Species names in all available languages
Language | Common name |
---|---|
Afrikaans | Europese Aasvoël |
Albanian | Shkaba |
Arabic | نسر اسمر اوراسي |
Armenian | Սպիտակագլուխ անգղ |
Asturian | Utre comñn |
Azerbaijani | Ağbaş kərkəs |
Basque | Sai arrea |
Bulgarian | Белоглав лешояд |
Catalan | voltor comú |
Chinese (SIM) | 兀鹫 |
Croatian | bjeloglavi sup |
Czech | sup bělohlavý |
Danish | Gåsegrib |
Dutch | Vale Gier |
English | Eurasian Griffon |
English (India) | Eurasian Griffon (Griffon Vulture) |
English (Kenya) | Eurasian Griffon Vulture |
English (UK) | Griffon Vulture |
English (United States) | Eurasian Griffon |
Finnish | hanhikorppikotka |
French | Vautour fauve |
French (France) | Vautour fauve |
Galician | Voitre común |
German | Gänsegeier |
Greek | Όρνιο |
Hebrew | נשר מקראי |
Hungarian | Fakó keselyű |
Icelandic | Gæsagammur |
Italian | Grifone |
Japanese | シロエリハゲワシ |
Latvian | Baltgalvas grifs |
Lithuanian | Palšasis grifas |
Malayalam | ജടായു |
Mongolian | Ухаа хажир |
Norwegian | gåsegribb |
Persian | دال معمولی |
Polish | sęp płowy |
Portuguese (Portugal) | Grifo-comum |
Romanian | Vultur sur |
Russian | Белоголовый сип |
Serbian | Beloglavi sup |
Slovak | sup bielohlavý |
Slovenian | Beloglavi jastreb |
Spanish | Buitre Leonado |
Spanish (Spain) | Buitre leonado |
Swedish | gåsgam |
Turkish | Kızıl Akbaba |
Ukrainian | Сип білоголовий |
Revision Notes
Alfredo Salvador evaluated and updated the entire account, as possible.
Gyps fulvus (Hablizl, 1783)
Definitions
- GYPS
- gyps
- fulvum / fulvus
The Key to Scientific Names
Legend Overview
Eurasian Griffon Gyps fulvus Scientific name definitions
Version: 6.0 — Published July 26, 2024
Diet and Foraging
Introduction
The Eurasian Griffon is an obligate scavenger that feeds on carcasses, mostly of domestic or wild ungulates; only occasionally will it kill an animal as prey. It depends on thermal updrafts for flight, and is most active when hungry, flying greater distances and moving farther from the roost than when it is satiated. To avoid starvation, it changes its strategy based on how many days it has gone without food. For the first few days without food, to increase its chances of finding food it travels farther, increasing its maximal displacement, and flying at higher altitudes. In the days that follow, it minimizes energy expenditure by decreasing these three measures. The Eurasian Griffon can survive periods of food deprivation of at least 31 consecutive days. It forages in loose groups and is drawn to a foraging site by other vultures that have located food, as indicated by a change in their flight style. When a bird locates food, it will soar low then descend vertically to the carcass flapping its wings with its feet hanging down. At the carcass, the Eurasian Griffon follows a despotic dominance hierarchy that lends priority to adults over subadults and juveniles, and individuals fight to keep positions close to the carcass and to defend pieces of food. It can also receive information about the location of carrion in communal roosts.
Feeding
Main Foods Taken
The Eurasian Griffon mainly feeds on carcasses (typically ungulates) abandoned by predators, domestic or wild animals killed by disease or accident, livestock carcasses deposited on dunghills, food stolen from other species, and occasionally animals it has killed itself (272). Consumption of stranded carcasses along the sea coast was recorded near Oriñón, Cantabria (Spain; 273) and on Cres Island (Croatia; 85). In the Eastern Rhodope Mountains (Bulgaria and Greece), 60.2% of the its diet was animals killed by predators (gray wolf [Canis lupus], golden jackal [Canis aureus], and feral dogs), 37.6% that died of natural causes, and 2.2% by poaching (n = 93; 274). In Gir National Park (India), 45.87% of recorded carcasses had died of natural causes and 54.12% by predation of other animals (n = 194; 215).
