combines the name , derived from the Latin term for the , with the specific epithet rufinus, a form of rufus meaning "" in Latin, referring to the bird's characteristic tones. The long-legged buzzard is placed within the family , the hawks, eagles, and allies, and the , which encompasses various buzzards and hawks worldwide. It exhibits morphological similarities to the (Buteo lagopus), including body proportions and flight style, though the two occupy distinct biogeographic realms. First recognized as a distinct species by German naturalist Philipp Jakob Cretzschmar in 1829, B. rufinus has undergone taxonomic scrutiny, with early classifications emphasizing its separation from other Eurasian buzzards based on morphology. Phylogenetic analyses using mitochondrial and nuclear DNA confirm its position in a monophyletic Buteo clade, showing minimal genetic divergence from congeners like B. buteo, indicative of Pleistocene-era radiation driven by climatic shifts and .

Subspecies

The Long-legged buzzard ( rufinus) is currently recognized as comprising two main subspecies, distinguished primarily by morphological differences and geographic ranges. The nominate subspecies, B. r. rufinus, inhabits southeastern , , and , extending eastward through the Transcaucasia, , , and to northwestern China, and southward to northern Pakistan and northwestern (Kashmir). This subspecies is characterized by a larger body size, with wing lengths ranging from 425–460 mm in males and 430–495 mm in females, and weights from 590–1,280 g in males and 945–1,760 g in females; its tends to be darker and more uniformly on the underparts, with juveniles showing chequered patterns on the upperparts. In contrast, B. r. cirtensis (also known as the Atlas long-legged buzzard) is smaller and more compact, with wing lengths of 345–395 mm in males and 380–425 mm in females, approaching the size of some (B. buteo) individuals in certain populations. Its plumage is generally paler and more variable, ranging from nearly all-brown to ghostly white adults, often featuring an orange "tail-ring" and scaled upperwing coverts, with about 30% of individuals displaying a subterminal tail band similar to the steppe buzzard (B. buteo vulpinus). This subspecies is distributed across from northwestern to , with possible extension into Arabia, and has recently been recorded breeding in southern near the and on Italy's Island. There has been debate regarding additional subspecies, such as B. r. bannermani from the Islands, which was historically proposed as a variant of the long-legged buzzard based on morphological similarities like long legs and certain traits. However, it is now often synonymized with the complex ( buteo bannermani) or treated as a distinct species due to genetic and vocal differences, reflecting ongoing taxonomic uncertainty in island populations. Textual descriptions indicate B. r. bannermani's range is restricted to the archipelago, with no confirmed overlap with mainland rufinus or cirtensis distributions. Recent genetic analyses provide evidence supporting the validity of these subspecies while highlighting potential revisions. A post-2010 mitochondrial DNA (mtDNA) study by Jowers et al. (2019) analyzed cytochrome b sequences and found B. r. rufinus forming a distinct clade separate from other Buteo species, confirming its isolation. In contrast, B. r. cirtensis clustered closely with B. buteo subspecies (including buteo and vulpinus), indicating ancient hybridization and gene flow over thousands of years, as evidenced by introgressed museum specimens from Algeria and Tunisia. This suggests cirtensis may warrant reclassification as an allospecies within the common buzzard superspecies rather than a true subspecies of the long-legged buzzard, though morphological distinctions persist.

Description

Size and morphology

The Long-legged buzzard (Buteo rufinus) measures 50–66 cm in total length, with a of 113–160 cm. Adults typically weigh 900–1,600 g, though ranges vary slightly by , with B. r. rufinus males averaging 590–1,280 g and females 945–1,760 g. The species exhibits pronounced sexual size dimorphism typical of raptors, with females 15% larger in linear dimensions and up to 30% heavier than males. Morphologically, it possesses notably long legs relative to other Buteo species such as the (B. buteo), broad wings suited for efficient soaring, a short , and a robust build that supports its aerial hunting lifestyle.

