Ontologia
Civette des Célebes

Civette des Célebes

Macrogalidia musschenbroekii(Schlegel, 1877)

VULR Monde (IUCN)
1 photo · Licences CC (Wikimedia Commons / iNaturalist)Click pour agrandir

Description

espèce de mammifères

Source : Wikidata

Pays · région · aire protégée · écorégion · biome

Graphe en cours d’indexation

Calcul du tissu écologique de Macrogalidia musschenbroekii.

Le graphe apparaîtra automatiquement dès que le calcul est terminé (rafraîchissement toutes les 5s).

Liste rouge IUCN

VU · Vulnérablecritères A2cd+3cd+4cd; C1Décroissante
Évaluation complète
Évaluation
2015 · v3.1
Altitude
02600 m
Profondeur
m
État de la populationExpert
The overall population status of Sulawesi Civet is very poorly known. Published records are very scarce (Wemmer et al. 1983, Wemmer and Watling 1986, Lee et al. 2003) and only 28 museum specimens are known (Veron 2001). Unpublished records and reports include: (1) Bakiriang Wildlife Sanctuary, central Sulawesi: a single individual observed by night in 2013; (2) an unconfirmed record from Bantimurung-Bulusaraung National Park in 1993; (3) Feruhumpenai-Matano Nature Reserve; and (4) Karaeng-Lompobattang Protection Forest (P. Wood pers. comm. 2014, Jihad pers. comm. 2014). There are also unconfirmed reports (rare sightings by local people) from a forest near Tomohon, 25 km south of Manado (J. Tasirin pers. comm. 2014) and from the Togian archipelago and Buton island (see the Geographic Range section).

Sulawesi Civet is evidently rare in, or locally absent from, some areas within its general geographic range. In the well-studied Tangkoko Reserve, it was not found in the only camera-trap survey to date, of about 1,000 camera-trap-nights over 0–1,000 m a.s.l. (J. Brodie pers. comm. 2015). In many years of intensive wildlife watching, Jukber Lambaihang (pers. comm. 2015) has never seen Sulawesi Civet at this site, although he has observed it in Lore Lindu National Park. Similarly, R. Hutchinson (pers. comm. 2015) has seen it only in Lore Lindu NP. In five full nights of spotlighting on foot on Sulawesi, V. Dinets (pers. comm. 2015) never found the species, and in 3–5 hours of night driving through forest, he had only one record: near Bogani Nani Wartabone National Park, 1–2 km from the park office. In south-east Sulawesi, Lee et al. (2003) found it in three of the five survey areas in which they camera-trapped, suggesting that it could be relatively widespread there, although they had only one record at each. Their encounter rate has been considered to suggest that the species is scarce in this part of the island, but it is difficult to make any deduction about abundance from this information. Lee et al. (2003) reported that they set their camera-traps 1–1.5 m above the ground: this is so much higher than is ideal for surveying small carnivores that it is likely to have depressed encounter rates, and in the same programme, they photographed Malay Civet only once, and Common Palm Civet not at all (I. Hunowu verbally 2008). The low total number of Sulawesi Civet photographs might simply reflect the low total effort. This was given as 23,485 hours (= 9,653 + 5,187 + 8,645, in three areas), which equates to 979 camera-trap-nights. Comparison with figures for palm civet camera-trapping in a range of sites across Myanmar (Than Zaw et al. 2008), where camera-traps were set 40–50 cm above ground, and thus more photographs of civets would be expected, gives no support that the results in Lee et al. of ‘only’ three photograph events indicate rarity of Sulawesi Civet. In roughly 27,700 trap-nights in Myanmar, there were 36 photograph events of Common Palm Civet Paradoxurus hermaphoditus, ten of Masked Palm Civet Paguma larvata and none of Small-toothed Palm Civet Arctogalidia trivirgata (which is almost wholly arboreal). For easier comparison, Lee et al. (2003) found Sulawesi Civet at 3.0 events per 1,000 trap-nights, exceeding Myanmar’s figures of 1.3 Common Palm Civet events per 1,000 trap-nights, 0.36 Masked Palm Civet events per 1,000 trap-nights, and 1.6 palm civet events (all species combined) per 1,000 trap-nights. If Sulawesi Civet is more active on the ground than are these palm civets, then a more relevant comparison with Myanmar would be with the ground-dwelling Large Indian Civet Viverra zibetha; Than Zaw et al. (2008) recorded this at 4.6 events per 1,000 trap-nights, only at 150% the rate at which Sulawesi Civet was being camera-trapped by Lee et al. (2003). This difference could simply reflect that in the heights at which the two survey programmes set their camera-traps. But in fact all evidence (notably Wemmer and Watling 1986) suggests that Sulawesi Civet is significantly arboreal, meaning that ground-level camera-traps (at least, non-baited ones) might well be less effective at detecting it than at finding Viverra civets. Moreover, the exact microhabitats at which camera-traps are set can have huge, though rarely quantified, effects on the frequency with which individual species are photographed. With only three events, the Lee et al. (2003) records do not allow any strong statement of the species’s abundance in this area. The considered opinion of Wemmer and Watling (1986: 8), based upon more field contact with the species than any other Western biologists, was that “in the Lore Lindu Reserve Macrogalidia was common”. Extrapolating this single-site conclusion to the whole island would be rash, but it underlines that there is as yet no real evidence that the species is genuinely rare in the areas where it occurs; nor indeed is there any that it is not rare. The paucity of records in trade or villages (see 'Theats') suggests that the species might be rare; although its part-aboreality might insulate it somewhat from the largely ground-operating traps used in most hunting on the island for animals of this size-class and above, it evidently spends significant time on the ground as shown by the finding of footprints by Wemmer and Watling (1986) and, perhaps, the camera-trapping of Lee et al. (2003), although it is not stated in the latter whether lures, which can bring arboreal animals to the ground, were used. Activity on the ground exposes it to various forms of trapping (see 'Threats'), and although in theory possible, it is implausible that bycatch Sulawesi Civets were abandoned in the field, it is more likely that few are caught.