Movements to follow cattle drives, both in fall and spring, were observed in Tajikistan, Kazakhstan, and Turkmenistan (156). In the Sierras de Cazorla, Segura y Las Villas Natural Park (southeastern Spain), 63% of GPS tracked Eurasian Griffon (n = 30), mainly non-breeding birds and females, increased foraging activity in the pasturelands occupied by transhumant herds of domestic ungulates from June–November (275).
The saiga antelope (Saiga tatarica), a once-abundant migratory species of the Eurasian Steppe, is now endangered, in part because of its susceptibility to disease; in west-central Kazakhstan, groups of Eurasian Griffon and Cinereous Vulture (Aegypius monachus) were observed during July and August 1958 at several locations in association with the beginning of a mass epizootic mortality event in saiga antelope herds. On 21 August, Eurasian Griffons were observed in one of these herds of sick saigas; the birds were sitting on the ground at a distance, waiting for the infected animals to die (115).
In June 2003, three Eurasian Griffon were recorded in the Netherlands preying upon 28 White Stork (Ciconia ciconia) nestlings aged 2–8 weeks from a total of 18 nests, from the De Lokkerij breeding colony (6 nests) and ten other sites located 0.1–8.2 km away (276).
Microhabitats for Foraging
Foraging Eurasian Griffon in Spain showed a preference for areas with natural and semi-natural vegetation (277). On Crete (Greece), it foraged mainly over open areas with bare rocks and Mediterranean scrubland (278). In Kazakhstan, it avoided forested areas and river valleys, preferring instead to forage over highland and lowland steppe and, less often, in deserts (115). It selects foraging habitat in response to the spatial and temporal distribution of food; on Crete and in Kazakhstan, it foraged in lower areas during winter and shifted to higher habitat during summer (201, 279; Katzner, personal communication).
Foraging locations (n = 24,302) recorded from 60 GPS-tracked birds in Spain between 2014–2016 were concentrated in agroforestry areas, areas with higher livestock density, natural grasslands, transitional woodland-shrub, sclerophyllous vegetation, and broad-leaved forests. It tended to avoid, or forage less often, in non-irrigated arable land, permanent irrigated land, and olive groves (277).
The use of different foraging microhabitats seems to depend on the abundance of carcasses in the wild. Birds will also use supplemental feeding stations; such supplemental feeding stations were established to compensate for the scarcity of carrion in the wild and thus contribute to the recovery of populations (see Management). In the Grands Causses (France), GPS-tracked adult birds selected feeding stations more often than they did other habitats throughout the year. In one study, adults showed a preference in spring and summer for small, unpredictable feeding stations rather than large, highly predictable ones; preference for small feeding stations could be related to an attempt to reduce intraspecific competition. Open habitats were also selected; forested areas and urbanized areas were avoided (280). Most feeding events (71.4%) of 47 GPS-tracked individuals in Israel and Jordan occurred at a feeding station, but the birds also searched for food elsewhere (281).
In the Eastern Rhodopes Mountains (Bulgaria and Greece), most feeding events of 11 GPS-tracked birds occurred at carcasses of free-range livestock and game found in the wild (77.4%), and only 22.6% were at feeding stations (n = 1,036). However, there was seasonal variation: 56.5% ± 16.1 SD of the feeding events in winter were at feeding stations, decreasing to 30.4% ± 10 SD in spring, 19.82% ± 7.8 SD in summer, and 29.56% ± 11.4 SD in autumn. Higher use of feeding stations was observed in breeding birds during the pre-breeding period and during incubation. In addition to seasonal differences, birds would also use supplemental feeding stations during periods of bad weather when flight was difficult, such as during periods of rain or high wind, while they would use carrion at wild sites during warm weather (282).
Food Capture and Consumption
Like other species of the genus Gyps, the Eurasian Griffon is considered a gulper, a mode of feeding by which they swallow large chunks of soft tissues from the carcasses (283), with unique features to its bill, skull, and mandible that are adapted to feed on the muscle and viscera of carrion (283, 284, 285, 286). Specifically, the skull and first two vertebrae of the Eurasian Griffon are long and narrow, with specializations in the morphology of the atlas-axis complex and the neck musculature that allow it to adopt specific postures while feeding (287). Typical feeding behavior includes pulling with the bill, inserting the head through an opening, tearing skin, and tugging out fibers (284).