Plumage variation

The Long-legged buzzard ( rufinus) displays considerable polymorphism, with three to four main color morphs: pale (characterized by white or creamy underparts), intermediate (with streaked or mottled underparts), (featuring reddish-brown tones overall), and dark (uniformly dark brown with minimal contrast). The pale morph typically shows a plain pale head and underparts contrasting with darker upperparts and a belly patch, while the morph exhibits rich orange-brown across the body and wings; the dark morph, though rarer, lacks the pale contrasts and appears more uniformly sooty. All morphs share diagnostic features such as dark carpal patches on the underwing and a relatively plain with subtle barring. Juveniles possess a more uniform plumage lacking the adults' bold contrasts, with fine, dense streaking on the pale underparts, an orange tinge on the upperparts, and a featuring 8–11 narrow bars. After the first post-juvenile molt, birds transition to adult-like , developing richer tones, a scaled pattern on the upperwing coverts, and a more prominent orange terminal band on the ; the also darkens from pale in juveniles to in adults. This maturation process typically occurs by the second or third calendar year, with full adult coloration achieved progressively. Geographic variation influences morph frequency, with the pale or brown-type morph more prevalent in arid regions such as the and , where it aids against sandy substrates. In contrast, morphs appear more common in mesic habitats across the nominate ' range in . differences affect morph prevalence, with B. r. cirtensis in favoring brown-type plumages over the more variable and dark forms seen in B. r. rufinus. Molting follows an annual cycle starting post-breeding, generally from May to in resident populations, though timing shifts earlier (e.g., ) in Saharan habitats and later (e.g., ) in mountainous areas. Primaries are replaced sequentially from the innermost outward, with some juveniles undertaking a complete primary molt in their first year, resulting in fresher wing feathers by the third year. This pattern aligns with other *, ensuring flight during the non-breeding period.

Identification features

The long-legged buzzard (Buteo rufinus) is a large distinguished in the field by several prominent visual features. It exhibits dark carpal patches on the underwing, which appear as bold black marks at the wing bend, visible during flight or when perched. The bird's notably long, unfeathered legs are often extended beyond the tail in flight, providing a key structural cue. Its broad wings feature fingered primaries, creating a spread-out hand-like tip that aids in soaring. In flight, the long-legged buzzard adopts a soaring reminiscent of a small , with long wings held in a shallow V-shape and frequent glides. The underwing pattern typically shows a pale base contrasting with darker tips and trailing edges, particularly in light-morph individuals, while darker morphs display more uniform dusky tones but retain the carpal patches. This silhouette, combined with its overall bulkier build compared to smaller hawks, helps separate it from slimmer raptors at distance. Identification challenges arise with similar buzzards and eagles. Compared to the steppe buzzard (Buteo buteo vulpinus), the long-legged buzzard is larger with proportionally longer wings and legs, lacking the steppe form's shorter tarsus and more rounded wingtips; underwing coverts in the long-legged are also more uniformly pale at the base. It differs from the long-legged eagle, likely referring to the (Hieraaetus pennatus) in some contexts, by its bulkier body, broader wings without the eagle's sharper, more pointed primaries, and presence of dark carpal patches absent in the slimmer eagle. Against the (Buteo lagopus), the long-legged lacks feathering on the legs, shows less contrast in underwing markings, and has a tail with subtler banding rather than the rough-legged's prominent dark terminal band. Juveniles can be separated from adults primarily by tail and wing details. Young birds feature more pronounced barring on the , often with three to four narrow bands, compared to the adults' narrower subterminal band or uniform rufous tone. Additionally, juveniles lack the adults' bold black trailing edge on the s, instead showing diffuse dusky fringes that fade with age. These differences are most evident in perched or close views, though overall structure remains similar across ages.

Vocalizations

The long-legged buzzard ( rufinus) produces a variety of vocalizations, though it is generally less vocal overall compared to closely related species like the (B. buteo). The primary call is a loud, plaintive scream, often transcribed as "kyaaah," lasting approximately 0.5–0.8 seconds and typically dropping in pitch with a wavering quality. This call is frequently uttered during flight, particularly while soaring, and serves functions such as territorial defense and . Acoustically, the species' calls feature notes with inter-note intervals of about 3.5 seconds, a frequency range of 1–4 kHz, and emphasis around 2.0 kHz, often exhibiting a wavering structure. These vocalizations are given in contexts such as perched interactions or near the nest, including alarm calls when threats approach sites. The calls of the long-legged buzzard are very similar to those of the , with sound recordings showing overlapping characteristics in note structure and frequency, though the long-legged buzzard's notes may appear slightly longer and more drawn out in some instances. Variations occur by context, such as sharper alarm notes for threats and softer contact calls between pairs, while juveniles produce calls distinct from adult vocalizations.