There is no direct information on the population trend, but assuming that this species is indeed strongly reliant upon old-growth forest (see Wemmer and Watling (1986)), forest change can be used to suggest what might be the broad trend. According to Abood et al. (2014), Sulawesi lost about 20,000 km² of forest between 2000 and 2010, mostly in areas outside industrial concessions for timber, pulp and paper, oil palm and mining, According to the Ministry of Forestry (2011), Sulawesi had 101,172 km² of forest in 2010, of which 39,151 km² was primary, 61,854 km² secondary, and 167 km² planted forest. A total of 20,000 km² of forest loss between 2000 and 2010 would indicate that there was about 120,000 km² of forest in 2000, and that Sulawesi had lost 17% of its forest in this 10-year period. Assuming that these rates remained similar over a 15-year window (i.e., the last three generations, with one generation taken as five years; Pacifici et al. 2013), this indicates a decline in habitat of about 26%. Any losses within remaining habitat will be additional to this; given the level of conflict with livestock around Lore Lindu documented by Wemmer and Watling (1986) and increased fragmentation of Sulawesi’s forests since then, these losses are likely to be driving additional declines (see the Threats section).

Menaces identifiées(13 menaces classées CMP-IUCN)

  • 1_1
    Housing & urban areas
    Negligible declinesMinority (<50%)Ongoing
  • 1_2
    Commercial & industrial areas
    Negligible declinesMinority (<50%)Ongoing
  • 2_1_1
    Shifting agriculture
    Negligible declinesMinority (<50%)Ongoing
  • 4_1
    Roads & railroads
    Negligible declinesMinority (<50%)Ongoing
  • 5_1_1
    Intentional use (species is the target)
    Negligible declinesMajority (50-90%)Ongoing
  • 5_2_2
    Unintentional effects (species is not the target)
    Negligible declinesMajority (50-90%)Ongoing
  • 5_3_3
    Unintentional effects: (subsistence/small scale) [harvest]
    Negligible declinesMajority (50-90%)Ongoing
  • 5_3_4
    Unintentional effects: (large scale) [harvest]
    Negligible declinesMinority (<50%)Ongoing
  • 2_1_2
    Small-holder farming
    Slow, Significant DeclinesMajority (50-90%)Ongoing
  • 2_1_3
    Agro-industry farming
    Slow, Significant DeclinesMinority (<50%)Ongoing

+ 3 menaces supplémentaires

Description complète des menacesExpert
Sulawesi Civet can safely be stated to be threatened by forest loss, degradation and fragmentation, and perhaps by lethal control as a predator of livestock. Hunting and the effects of introduced carnivores are less likely to be driving population declines. The species was considered forest-dependent by Wemmer and Watling (1986), and no subsequent information contradicts this. Ongoing fragmentation of forest can be assumed to expose an ever-higher proportion of the population to retaliatory killing; it is a documented predator of livestock, with three of six conflicts investigated by Wemmer and Watling (1986) resulting in lethal control of the Sulawesi Civet in question.