The number and speed of feeding pecks at carcasses differs among species, with some having similar feeding rates. In comparison with other Spanish scavengers, the Eurasian Griffon is a balanced scavenger, as compared to the Cinereous Vulture (Aegypius monachus) and Common Raven (Corvus corax), which will peck only a few times over a moderate time; in the Eurasian Griffon, the mean number of feeding pecks was 5.7 pecks/min ± 0.9 SD (n = 72) in adults, and 4.9 pecks/min ± 0.4 SD (n = 128) in non-adults (288).
Visual acuity in Gyps vultures is high in comparison to most other raptors (289); the Eurasian Griffon, as an active forager, uses sight to search for carrion. One individual's visual acuity measured an estimated 104 cycles per degree of visual angle, i.e., it had the ability to distinguish 104 black and 104 white vertical bars in one degree of visual angle (290). The Eurasian Griffon's field of vision contains a small binocular region (21º) and blind areas above, below, and behind the head (291). Average flight altitude was 462 m in Israel and 338 m in France (267).
The Eurasian Griffon forages in loose groups to locate large carcasses of ungulates (292). A breeding pair will take turns foraging while the other remains on the nest; however, it is unknown whether the foraging member searches for food alone or whether it joins an existing group to feed. The mean number of daylight hours that passed between when an animal died and when the Eurasian Griffon began feeding on the carcass was 30.76 h ± 11.38 SD in the Caucasus (194), but a carcass was found in as little as two hours in one instance in Extremadura (Spain; 293). In the Spanish Pyrenees, carcasses were detected mainly by Eurasian Griffon, faster in open landscapes (15.4 h ± 19.17 SD) than in shrublands (24.56 h ± 37.34 SD; 294).
Foraging Eurasian Griffon learn the location of carrion by following other individuals that may be flying toward a carcass or by noticing where other vultures sink vertically to the ground (1, 295). On Crete (Greece), individuals that had located food (n = 23) either soared low to the ground or—with dangling feet or flapping flight—sank vertically to the carcass (278). Another method of learning the location of carrion takes place at communal roosts (17): a Eurasian Griffon that has fed on a carcass, upon returning to the roost to sleep, provides information to other vultures. The mechanism of information transfer is unknown, but it is likely based on visual cues such as bloody plumage, a full crop, or a particular flight behavior (296). Some vultures that fed on carrion (38%) returned to the site the next day, and often another individual followed immediately (within 2 min) and at close range (1.61 km ± 0.83 SD; 296).
In addition to reliance on conspecifics, the unpredictable availability of carrion in the wild can facilitate interspecific interactions. The Eurasian Griffon located wild carrion quicker when small scavenger species were already present at a feeding site, and small scavengers were able to feed successfully once the Eurasian Griffon dismembered the carrion. This mutual benefit was not observed at supplemental feeding stations, where the Eurasian Griffon arrived earlier and, by their sheer numbers, excluded smaller scavengers from this predictable food source (297). It can also receive benefits from other large scavengers; in Gir National Park (India), carcasses consumed by the White-rumped Vulture (Gyps bengalensis), Indian Vulture (Gyps indicus), and Eurasian Griffon had either been opened by lions, leopards, hyenas, jackals, or by humans (215).
Foraging distances of the Eurasian Griffon from several populations (French Pyrenees, Ebro valley, Sierra de Cazorla, Cataluña, and Cádiz province) usually were (92.1%) < 350 km from the nest or activity center (n = 106 tracked birds); however, foraging movements of 32 of those individuals were recorded as far as 800 km, at open oak habitats of southwestern Iberia. Long distance movements were mostly carried out by females in summer (298). Several studies indicate that the distance traveled while foraging appears to be related to the abundance of carrion in the wild. The mean distance flown daily by foraging birds was 160 km in Israel and 141 km in France (267). In the Eastern Rhodope Mountains (Bulgaria and Greece), on average, 11 GPS-tracked immature birds traveled longer distances on days they fed on carcasses in the wild (96.7 km ± 57.4 SD) than on days they fed at feeding stations (70.6 km ± 59.7 SD) or on days with no recorded feeding (70.8 km ± 59.8 SD; 282).