Distribution and habitat

Geographic range

The long-legged buzzard (Buteo rufinus) breeds across a wide expanse of the , primarily in arid and semi-arid regions of the Palearctic. Its core breeding range extends from southeastern Europe, including the (such as , , and ), through the (, , and the ), (, , and ), to northwestern and northwestern . In , breeding occurs from eastward to . The nominate subspecies B. r. rufinus occupies much of this Eurasian and Middle Eastern territory, while the North African subspecies B. r. cirtensis is distributed from northwest to , with possible breeding in parts of Arabia. Southern populations, such as those in , are largely resident year-round. The species' distribution has expanded in in recent decades, with confirmed breeding in southern near the and on Italy's Island since the early 2000s, alongside population growth in and colonization of starting in the 1990s. In , the breeding population increased from 34 occupied territories in 2005 to 115 in 2021. The European population trend is increasing, largely due to northward range expansion. The long-legged buzzard inhabits elevations from to 3,500 m in mountainous areas.

Habitat preferences

The long-legged buzzard (Buteo rufinus) primarily inhabits open, arid landscapes across its range, favoring steppes, semi-deserts, and dry grasslands where visibility for hunting is optimal. It avoids dense forests and thrives in environments with sparse vegetation, including hilly plains, open meadows, and coastal cliffs, often at elevations up to 3,500 meters. These preferences align with its distribution in southeastern Europe, central Asia, and parts of , where such habitats predominate. For nesting, the selects elevated sites such as cliffs, rocky outcrops, and crags, typically 2–30 meters above ground, providing protection and vantage points. In some regions, it occasionally uses trees, shrubs, or human-made structures like old buildings when natural cliffs are unavailable, demonstrating flexibility in site selection. Foraging occurs predominantly in flat or gently sloping open plains with low cover, enabling the to spot and pursue ground-dwelling prey effectively. It frequently perches on elevated features like power poles or dead trees in these areas to scan for small mammals. The species shows notable adaptability to human-altered environments, utilizing agricultural fields and croplands for hunting, and even benefiting from conversion to farmland in certain areas. This tolerance allows it to persist near human settlements, including village outskirts.

Migration

Patterns and timing

The long-legged buzzard (Buteo rufinus) displays varied migratory behaviors depending on and geographic location. The nominate (B. r. rufinus) is partially migratory, with northern and eastern populations undertaking southward movements in winter while southern populations remain largely sedentary. In contrast, the North (B. r. cirtensis) is mostly , with only occasional dispersal by individuals. These differences reflect adaptations to regional climates, as detailed in the taxonomy section. Autumn migration for migratory populations typically occurs from late to , with birds departing breeding grounds primarily in September and October. Spring return migration takes place between March and May, often peaking in April. Juveniles generally migrate later than adults in both seasons, extending the overall period of movement. Populations in milder climates, such as those in , exhibit sedentary tendencies year-round, avoiding the need for long-distance travel. is influenced by environmental factors including weather conditions and food availability, with prey abundance—such as —prompting movements when resources decline in northern areas during winter.

Routes and wintering grounds

The long-legged buzzard (Buteo rufinus) undertakes long-distance migration primarily along north-south corridors through the , with key overland crossings at the Strait in and sea straits in the region, such as the and . Populations breeding in southeastern Europe, Turkey, and follow these pathways southward, funneling through bottlenecks like the eastern coast near , , and the , where concentrations of thousands can occur during peak passage in autumn. Wintering grounds are concentrated in the southern (including southern , , and Arabia), the ( and ), and parts of (such as and ), where birds exploit open arid and semi-arid habitats from October to March. Notable aggregations form at sites like the region, supporting up to several thousand individuals during non-breeding periods. Some populations, particularly in the Judean foothills of , exhibit a rare reverse pattern, moving northward to winter in , , and instead. Important stopover sites include coastal wetlands and river valleys for resting and refueling, such as the in , where birds pause during southward journeys to utilize rich foraging areas amid the marshes. Satellite tracking studies from the 2010s, involving GPS-tagged individuals from breeding areas in and , reveal average migration distances of 2,000–5,000 km, with outbound flights covering these spans in 3–5 days at speeds of 12–13 m/s, though routes vary by population and year. These movements align with the species' autumn departure from to and spring return in to .

