Cryptoprocte féroce
Cryptoprocta feroxBennett, 1833
Graphe en cours d’indexation
Calcul du tissu écologique de Cryptoprocta ferox.
Le graphe apparaîtra automatiquement dès que le calcul est terminé (rafraîchissement toutes les 5s).
Liste rouge IUCN
VU · Vulnérablecritères A2cde+3cde+4cde↘Décroissante- Évaluation
- 2016 · v3.1
- Altitude
- 0 – 2600 m
- Profondeur
- – m
État de la populationTexte officiel évaluation IUCNExpert
Densities for the eastern forests are hypothesised by some to be at one-third those of the west, based on photo-trapping and cage trapping efforts throughout the humid forests (L. Dollar pers. comm. 2007). Subjective encounter rate is much higher in the western forests (particularly in Menabe, Bemaraha and Ankarana reserves) than in rainforests (F. Hawkins pers. comm.), but densities could well be similar between dry and humid forests. This is an important point for future investigation. Important determinants of density may include densities of lemur prey species, and levels of hunting.
Gerber et al. (2012) estimated the total Fosa population at between 2,635 (the population estimated to occur in protected areas) and 8,626 adults. Of the upper estimate, 4,476 are estimated to be in 32 populations in rainforest, and 4,150 in 38 populations in dry forest. In their estimation, 95% of the rainforest population occurred in forest blocks north of Andasibe-Perinet; the only protected areas in this region capable of holding more than 300 adult Fosas are Vohidrazana-Zahamena and Makira-Masoala. Around 95% of the dry forest population was in nine large forest blocks, of which only two could hold more than 300 individuals.
Gerber et al. (2012) found Fosa densities around Ranomafana National Park to be similar in primary forest (0.12 ± SE 0.05 individuals/km2) and logged forest (0.09 ± SE 0.04), and found the species in forest fragments 2.5 km from intact forest, although not in fragments 15 km from intact forest.
In northeast Madagascar, camera trap surveys by Farris (et al. in review a, pers. comm. 2014) found a high probability of occupancy (defined as the probability that a site/forest is occupied by the species of interest while taking into account the variation in detectability of the species across the various sites) of 0.68 ± SE 0.08 for Fosa across the Masoala-Makira landscape. Fosas had similar probabilities of occupancy in non-degraded forest (0.66 SE ± 0.06) and degraded forest (0.68 SE ± 0.13). Surveys at one contiguous forest site showed little to no change in Fosa occupancy (0.79 to 0.85) between 2008 and 2013 (trap success [number of captures divided by trap nights multiplied by 100] changed from 3.04 in 2008 to 3.42 in 2013). However, at another survey site, trap success decreased from 7.16 (2011) to 3.43 (2013) over a three-year period (Z. Farris pers. comm. 2014). Fosa occurred in forest fragments at Farankarina managed area, separated by at least 5 km from both Makira and Masoala National Parks, as well as in additional smaller fragmented forest patches. The smallest fragmented forest patch Fosa was recorded in was the 8 km2 Farankarina managed area (-15.422, 49.837), which lies at least 5 km from both Masola and Makira forests. Fosa was also observed moving through anthropogenic landscapes.
Menaces identifiées(9 menaces classées CMP-IUCN)
5_1_1Intentional use (species is the target)Rapid DeclinesMajority (50-90%)Ongoing5_1_3Persecution/controlRapid DeclinesMajority (50-90%)Ongoing8_1_1Unspecified speciesRapid DeclinesWhole (>90%)Ongoing8_1_2Named speciesRapid DeclinesWhole (>90%)Ongoing8_1_2Named speciesRapid DeclinesWhole (>90%)Ongoing8_1_2Named speciesRapid DeclinesWhole (>90%)Ongoing5_3_5Motivation Unknown/UnrecordedCausing/Could cause fluctuationsMajority (50-90%)Ongoing7_1_3Trend Unknown/UnrecordedCausing/Could cause fluctuationsMinority (<50%)Ongoing2_1_1Shifting agricultureSlow, Significant DeclinesWhole (>90%)Ongoing
Description complète des menacesTexte détaillé évaluation IUCNExpert
Household surveys (Farris et al. in review a) found 99 Fosas reportedly consumed within four villages (144 households were surveyed) from 2005 to 2011 across the Makira Natural Park. Hunting rates were highest in non-degraded forest and were positively associated with Fosa occupancy, meaning that hunters appear to be focusing their efforts in non-degraded forest where Fosa is most abundant. Golden et al (in press) report four Fosas hunted in one year at Betampona Strict Nature Reverve, two hunted opportunistically (presumably with dogs). Household interviews conducted by Madagasikara Voakajy (pers. comm. 2014) in the Moramanga region of eastern Madagascar between 2008 and 2009 suggest that 325 (21%) of 1,535 respondents interviewed in 129 villages had eaten Fosa in the preceding year.
