Notice bibliographique
Résumé
59. Pallas’s Squirrel Callosciurus erythraeus French: Ecureuil de Pallas / German: Pallas-Schénhérnchen / Spanish: Ardilla de Pallas Other common names: Formosan Squirrel, Red-bellied Squirrel Taxonomy. Sciurus erythraeus Pallas, 1779, Original type locality not known. Restrict- ed by J. L. Bonhote in 1901 to Assam, In- dia, and further restricted by J. C. Moore and G. H. H. Tate in 1965 to the Garo Hills of Assam. Reports of this squirrel often occur under the name C. flavimanus. Significant further study of the many named and the likely many as yet undocumented subspecies is required; it is possible that some may merit species level distinction. Generally, 26 subspecies are recognized, some of which were divided into four groups as below by G. B. Corbet and J. E. Hill, 1992. Subspecies and Distribution. The C. e. erythraeus group, Sikkim to Assam, India to Myanmar, W Thailand and Peninsular Malaysia, N Vietnam, and Taiwan: C.e.gordoniJ.Anderson,1871—NMyanmar. C.e.shanicusRyley,1914—NCMyanmar. C.e.bhutanensisBonhote,1901—Bhutan. C.e.rubeculusMiller,1903—Pahang,Malaya. C.e.erythraeusPallas,1779—GaroHillsofMeghalaya,India. C.e.erythrogasterBlyth,1842—Wbank,ChindwinRiver,Myanmar. C.e.castaneoventrisGray,1842—Hainan,China. C.e.atrodorsalisGray,1842—areasurroundingMawlamyaing,Myanmar. C.e.thaiwanensisBonhote,1901—NWTaiwan.TheC.e.flavimanusgroup,Laos,Cambodia,andSVietnam: C.e.flavimanus1.GeoffroySaint-Hilaire,1831—CVietnam.TheC.e.sladenigroup,betweentheChindwinandIrrawaddyriversofMyanmar: C.e.harringtoniThomas,1905—areasurroundingHomalin,upperChindwin,Myanmar. C.e.intermediusJ.Anderson,1879—Assam,India. C.e.sladeniJ.Anderson,1871—Thizyain,upperMyanmar.TheC.e.styanigroup,EChina: C.e.ningpoensisBonhote,1901—vicinityofNingbo,China. C.e.styaniThomas,1894—Kahing,SEChina.OthersubspeciesnotassignedtoagroupbyCorbetandHill: C.e.bartoniThomas,1914—upperChindwin,Myanmar. C.e.bonhoteiRobinson&Wroughton,1911—Chinchiensan,Sichuan,China. C.e.gloverThomas,1921—Nagchuka,WSichuan,China. C.e.grisesmanusMilne-Edwards,1867—nearSaigon,Vietnam. C.e.hendeeiOsgood,1932—NVietnam. C.e.hyperythrusBlyth,1856—SMyanmar,SWThailandonMalayPeninsula. C.e.michianusRobinson&Wroughton,1911—Yunnan,China. C.e.pranisKloss,1916—KohLok,Pran,SThailand. C.e.siamensisGray,1860—Thailand. C.e.thaiKloss,1917—Raheng,CThailand. C. e. zimmeensis Robinson & Wroughton, 1916 — Chiang Mai, N Thailand. This species is found in much of C & S China (including Hainan I), Taiwan, NE India, Bangladesh, and mainland South-east Asia. Introduced and naturalized in Japan (S Honshu, Kyushu, and several surrounding small islands), Hong Kong, Western Europe (the Netherlands, Belgium, and France), and Argentina. Descriptive notes. Head-body 209-227 mm, tail 176-216 mm; weight 286-375 g. There is considerable variation in the coloration among the forms of Pallas’s Squirrel. It is generally recognizable by the reddish coloration of venter (varying from dark maroon to creamy buff) and the olive-brown agouti dorsum. Nominate subspecies erythraeus group has reddish brown or reddish (sometimes agouti) underparts, commonly with a mid-ventral wedge or stripe of agouti dividing reddish brown coloration into two parts. Subspecies flavimanus group has feet that are paler than dorsum and (usually) venter. Subspecies sladeni group has a muzzle and feet that are similar in color to venter. Subspecies styani group has a venter that is pale cream to dull orange-brown; dorsum is pale and gray; and feet are agouti but not dark. Chromosome number is 2n = 40; FN = 70-72. Karyotype consists of seven pairs of metacentric autosomes, eight pairs of submetacentric autosomes, two pairs of subtelocentric autosomes, two pairs of telocentric autosomes, a metacentric X chromosome, and a subtelocentric Y chromosome. Chromosomal complement of subspecies flavimanus is 2n = 40; FN = 74. Habitat. Primary and secondary subtropical montane evergreen and broadleaved forests. In China, Pallas’s Squirrel is present in subalpine coniferous forests, or in a mix of conifer and broadleaf trees, at elevations above ¢.3000 m; occursalso in tropical and subtropical forests at lower elevations. In far northern Laos,it is found in heavily degraded scrub landscapes with small degraded forest patches. It will occupy pine (Pinus, Pinaceae) plantations that are more than 16 years old if protected, but, in