Diet and foraging

Prey items

The long-legged buzzard ( rufinus) has an opportunistic diet dominated by small mammals, which typically comprise 60-70% of prey items by frequency across various studies, though this varies regionally with habitat availability. Examples include voles (Microtus arvalis and M. subarvalis), gerbils, the (Rhombomys opimus), black rats (Rattus rattus), house mice ( musculus), Persian squirrels ( anomalus), long-eared hedgehogs (Hemiechinus auritus), and weasels (Mustela nivalis). Reptiles form a significant secondary component, for 15-56% of the diet by frequency, with higher proportions in arid or desert regions such as southwestern and . Common species include agamid such as the starred agama (Stellagama stellio), brilliant ground agama (Trapelus agilis), and large-scaled rock agama (Laudakia nupta), as well as green (Lacerta viridis) and like the large whip snake (Dolichophis jugularis). Birds represent a smaller portion, around 4-18% of prey items, including species such as (Turdus merula) and Isabelline (Oenanthe isabellina). Insects and amphibians are taken occasionally, comprising up to 10% of the diet by frequency but negligible , with no specific species frequently documented. Carrion is consumed opportunistically but is not a primary food source. Dietary composition shows regional variations, with mammals dominating in steppe and forested areas like and northwestern China, while reptiles prevail in desert habitats of and . Prey items generally range from 50-500 g in mass, selected for ease of capture, with a mean around 167 g in Mediterranean populations.
Prey CategoryFrequency (%)Biomass (%)Example Regions
Small Mammals60-7040-60Bulgaria, China, Cyprus
Reptiles15-5635-57Iran, Jordan, Cyprus
Birds4-182-5Iran, Cyprus
Insects/Other<10<1Cyprus, general

Hunting methods

The Long-legged buzzard primarily employs still-hunting techniques from elevated perches, such as power poles, rock outcrops, or dead trees, where it scans the ground for prey before executing a rapid pounce or short glide to capture it. In open habitats like steppes and fields, it also soars or hovers at low to moderate heights, typically up to 30 meters, using its acute vision to spot movement below and then stooping steeply to seize prey such as small mammals or reptiles. These aerial pursuits are efficient for covering large areas, allowing the bird to exploit diurnal ground-dwelling species during periods of high activity. On occasion, the long-legged buzzard forages terrestrially, standing or walking on its notably long legs to stalk or ambush prey near burrows, particularly targeting reptiles and in arid or semi-arid environments. This ground-based approach leverages its physical adaptations for navigating uneven and pursuing evasive targets over short distances. The species opportunistically scavenges carrion, including and remains, especially in non-breeding seasons or disturbed areas, supplementing its active hunting when prey is scarce. As a diurnal hunter, the long-legged buzzard is most active during daylight hours, with intensity peaking in the early morning and late afternoon, aligning with optimal visibility and prey availability.