Hunting is presumed to have increased significantly in many parts of the species' range since 2009 because of less effective governance and increased social instability following a coup d'etat.
Deforestation and forest disturbance across the range of the Fosa has increased significantly since 2009. R. Rajaonson (pers. comm. 2014) estimates that deforestation in eastern forest increased from 0.5% per annum in 2005-2010 to 0.94% per annum in 2010-2013. Allnut et al. (2009) estimated that in Masoala National Park, annual rates of deforestation in the studied area increased to 1.27% per annum in 2011. High levels of illegal settlement in protected areas, especially around the Bay of d'Antongil, are linked to artisanal mining (for quartz) and logging of rosewood; hunting for food using dogs has increased greatly in these areas as a result. Some villages have seen increases in populations of between 200 and 300% (C. Golden pers. comm. 2014). Around Ranomafana National Park, Fosa is absent from forest fragments more than 15 km from core habitat and is about equally often detected in degraded and primary habitats (Gerber et al. 2012)
In western Madagascar, Zinner et al. (2014) showed that for central Menabe, one of the most important centres of Fosa distribution, deforestation rates of 0.78 km2/yr in 2003-2006 increased to 1.09 km2/yr in 2006-2008, and to 2.55 km2/yr by 2008-2010. There is ample evidence that the increase continued in 2010-2014, coupled with increased illegal logging and hunting in the core forest areas, which will undoubtedly negatively effect populations of all native carnivores, especially through the increased presence of dogs.
The Fosa also preys on domestic fowl and is consequently killed as a pest by local people. It seems very susceptible to hunting, and is often targeted by groups engaged in collective group hunting (e.g. in the Makira forests) specifically for the purpose of eradication. Its parts are used for medicinal purposes. Competition with introduced carnivores occurs, including predation by feral dog packs. The Fosa seems to be more nocturnal when in the same areas as highly active diurnal people and dogs. High nocturnal activity overlaps with activity of both Small Indian Civet Viverricula indica and feral/wild cats, revealing the potential for increased interactions and competition (Farris et al. in review b).
Many camera-trap photographs of Fosas show animals carrying nooses from make-shift traps, and many show individuals with numerous scars and missing body parts (ears, lips, tails) which reportedly result from locals trying to kill them with machetes when they raid their livestock.
Habitats préférentiels (classification IUCN)
1_5Forest - Subtropical/Tropical Dry★1_6Forest - Subtropical/Tropical Moist Lowland★1_9Forest - Subtropical/Tropical Moist Montane★
Mesures de conservation recommandéesStratégies de conservation IUCNExpert
Actions de conservation (8)Conservation Actions Classification Scheme — IUCNExpert
2_1Site/area management3_1_1Harvest management4_3Awareness & communications5_1_2National level5_1_3Sub-national level5_2Policies and regulations5_4_2National level5_4_3Sub-national level
Stress écologiques (11)Stresses Classification — IUCNExpert
1_1Ecosystem conversion1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation2_1Species mortality2_1Species mortality2_1Species mortality2_3_2Competition2_3_2Competition2_3_2Competition2_3_2Competition
Usage & commerce (2)Use & Trade — IUCNExpert
1Food - humansubsistance3Medicine - human & veterinarysubsistance
Priorités de recherche (5)Research Needed Classification — IUCNExpert
1_4Harvest, use & livelihoods1_5Threats1_6Actions3_1Population trends3_2Harvest level trends
Niche IUCN globaleRealms · Systems · LMEs · Growth forms · FAOs — biogéographie IUCNExpert
Royaumes biogéographiques
Systèmes (terrestre/eau douce/marin)
Références bibliographiques (17)Sources scientifiques de l'évaluation IUCNExpert
- Farris, Z.J., Gerber, B., Kelly, M.J., Karpanty, S., Murphy, F. and Andrianjakarivelo, V. In review b. When the carnivores roam: temporal patterns and partitioning among Madagascar’s native and exotic carnivores.