The Eurasian Griffon can endure a varying number of days between feedings. One study of GPS-tracked birds conducted in Israel reported periods of 7–10 d between successive feedings (299), while another study in Israel reported that birds fed approximately every three days (281). In the Eastern Rhodopes (Bulgaria and Greece), it attended feeding events every 1.6 d on average, decreasing the number of visits to every 4.1 d in January and February (282). The food deprivation period in the wild can be longer; in a tracked Eurasian Griffon breeding pair, the male underwent a continuous incubation period of 31 d after loss of the female. Tracking data showed that the vulture survived this starvation event (300). In a nest in southern Spain, the male was shot dead on the day 30 of incubation; from that day, the female incubated for 28 uninterrupted days until the chick hatched. Two days later, the chick was found dead and the female was observed flying from the nest (301).
The Eurasian Griffon is also most active when hungry; it flies greater distances and moves farther from the roost when hungry than when it is satiated. To avoid starvation, it will change its foraging strategy based on how many days it has gone without food. For the first few days without food, it will travel farther, increase its maximal displacement (Euclidean distance between the initial and farthest location of the day), and fly at a higher altitudes to increase its chances of finding food. In the days that follow, these three measures decrease, indicating the adoption of a strategy that minimizes energy expenditure. Spiegel et al. (281) found that birds usually made one or two stops per day, rarely more than four, before returning to the evening roost. In Bizkaia (Spain), 24 experimental feeding sites were established in an area of 10,614 km2 to analyze the foraging movements of banded Eurasian Griffon (n = 241). Rather than moving randomly throughout the entire study area, adults congregated at three separate core feeding areas; subadults exhibited the same behavior, once they had become established in the breeding colony. The study suggested that this species restricts its foraging to areas close to its breeding site (302).
The highest number of individuals observed near carrion was 146 in the Pyrenees Mountains (France; 200), and more than 300 in Spain (272). Congregations of ca. 1,000 birds were observed at feeding sites in Segovia (Spain; 303). In a feeding group, an individual gains access to carrion based on its age, fighting ability, and hunger level (304, 296, 305). A field study in southern Israel with tracked birds found that the time to initiate feeding was negatively associated with age and with hunger level, and positively associated with arrival time (n = 62; 296). In France, older adults arrived at carcasses first and departed before other age-classes arrived. The mean duration of stay at carcasses was 5.2 min ± 12.7 SD in old adults, 13.9 min ± 15.5 SD in young adults, and 29.5 min ± 44.8 SD in immatures (304). In Spain, adults remained at carcasses for a mean of 17.6 min ± 3.7 SD (n = 72), and non-adults for 26.7 min ± 4.0 SD (n = 128), feeding for 6.3 min ± 1.2 SD and 9.5 min ± 1.4 SD, respectively (288).
Occasionally, birds will spend the night on trees or rocks next to the carcass to continue feeding the next day, as observed in Spain (293) and India (215). At Gir National Park (India), when a carcass was in the open, some vultures continued feeding during moonlit nights (215). In alpine pastures of Somiedo Natural Park (Asturias Region, Spain), at least 14 Eurasian Griffon were recorded by camera traps scavenging a mean of three hours per night at two cow carcasses during five nights in summer. The minimum number of Eurasian Griffon scavenging during the night (mean 4 ± 1 SE) was lower that during the day (mean 8 ± 1 SE). Nocturnal mean temperatures were higher (13.9°C ± 0.6° SE) during scavenging nights than during other nights (8.1°C ± 0.6 SE; 306). In Bulgaria, 19 cases of nocturnal activity on the ground by 1–3 individuals were recorded at Kresna Gorge during 2012–2022. Active feeding was observed in 68.4% of cases (307). In the central Apennines (Italy), nocturnal and crepuscular feeding on a horse carcass was observed (308).