Interspecific relationships

The long-legged buzzard (Buteo rufinus) exhibits significant with sympatric raptors, particularly in and nesting resources, which shapes its distribution and behavior in shared habitats. In regions like , its diet overlaps moderately with that of the ( fasciata), with both species targeting small mammals such as black rats (Rattus rattus), though the buzzard's prey biomass averages 167 g per item compared to 350 g for the , and Pianka's overlap index remains below 0.5, suggesting niche partitioning mitigates intense competition. Similarly, in the Judean Foothills of , the long-legged buzzard coexists with the short-toed (Circaetus gallicus) through multidimensional differentiation: the buzzard forages closer to nests (mean 2.35 km) in low natural vegetation, while the travels farther (13.03 km) and prefers cultivated fields, reducing direct resource conflicts despite high nest densities. In , with golden ( chrysaetos) influences nesting site selection, with buzzard nests on rock faces or cliffs showing little spatial overlap with territories, likely due to territorial disputes over suitable breeding areas. As a predator, the long-legged buzzard occasionally preys on avian species, contributing to interactions with ground-nesting birds. Birds constitute a small but consistent portion of its diet (4.3% by frequency in Cyprus, 1.8% in Jordan), potentially including vulnerable nestlings during breeding seasons when opportunistic hunting occurs in open habitats. Larger raptors, such as steppe eagles (Aquila nipalensis), exert pressure through kleptoparasitism or predation attempts on buzzards, as observed in similar interactions where steppe eagles pursue and steal from or attack smaller buzzards during migration, though direct cases with long-legged buzzards are less documented. The species benefits from symbiotic relationships in human-modified landscapes, particularly agricultural areas where populations thrive as s. In , the abundance of black rats—reaching levels in wet years and damaging crops—provides a reliable source, with mammals comprising 68.8% of the buzzard's by frequency, allowing it to exploit these environments without direct conflict. As a top predator in ecosystems, the long-legged buzzard plays a key role in maintenance by controlling prey populations, such as and small mammals, which helps regulate balance and prevents or pest outbreaks in arid grasslands.

Breeding

Courtship and nesting

The long-legged buzzard forms monogamous pairs that often persist across multiple breeding seasons, with evidence suggesting the same individuals return to territories year after year. Pair bonding is reinforced through mutual activities such as branch carrying and copulations observed during the early breeding period. Courtship typically commences in late February to March, involving aerial displays where pairs engage in mutual soaring, calling flights, and chases to advertise occupancy and strengthen bonds. These behaviors help in selection and establishment, with resident populations defending areas year-round. Territories average 6.9 km² in extent, ranging from 3 to 14 km², providing ample space for and nesting in open habitats. Nests are constructed on cliff ledges or in , often in elevated positions such as precipices or patches near open ground, and are frequently reused over successive years with multiple alternate sites per (averaging 1.8 nests). involves a platform of sticks less than 2.5 cm in diameter, measuring about 71 cm in diameter and 13 cm high, lined with softer materials like , , and ; fresh greenery such as leafy branches is added periodically, particularly before egg-laying. In regions with limited cliffs, such as forested areas, nests adapt to sites while maintaining similar structure.

Eggs, incubation, and parental care

The female long-legged buzzard lays a clutch of 2–4 eggs, typically at intervals of 2–3 days, with the eggs being off-white and marked with red-brown spots or blotches. Clutch sizes average 2.7–3.3 eggs across studied populations, though variation occurs regionally. Incubation begins with the laying of the penultimate and lasts 28–34 days, with the female performing the majority of the duties while the male forages and delivers prey to the nest to sustain her. The male occasionally relieves the female briefly, but her near-constant attendance ensures warmth during this period. Upon , the semi-altricial emerge covered in white to creamy-white down, with asynchronous hatching intervals of 29–44 hours that promote competition for and often result in to 1–2 survivors per nest. Both parents share chick-rearing responsibilities, with the brooding the young initially while the supplies most prey; as the chicks grow, the increasingly participates in . The nestlings at 40–50 days old, typically around 49–50 days in observed cases, after which parental provisioning continues for several weeks until independence. Breeding success yields 0.5–1.5 fledglings per breeding pair annually, varying by habitat quality and region—for instance, 0.7 in and 0.93 in northeastern —with higher rates in successful nests averaging 1.4–2.3 young. Nestling survival is generally high at 80–90% from to fledging in monitored populations.