unprotected areas, not until plantations are 31 years old, apparently because human activities decrease important vegetation diversity on forest floor. In Peninsular Malaysia, Pallas’s Squirrel is described as being common in forests and woodlands in the hills. It was introduced to Tomogashima Island in Japan, where it prefers both broadleaved and coniferous evergreen trees. In Argentina, these introduced squirrels are reported in fruit plantations. Food and Feeding. Overits wide distribution, Pallas’s Squirrel seems to be extremely adaptable in its diet. On Tomogashima Island, Japan,it feeds extensively on camellia flowers (Camellia japonica, Theaceae), bayberry fruits (Myrica rubra, Myricaceae), and Japanese pine seeds (Pinus thunbergii, Pinaceae). In total, it eats 36 species of plants there: mainly camellia blossoms in January-March, leaves in April and May, and fruits (mostly seeds) in June-December. In addition, it consumes the bark of 23 plant species, eats insects (mostly ants and cicadas), and drinks water that accumulates in knotholes. In China,it has also been reported to feed on bird eggs and fledglings. In Malaysia, the stomach contents of three individuals included a significant proportion of insects, as well as starchy vegetable matter. Breeding. Mating bouts start early in the morning and last for many hours. The most dominant male chases other males away and then breeds with the female, after which he guards the female for an average of 33 minutes by giving the post-copulatory call, causing nearby males and the female to adopt their immobile anti-predator response. The female subsequently mates with another male, mating 4-11 timesin all during her estrus. Although not specified in the study, the assumption is that these other males also give a post-copulatory call. Mating bouts occur throughout the year, and the average litter size at weaning is 1-4 individuals. Activity patterns. There is no specific information available for this species, but Pallas’s Squirrel is diurnal and arboreal. Movements, Home range and Social organization. In Kamakura City, Japan, where they have been introduced and are now common, both males and females have overlapping home ranges, with fewer females overlapping with other females (2-3 in winter—spring, 1-6 in autumn-winter) than males overlapping with other males (12-6 in winter—spring, 8-7 in autumn-winter). Male home ranges were 2:6 ha in the winter— spring season and 1-2 ha in the autumn-winter season. Female home ranges were 0-7 ha and 0-5 ha in the same two seasons. Status and Conservation. Classified as Least Concern on The IUCN Red List. Pallas’s Squirrel is widely distributed, has a presumed large population, and has a tolerance of some degree of habitat modification. There are no major threats to this species, although hunting for local consumption has depleted some South Asian populations. Bibliography. Bertolino (2009), Bonhote (1901), Duckworth, Timmins & Molur (2008), Corbet & Hill (1992), Guichon et al. (2005), Jordan et al. (2005b), Lurz et al. (2013), Men Xingyuan et al. (2006), Moore & Tate (1965), Oshida et al. (2006), Setoguchi (1990, 1991), Shankar Raman et al. (1995), Smith & Yan Xie (2008), Tamura (1995), Tamura et al. (1988), Thorington et al. (2012).
Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.
Comment cette classification a été obtenuedéplier
Prédiction machine sur la base complète
Imitation des enseignantsNi prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.
Scores du classifieur distillé par catégorie (deux têtes)
| Catégorie | Codex | Gemma |
|---|---|---|
| Métarecherche | 0,000 | 0,000 |
| Méta-épidémiologie (sens strict) | 0,000 | 0,000 |
| Méta-épidémiologie (sens large) | 0,000 | 0,000 |
| Bibliométrie | 0,002 | 0,001 |
| Études des sciences et des technologies | 0,001 | 0,000 |
| Communication savante | 0,000 | 0,000 |
| Science ouverte | 0,000 | 0,001 |
| Intégrité de la recherche | 0,000 | 0,000 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,007 | 0,004 |
Scores machine (provisoires)
Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.
Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.
score_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découleClassification
machine, non validéePrédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.
Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».