In France, more old adults than young adults and immatures were observed at carrion sites, although in autumn the number of juveniles at a carrion site increased (304). Juvenile vultures preferred to feed at supplementary feeding points located far from the breeding colonies and where less and more irregular carrion is deposited. Juveniles arrived at these sites before adults and in a higher proportion (309). As the group size increased, the feeding rate decreased due to competition and interference (310). During carrion exploitation observations in Spain, birds followed a dominance gradient from adults to subadults and juveniles, fought to keep positions close to the carrion, and defended pieces of food from theft by other vultures (305).
Diet
Major Food Items
In Spain, the Eurasian Griffon feeds on goat, sheep , donkey, cow , Iberian ibex (Capra pyrenaica), Pyrenean chamois (Rupicapra pyrenaica), red deer (Cervus elaphus), horse, domestic pig, wild boar (Sus scrofa), dog, cat, European fallow deer (Dama dama), red fox (Vulpes vulpes), Iberian hare (Lepus granatensis), European rabbit (Oryctolagus cuniculus), and birds (311, 301, 312, 313 , 314, 17, 272, 315). In Germany, feeding at carcasses of cow, pig, and sheep was recorded (148). In Crete (Greece), meals of sheep, goat, rabbit, and beech marten (Martes foina) were recorded (316).
In Armenia, food items include horse, wild goat (Capra aegagrus), and brown bear (Ursus arctos; 317). In Azerbaijan, it feeds on cattle, domestic buffalo, horse, donkey, sheep, goat, dog, cat, red deer, urial (Ovis orientalis), Daghestan tur (Capra cylindricornis), chamois (Rupicapra rupicapra), wild goat, goitered gazelle (Gazella subgutturosa), European roe (Capreolus capreolus), wild boar, saiga antelope (Saiga tatarica), brown bear, gray wolf (Canis lupus), golden jackal (Canis aureus), red fox, European badger (Meles meles), raccoon (Procyon lotor), marbled polecat (Vormela peregusna), beech marten (Martes foina), least weasel (Mustela nivalis), European hare (Lepus europaeus), Indian porcupine (Hystrix indica), spur-thighed tortoise (Testudo graeca), grass snake (Natrix natrix), European glass lizard (Pseudopus apodus), and fish (318, 319). In Kazakhstan, it has been documented feeding on domestic livestock, Siberian roe deer (Capreolus pygargus; 320), Siberian ibex (Capra sibirica), argali (Ovis ammon), goitered gazelle, saiga antelope, and steppe marmot (Marmota bobak; 115). In Turkmenistan, wild goat, urial (Ovis orientalis), Russian tortoise (Testudo horsfieldii), red fox, cow, sheep, horse, camel and donkey were recorded as part of its diet (321). In Cyprus, a Eurasian Griffon fed on a rat (Rattus rattus; 322). In Gir National Park (India), it consumed water buffalo, zebu cattle, camel, horse, chital (Axis axis), nilgai (Boselaphus tragocamelus), sambar (Rusa unicolor), and Indian porcupine (215). In Little Rann of Kachchh (Gujarat, India), a bird was observed feeding on a carcass of wild ass (Equus hemionus; 323). Eurasian Griffon wintering in Gambia were observed feeding at carcasses of donkey, cow, goat, and horse (133). It was also recorded feeding on dead camels (Camelus dromedarius) once near Gebel Abu Hareigal (Egypt; 173).
Eurasian Griffon were recorded feeding on Mallard (Anas platyrhynchos) carcasses in Hungary (324), and Graylag Goose (Anser anser) carcasses in Doñana National Park (Spain; 325). It also occasionally feeds on road-killed animals, such as cats (315) and dogs (326). The ingestion of European mudminnow (Umbra krameri), 5–10 cm in length, thrown away by fishermen, was recorded at the mouth of the Dniester river (Ukraine; 9). The Eurasian Griffon also occasionally feeds on individuals of its own species. There is a record of birds feeding on a dead conspecific (327); in another instance, a Eurasian Griffon whose wing had been trapped by a falling rock was killed and consumed by other individuals (328).