In North Sulawesi, the impact of hunting on this species is probably low. No information was traced for other parts of the island, and given that ethnic groups may differ in their consumption patterns, the situation in North Sulawesi should not be assumed to hold for the rest of the island. Wemmer and Watling (1986) found no evidence around Lore Lindu that Sulawesi Civet is specifically sought for food, and plenty of circumstantial evidence that it is not. Various more recent market trade and village consumption surveys in North Sulawesi corroborate this. In 2011 surveys of wildlife meat in north Sulawesi markets by Selamatkan Yaki, a programme through Whitley Wildlife Conservation Trust (UK), did not find the species (T.A.C. Loffeld pers. comm. 2015). Two years of extensive trade surveys in North Sulawesi province in 2001–2003 detected nearly 7,000 wild mammals in road blockades of which fewer than 100 were (in total) small bats (Chiroptera), babirusas Babyrousa, macaques Macaca, cuscuses Phalanger and Stigocuscus, and civets, and almost 100,000 wild mammals in markets, of which only 1.2% were (in total) cuscuses, squirrels (Sciuridae), babirusas, macaques, tarsiers Tarsius, civets, anoas Bubalus, and deer Rusa timorensis (Lee et al. 2005). Similar surveys continued, and up to 2006 there seems to have been no record of Sulawesi Civet in any year (Wildlife Conservation Society per M. Leggett pers. comm. 2015). However, in 2007 one Sulawesi Civet was reported in a truck-load of wildlife meat inspected in Maelang, North Sulawesi province; the consignment was confiscated and buried (J. Tasarin pers.comm. 2015). In 2003, S. Siwu (pers. comm. 2015) photographed parts (including head and paws) of a Sulawesi Civet in Maeleng market. Based on almost continuous market surveys in Tomohon and Langowan from 2000 to 2014, L. Clayton (pers. comm. 2015) considers it to be, at most, rarely traded.

The Minahasans do not usually seek the species for consumption; their order of preferred wildlife meat is, in general, Sulawesi Wild Pig (Sus celebensis), fruit bats (Megachiroptera), white tailed forest rats (Rattus spp.), Reticulated Python (Python reticulatus), macaques, Water Monitor (Varanusalvator), cuscuses, and anoas. Less preferred species such as babirusas, civets, Maleo (Macrocephalon maleo) (meat) or tarsiers, if they are trapped or shot by hunters, may be sent opportunistically to market (J. Tasarin pers. comm. 2015). This is corroborated by intensive surveys of village consumption by the Selamatkan Yaki programme in 2011–2015. These found only four respondents stating that they had eaten or kept ‘musang’ (which could also refer to Malay Civet (Viverra tangalunga), or, if present, Common Palm Civet (Paradoxurus hermaphroditus)) as a pet. Although if another name were used for Sulawesi Civet, records of consumption would not have been picked up, this suggests a low incidence of in-village consumption in the surveyed areas. In 2011–2012, villages were spread through North Sulawesi: Agotey (Pineleng), Kumu (Tombariri), Wawona (Tatapaan), Paslaten (Tomohon Timur), Tinoor (Tomohon Utara), Rurukan (Tomohon Timur), Pangolombian (Tomohon Selatan), Molas (Bunaken), Kawatak (Langowan Selatan), Kasawari (Aertembaga), Airmadidi (Airmadidi), Pinilih (Dimembe), Dua Sudara (Ranowulu), Kombot (Pinolosian), Lolak (Lolak), Tudo Aog (Boloang), Liberia (Modayag), Sinsingon (Passi Timur) and Tondey (Motoling Barat); in each village 40 respondents were interviewed, resulting in 760 respondents. In 2013, there were 781 respondents in Tomohon and Langowan, in 2014, 1,135 in Airmadidi and Bitung, and in 2015, 764 in Tomohon and Langowan. No respondents mentioned that the eating of any animal was culturally avoided (T.A.C. Loffeld, H. Hilser and V. Melfi pers. comm. 2015). In these areas, most hunting is believed to be with ground snares, nets and dogs (J. Tasarin pers. comm. 2015, L. Clayton pers. comm. 2015, T.A.C. Loffeld pers. comm. 2015). Sulawesi Civet is believed to be largely arboreal (Wemmer and Watling 1986) and thus is might be at low risk from these methods. There is considerable arboreal snaring for rats, but the nooses are too small to catch Sulawesi Civet except by a limb; air-gun hunting perhaps would result in most animals taken (J. Tasarin pers. comm 2015).