- Farris, Z.J., Golden, C., Karpanty, S., Murphy, A., Stauffer, D., Andrianjakarivelo, V., Ratelolahy, F., Holmes, C. and Kelly, M.J. In review a. Effects of poaching, micro-habitat and landscape variables, human encroachment, and exotic species on Madagascar’s endemic and exotic carnivore community across the Masoala-Makira landscape.
- IUCN. 2016. The IUCN Red List of Threatened Species. Version 2016-1. Available at: <a href="www.iucnredlist.org">www.iucnredlist.org</a>. (Accessed: 30 June 2016).
- Golden, C.D., Rabehatonina, J.C.G., Rakotoarisoa, A. and Moore, M. 2014. Socio-ecological analysis of natural resource use near Betampona Strict Natural Reserve. Madagascar Conservation and Development. (in press).
- Zinner, D., Wygoda, C., Razafimanantsoa, L., Rasoloarison, R., Andrianandrasana, H.T. and Ganzhorn, J.U. 2014. Analysis of deforestation patterns in the Central Menabe, Madagascar, between 1973 and 2010. <i>Regional Environmental Change</i> 14: 157-166.
- Allnut, T.F., Asner, G.P., Golden, C.D. and Powell, G.V.N. 2013. Mapping recent deforestation and disturbance in northeastern Madagascar. <i>Tropical Conservation Science</i> 6: 1-15.
- Goodman, S. 2012. <i>Les Carnivora de Madagascar</i>. Association Vahatra, Antananarivo, Madagascar.
- Gerber, B.D., Karpanty, S.M. and Randrianantenaina, J. 2012. The impact of forest logging and fragmentation on carnivore species composition, density and occupancy in Madagascar's rainforests. <i>Oryx</i> 46: 414-422.
- Farris Z.J. and Kelly, M.J. 2011. A preliminary assessment of carnivores across the Makira Protected Area, Madagascar: results from a WCS pilot camera study. Wildlife Conservation Society, Antananarivo, Madagascar.
- Hawkins, C.E. and Racey, P.A. 2005. Low population density of a tropical forest carnivore, <i>Cryptoprocta ferox</i>: implications for protected area management. <i>Oryx</i> 39: 35-43.
- Hawkins, C.E. 2003. <i>Cryptoprocta ferox</i>, Fossa, Fosa. In: S.M. Goodman and J.P. Benstead (eds), <i>The Natural History of Madagascar</i>, pp. 1361-1363. The University of Chicago Press, Chicago, USA and London, UK.
- Garbutt, N. 1999. <i>Mammals of Madagascar</i>. Pica Press, East Sussex, UK.
- Bininda-Emonds, O.R.P., Gittleman, J.L. and Purvis, A. 1999. Building large trees by combining phylogenetic information: a complete phylogeny of the extant Carnivora (Mammalia). <i>Biological Reviews of the Cambridge Philosophical Society</i> 74: 143-175.
- Hornsey, T. 1999. Breeding the Fossa at Suffolk Wildlife Park. <i>International Zoo News</i> 46(7): 296.
- Hawkins, C.E. 1998. The behaviour and ecology of the Fossa, <i>Cryptoprocta ferox</i> (Carnivora: Viverridae) in a dry deciduous forest in western Madagascar. Ph.D. Thesis, University of Aberdeen.
- Goodman, S.M. 1996. The carnivores of the Reserve Naturelle Integrale d'Andringitra, Madagascar. <i>Fieldiana: Zoology</i>: 289-292.
- 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.
Évaluateurs & contributeurs (3)Personnes ayant contribué à l'évaluation IUCNExpert
Hawkins, F. 2016. Cryptoprocta ferox. The IUCN Red List of Threatened Species 2016: e.T5760A45197189. Accessed on 05 May 2026.
Traits biologiques
Morphologie(5)
Cycle de vie(1)
Voir 15 traits de plus (2 catégories)Replier
Reproduction(6)
Écologie & habitat(9)
Sources priorisées par qualité scientifique (peer-reviewed spécialisées → Wikidata fallback). Unités auto-converties, valeur max retenue en cas de mesures multiples. Méthodologie · Citations.