The Eurasian Griffon rarely carries food away from the feeding site. However, in Abkhazia (Georgia) in June, an adult was observed arriving at the nest carrying intestine, probably sheep, in its claws (329). It was also observed in May flying in Cyprus with a rat in its beak (322).
There is evidence that this species benefits from the hunting of wild ungulates, particularly red deer and wild boar. A study conducted in the Cantabrian Mountains (Spain) revealed that the location of roosts within the study area overlapped with hunting sectors containing the highest number of shot red deer and wild boar. Additionally, the birds occupied these roosts during months that coincided with the hunting season (330). Since 2000, however, European Union legislation has progressively limited the abandonment of dead animals. As a result, the Eurasian Griffon has expanded its trophic niche to include significant numbers of rabbits and garbage (331).
Although the Eurasian Griffon is considered an obligate scavenger, it is nonetheless capable of eating very weak animals that are still alive, though it does this rarely (272). For example, Camiña Cardenal et al. (332) observed birds devouring a very weakened, yet live, sheep. In areas of high population density in northern Spain, it also occasionally preys on newborn cattle (see also Conservation and Management). It has also been documented predating White Stork (Ciconia ciconia) nestlings in the Netherlands (276).
While vertebrate carcasses comprise the dominant food items for the species, other items may also be consumed. For example, in Andalucía (Spain), a nestling vomited three small snails (301). There also is a record of birds eating beetles in Andalucía (333; see Quantitative Analysis). In Romania, snails and large insects were found in their crop (179). One source also mentions it feeding on dry grass (9). Pellets of long grass, fibers, and green leaves of the cork tree were found in Cádiz (Spain) near nests and roosts (206); it has been observed eating plants in other situations as well (334; see also Quantitative Analysis). It has also been observed ingesting grit (335); a nestling vomited a piece of grit that was 2.5 cm (301), and one individual had some 7 mm diameter grit in its intestine (336). It also often swallow indigestible fragments of glass, plastic, and metal. These fragments were found in or near the nest and in the stomach of chicks in Israel and Armenia (337). Ceramic fragments were found in food regurgitated by nestlings in the Pyrenees (17).
Calcium, necessary for eggshell formation and bone mineralization, is scarce in the typical diet of soft tissue (338). To compensate for this scarcity in its typical diet, it has been recorded to consuming bone fragments both in captivity and in the wild at Gir National Park (India; 339) and in Spain (293; see also Quantitative Analysis and Social and Interspecific Behavior).
Quantitative Analysis
In Andalucia (Spain), the Eurasian Griffon feeds mainly on goat (34.9%), sheep (20.9%), donkey (11.6%), and cow (7%). To a lesser extent, it also feeds on red deer, horse, and dogs. Birds were also observed occasionally feeding on fallow deer, dromedary camel, fox, and hare (311). In the Sierra Morena mountains (southern Spain), goat and sheep dominated the diet (43.3%), followed by red deer (21.6%), horses (7.5%), cattle (6%), domestic pig (5.2%), and birds (5.2%; 312). Samples of food regurgitated (n = 151) by nestlings (n = 91) in the Pyrenees (Spain) were composed of muscle tissue (43.05%), plants (17.25%), viscera (10%), bones (9.95%), skin (2.65%), cartilage (2%), tendons (1.3%), and snails (1.3%; 17). In Crete (Greece), sheep hair was present in 89.45% of regurgitated pellets, goat hair in 15.5%, rabbit hair in 2.8%, and beech marten hair in 1.4% (n = 142 pellets; 316). In the Eastern Rhodopes (Bulgaria and Greece), the diet was composed mainly of domestic animals (86.9%), including cattle (48.5%), sheep (24.3%), goat (6.6%), horse (3.6%), donkey (2.3%), and dog (1.6%). Wild food items included fallow deer (8.5%), European roe deer (2.3%), red deer (0.7%), wild boar (0.7%), European hare (0.3%), red fox (0.3%), and golden jackal (0.3%, n = 265; 274).