Live wildlife markets on Java and Bali trade many civets, including those from Indonesian islands other than Java; no Sulawesi Civet has been noted in these surveys (Shepherd 2012, Nijman et al. 2014, V. Nijman pers. comm. 2015), nor have any come to the Cikananga rescue centre in Java, which has received other Sulawesi species (W. Eggen pers. comm. 2015). There are some ‘civet-lover clubs’ on Sulawesi but whether a significant number of members keep captive Sulawesi Civet has not been established; their internet content does, however, include advice on how to keep it (V. Nijman pers. comm. 2015). If civet-keeping were to rise dramatically in popularity there (as it has on Java; Nijman et al. 2014), and this species were to become a sought-after holding, then given the assumed low population of this species, targeted off-take might substantially exacerbate the rate of decline.

Non-native species of civet (Malay Civet and Common Palm Civet) and domestic cats and dogs might threaten Sulawesi Civet. However, given that it apparently is quite arboreal, none is likely to be a significant predator and the only likely strong competitor might be Common Palm Civet; but this species is scarce (probably not in fact naturalised) on Sulawesi (Wemmer and Watling 1986, Veron 2001). Moreover, on Buton island dogs and cats live in the forest only near villages and roads (Seymour et al. 2010); assuming this is true also for the mainland, they perhaps have little contact with Sulawesi Civet.

Habitats préférentiels (classification IUCN)

  • 1_6Forest - Subtropical/Tropical Moist Lowland
  • 1_9Forest - Subtropical/Tropical Moist Montane
  • 14_1Artificial/Terrestrial - Arable Land
  • 3_6Shrubland - Subtropical/Tropical Moist
  • 4_5Grassland - Subtropical/Tropical Dry
Mesures de conservation recommandéesExpert
Sulawesi Civet is known from several protected areas including Rawa Aopa National Park, Tanjung Peropa Wildlife Reserve, Mangolo Recreation Forest, Lore Lindu National Park (NP), and Bogani Nani Wartabone NP (Wemmer and Watling 1986, Lee et al. 2003, V. Dinets pers. comm. 2015). This species is totally protected in Indonesia (Shepherd 2008).

Understanding of the conservation status of many Asian small carnivores has advanced greatly since the mid 1990s with the widespread use of camera-trapping. This camera-trapping has, however, rarely been targeted at small carnivores: it often focuses on big cats Panthera and Neofelis, Asian Elephant (Elephas maximus), and other high-profile species. None of these inhabit Sulawesi; consequently, camera-trapping has been rather limited on the island, and Sulawesi Civet remains very poorly known. Nonetheless, various large mammals of high conservation concern on Sulawesi (babirusas Babyrousa, endemic macaques Macaca, and anoas Bubalus) receive some level of conservation research and intervention; camera-trapping and activities concerning these genera should be encouraged to seek and collate records of the endemic civet to allow a more informed assessment of its conservation needs.

Maintaining the habitat integrity of the forest protected area network of Sulawesi is probably the most important conservation intervention for this species. More precise recommendations for intervention require further investigation before formulation. More information is specifically needed about: (i) the extent to which retributory killing is a threat to the population rather than simply a cause of death for individuals; (ii) assessment whether the indications from North Sulawesi that there is no significant demand for trade or consumption apply across the island; (iii) evaluation of the relative merits of potential techniques to survey the species' distribution and population status, including, at least, baited and non-baited camera-trapping; (iv) use of the most effective and efficient detection method(s), to determine current distribution, population status and habitat use, specifically, how patchy within old-growth forest the occurrence is; (v) the extent to which the species is kept and desired by civet-lover clubs in Sulawesi and elsewhere in Indonesia. Clarification of any aspect of its natural history might also provide information of high management value.
Actions de conservation (6)Expert
  • 2_1Site/area management
  • 3_1_1Harvest management
  • 4_2Training
  • 4_3Awareness & communications
  • 5_4_2National level
  • 5_4_3Sub-national level
Stress écologiques (3)Expert
  • 1_1Ecosystem conversion
  • 1_2Ecosystem degradation
  • 2_1Species mortality
Priorités de recherche (7)Expert
  • 1_2Population size, distribution & trends
  • 1_3Life history & ecology
  • 1_4Harvest, use & livelihoods
  • 1_5Threats
  • 1_6Actions
  • 3_1Population trends
  • 3_4Habitat trends
Niche IUCN globaleExpert