Conservation status

The global of the long-legged buzzard (Buteo rufinus) is estimated at 100,000–499,999 mature individuals, with the trend suspected to be stable as of 2021 and no significant changes reported through 2025. In , the is estimated at 13,800–22,900 pairs, representing approximately 17% of the global and equivalent to 27,600–45,800 mature individuals; this regional has shown a slight increase, accompanied by northward expansion. Recent studies (as of 2024) confirm ongoing increases, with Romania's rising to 400–900 pairs by 2022, contributing to further northward expansion across . Populations in remain stable, while those in exhibit variability, with notable declines in northern regions. Overall, the species experiences local fluctuations, increases, and declines, but the global trend is stable; for instance, the Arabian subpopulation has declined by approximately 5% over a recent 10-year period, linked to habitat changes in fragmented areas. In northern , ongoing declines have been documented, contrasting with stability or growth in core Eurasian breeding grounds. Population monitoring relies primarily on systematic breeding pair surveys conducted in key countries, such as those detailed in multi-nation assessments, alongside migration counts at ecological bottlenecks to track annual movements and abundance. These methods provide essential data for detecting local variations, though global estimates remain of poor quality due to challenges in surveying vast Asian and ranges.

Threats and challenges

The Long-legged buzzard (Buteo rufinus) faces significant threats from habitat loss, primarily driven by agricultural intensification and , which degrade its preferred open , semi-desert, and arid habitats across and . Conversion of natural landscapes to reduces availability of prey such as small mammals and insects, while the expansion of orchards and vineyards in regions like has led to localized declines. In the , habitat loss has contributed to an estimated 5% population decrease over a decade. Persecution through shooting and poisoning poses a major direct threat, particularly in and the . In , over 70% of examined long-legged buzzards admitted to rehabilitation centers between 1996 and 2005 had been shot, indicating persecution as the leading cause of mortality. In , shooting, disturbance at nest sites, and secondary poisoning from baits targeted at predators like red foxes (e.g., poisoned goat carcasses) remain primary risks. Historical pesticide poisoning in during the 1950s affected the species, though populations have since recovered, but illegal trade in live birds persists in markets in , , and . Electrocution on power lines and collisions with wind farms during migration further endanger the species, especially as energy infrastructure expands. Fatal electrocutions have been documented across its range, with vulnerable individuals perching on poorly designed poles in open habitats. The long-legged buzzard is classified as highly vulnerable to wind turbine collisions due to its soaring flight behavior along migration routes in the Mediterranean and , with risks intensifying post-2020 amid rapid wind farm development. Climate change exacerbates these pressures by altering patterns and regimes, potentially disrupting prey distribution and breeding success in . The species shows high sensitivity to variables like during the warmest period and seasonality, contributing to range shifts but also heightened vulnerability in northern populations (e.g., , ). In its range, particularly the , overgrazing by livestock degrades habitats alongside wood harvesting and burning, threatening wintering populations. These combined factors have led to unfavorable in parts of its range, underscoring the need to address cumulative impacts on population persistence.

Conservation efforts

The long-legged buzzard receives legal protection through its inclusion on Appendix II of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (), which controls international trade to avoid impacts on wild populations. In European range states, the is listed under Annex I of the EU Birds Directive, mandating strict protection, habitat safeguards, and the establishment of Special Protection Areas to support its conservation. It is also covered by Appendix II of the Convention on the Conservation of Migratory Species of Wild Animals () and Category 3 of the Raptors , promoting coordinated international actions for migratory raptors. Key initiatives focus on monitoring and habitat management to bolster populations. Systematic breeding surveys occur in countries like , , , and , while counts at bottlenecks such as those in and track annual movements and inform protection strategies, supported by organizations including and the Peregrine Fund. In habitats, restoration projects emphasize grassland rehabilitation and prey enhancement, as seen in Ukraine's region, where efforts to reverse agricultural degradation have facilitated species resettlement by improving conditions. Anti-poisoning campaigns in the have driven notable recoveries among , including the long-legged buzzard, by targeting illegal baiting that affects and predators alike. In , these measures, combined with protections, contributed to a substantial increase from low numbers in the late to 700–1,000 breeding pairs by 2020. Educational programs in , using the species as a flagship for awareness, have further enhanced community involvement and reduced through school-based modeling. Ongoing recommendations emphasize mitigating human-induced risks to sustain gains. modifications, such as insulating poles and rerouting in areas, are prioritized to curb electrocution, drawing from successful trials in raptor-heavy regions like that reduced incidents by over 90% at treated sites. Reduced in agricultural and Sahelian zones is advised to limit in prey, protecting the species from secondary poisoning as highlighted in vulnerability assessments.

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