In Turkmenistan, from 1980–2007, records showed a diet of urial (Ovis orientalis, 27.9%), wild goat (Capra aegagrus, 27.1%), sheep (12.9%), Russian tortoise (Testudo horsfieldii, 10.7%), cow (7.1%), goitered gazelle (Gazella subgutturosa, 3.6%), camel (3.6%), onager (Equus hemionus, 2.9%), horse (2.8%), donkey (0.7%), and red fox (0.7%, n = 140; 340). In the central Kopet Dag Mountains (Turkmenistan), wild animals (75.7%) prevailed over domestic cattle (24.3%). Wild goat (32.45%) and urial (32.45%) were the most important items in the diet, while Russian tortoise (9.9%) and red fox (0.9%) were represented in small amounts. Domestic ungulates such as cow (9.0%), sheep (9.0%), horse (3.6%), camel (1.8%), and donkey (0.9%) had lower representation in its diet (n = 111; 321). In Gir National Park (India), domestic livestock represented 92.2% of carcasses recorded and wild animals only 7.2% (n = 194; 218). Domestic livestock included water buffalo (56.70%), zebu cattle (31.95%), camel (3.09%), and horse (1.03%); wild animals were represented by chital (2.57%), nilgai (2.57%), sambar (1.54%), and Indian porcupine (0.51%, n = 194; 215).
In Azerbaijan, the diet showed variation across years that correlated with food availability. In 2008–2009, a large number of sheep were killed by predators, which was reflected by the fact that 60.5% of food items found in nests during that period were sheep (n = 261). The following year (2010), a large number of predators were killed by farmers and pet owners and, consequently, gray wolf (30.8%), golden jackal (27.7%), and red fox (20.0%) represented a higher proportion of food items in the diet of Eurasian Griffon (n = 65). In 2011–2012, the carcasses of 192 horses left illegally became a dominant food source, representing 73.3% of food items (n = 150; 318). In the years 2014–2016, red fox (22–23% of prey items) and golden jackal (19–21% of prey items) were the most important prey of Eurasian Griffon in Azerbaijan (319).
Food Selection and Storage
In Spain, individual Eurasian Griffon were observed feeding most frequently on muscle tissue and viscera of carrion (284, 288 , 17). Another study in Spain observed birds feeding mostly on organs and fleshy parts (nearly 78% of observations), and to a lesser extent on coarse muscle flesh, sinews, and pieces of skin (20% of observations, n = 321; 286). See Diet: Quantitative Analysis.
In GPS-tracked individuals from a population in northern Spain, feeding was based on human-derived resources, whereas in GPS-tracked individuals from a southern population, feeding was based on wild ungulates. In a western Iberian foraging area shared by both populations, in which there are both wild and human-derived resources, individuals preferentially used resources similar to those of their original population, suggesting a cultural component in the diet (341).
Differences in diet between males and females have been observed in Spain. Males consumed more trophic resources of human origin and visited intensive livestock farms and carcass-dumping sites more, while females more frequently visited hunting properties (341).
Nutrition and Energetics
Information needed.
Metabolism and Temperature Regulation
In one study, the resting body temperature had a mean value of 37.7 ºC during the night and 38.9 ºC during the day. Body temperature increased significantly as air temperature increased, whereas metabolic rate did not vary significantly; variation in body temperature independent of metabolic rate may function as a mechanism for saving energy (n = 14; 342). In response to food deprivation over 10.5 d, captive Eurasian Griffon (n = 6) increased body temperature variation, resulting in 4–6 ºC lower body temperature at night, thereby minimizing nocturnal energy expenditure (343).
In warm areas, such as the Mediterranean region, nestlings are unable to protect themselves from direct solar radiation and heat in exposed aeries. Parents, therefore, spend long periods of time shading the chicks to prevent them from overheating (18, 344). The paler plumage of chicks is considered a mechanism for thermoregulation in response to high sunlight exposure; the Eurasian Griffon is one of the few endotherm species in which this type of acclimating mechanism has been described (18).
Drinking, Pellet-Casting, and Defecation
The Eurasian Griffon gathers at temporary pools to drink (17). In the Eastern Rhodopes (Bulgaria and Greece), it used fountains and natural springs for drinking water throughout the year, more often during spring and summer (274).