Royaumes biogéographiques

Indomalayan

Systèmes (terrestre/eau douce/marin)

Terrestrial
Références bibliographiques (18)Expert
  1. IUCN. 2015. The IUCN Red List of Threatened Species. Version 2015-4. Available at: <a href="www.iucnredlist.org">www.iucnredlist.org</a>. (Accessed: 19 November 2015).
  2. Abood, S.A., Lee, J.S.H., Burivalova, Z., Garcia-Ulloa, J. and Koh, L.P. 2015. Relative contributions of the logging, fiber, oil palm, and mining industries to forest loss in Indonesia. <i>Conservation Letters</i> 8: 58–67.
  3. Nijman, V., Spaan, D., Rode-Margono, E.J., Roberts, P.D., Wirdateti and Nekaris, K.A.I. 2014. Trade in Common Palm Civet <i>Paradoxurus hermaphroditus</i> in Javan and Balinese markets, Indonesia. <i>Small Carnivore Conservation</i> 51: 11–17.
  4. Pacifici, M., Santini, L., Di Marco, M., Baisero, D., Francucci, L., Grottolo Marasini, G., Visconti, P. and Rondinini, C. 2013. Generation length for mammals. <i>Nature Conservation</i> 5: 87–94.
  5. Shepherd, C.R. 2012. Observations of small carnivores in Jakarta wildlife markets, Indonesia, with notes on trade in Javan Ferret Badger <i>Melogale orientalis</i> and on the increasing demand for Common Palm Civet <i>Paradoxurus hermaphroditus</i> for civet coffee production. <i>Small Carnivore Conservation</i> 47: 38–41.
  6. Brugiere, D. 2012. Sulawesi, Java and a bit of Sumatra. Unpublished report. Available at: <a href="http://223.27.200.5/mammalwatching.com/Oriental/Otherreports/DB%20Indonesia%202012.pdf">http://223.27.200.5/mammalwatching.com/Oriental/Otherreports/DB%20Indonesia%202012.pdf</a>. (Accessed: 15 April 2015).
  7. Ministry of Forestry. 2011. <i>Forestry statistics of Indonesia 2011</i>. Direktorat Jenderal Planologi Kehutanan, Kementerian Kehutanan, Jakarta, Indonesia.
  8. Seymour, A.S., Tarrant, M., Cox, R., Sharpe, A. and Woollam, T. 2010. Ecology of the top mammalian predator in the forests of Sulawesi, Indonesia. Unpublished report for Operation Wallacea.
  9. Shepherd, C.R. 2008. Civets in trade in Medan, North Sumatra, Indonesia (1997–2001) with notes on legal protection. <i>Small Carnivore Conservation</i> 38: 34–36.
  10. Than Zaw, Saw Htun, Saw Htoo Tha Po, Myint Maung, Lynam, A.J., Kyaw Thinn Latt and Duckworth, J.W. 2008. Status and distribution of small carnivores in Myanmar. <i>Small Carnivore Conservation</i> 38: 2–28.
  11. Lee, R.J., Gorog, A.J., Dwiyahreni, A., Siwu, S., Riley, J., Alexander, H., Paoli, G.D. and Ramono, W. 2005. Wildlife trade and implications for law enforcement in Indonesia: a case study from North Sulawesi. <i>Biological Conservation</i> 123: 477–488.
  12. Lee, R. J., Riley, J., Hunowu, I. and Maneasa, E. 2003. The Sulawesi Palm Civet: expanded distribution of a little known endemic viverrid. <i>Oryx</i> 37: 378-381.
  13. Veron, G. 2001. The palm civets of Sulawesi. <i>Small Carnivore Conservation</i> 24: 13–14.
  14. Schreiber, A., Wirth, R., Riffel, M. and Van Rompaey, H. 1989. <i>Weasels, civets, mongooses, and their relatives. An Action Plan for the conservation of mustelids and viverrids</i>. IUCN, Gland, Switzerland.
  15. Musser, G.G. and Dagosto, M. 1987. The identity of <i>Tarsius pumilus</i>, a pygmy species endemic to the montane mossy forests of central Sulawesi. <i>American Museum Novitates</i> 2867: 1–53.
  16. Wemmer, C. and Watling, D. 1986. Ecology and status of the Sulawesi Palm Civet. <i>Biological Conservation</i> 35: 1-17.
  17. Wemmer, C. 1983. External characters of the Sulawesi palm civet. <i>Journal of Mammalogy</i> 64(1): 133-136.
  18. Hooijer, D.A. 1950. Man and other mammals from Toalian sites in Southwestern Celebes. <i>Verh. kn. Ned. Akad. Wet. Natuurk</i> 46: 1–162.
Évaluateurs & contributeurs (3)Expert
assessor
Tasirin, J., Dinets, V., Meijaard, E., Brodie, J., Nijman, V., Loffeld, T.A.C., Hilser, H., Shepherd, C., Seymour, A.S. & Duckworth, J.W.
contributor
Hutchinson, R., Engelhardt, A., MacKinnon, J.R., Jihad, Clayton, L., Lambaihang, J., Wood, P., Purser, S., Hunowu, I., Hall, J., Eggen, W., Martin, T., Priston, N., Siwu, S. & Leggett, M.
evaluator
Hoffmann, M.

Tasirin, J., Dinets, V., Meijaard, E., Brodie, J., Nijman, V., Loffeld, T.A.C., Hilser, H., Shepherd, C., Seymour, A.S. & Duckworth, J.W. 2015. Macrogalidia musschenbroekii. The IUCN Red List of Threatened Species 2015: e.T12592A45198901. Accessed on 05 May 2026.

Traits biologiques

20 valeurs · 4 sources

Morphologie(4)

Masse adulte
5,15 kg
PanTHERIA
Longueur
-999 mm
PanTHERIA
Masse naissance
-999000 mg
PanTHERIA
Masse au sevrage
-999000 mg
PanTHERIA

Cycle de vie(1)

Longévité max
-999 mois
PanTHERIA
Voir 15 traits de plus (2 catégories)

Reproduction(6)

Gestation
-999 j
PanTHERIA
Intervalle naissances
-999 j
PanTHERIA
Taille de portée
-999
PanTHERIA
Portées par an
-999
PanTHERIA
Maturité sexuelle
-999 j
PanTHERIA
Sevrage
-999 j
PanTHERIA

Écologie & habitat(9)

Fruits (%)
40 %
elton_mammals
Invertébrés (%)
0 %
elton_mammals
Nectar (%)
0 %
elton_mammals
Autre végétal (%)
0 %
elton_mammals
Charognard (%)
0 %
elton_mammals
Graines (%)
0 %
elton_mammals
Vert. ectothermes (%)
0 %
elton_mammals
Vert. endothermes (%)
60 %
elton_mammals
Poissons (%)
0 %
elton_mammals

Sources priorisées par qualité scientifique (peer-reviewed spécialisées → Wikidata fallback). Unités auto-converties, valeur max retenue en cas de mesures multiples. Méthodologie · Citations.

Répartition mondiale (heatmap GBIF)Construction en cours

0 obs · 0 cellules
Construction par partitions temporelles GBIF0%

Source : GBIF — observations agrégées par hexagones 0.2° × 0.2° (~22km). Filtre qualité : précision coordonnée < 10 km. Coloration quantile (q50/70/90/99). Fond carte : OpenFreeMap · © OpenStreetMap.

Distribution mondiale

Calcul de la distribution GBIF· ~10–60 s

Phénologie

Calcul du calendrier d'apparition· ~5–30 s

Consulter sur les bases externes

Observations & statuts

Cartographie

Bibliographie

Note nomenclaturale & synonymesExpert

Note nomenclaturale

TAXREF v18 — INPN/MNHN

Synonymes (1)— redirigent vers cette page

  • Paradoxurus musschenbroekiiSchlegel, 1877

Sources : Catalogue of Life Cross-References (synonymes) · TAXREF v18 INPN/MNHN (commentaires FR).