Ontologia
Phoque moine d'Hawaï

Phoque moine d'Hawaï

Neomonachus schauinslandi(Matschie, 1905)

VULR Monde (IUCN)
  1. Animal
  2. Chordata
  3. Mammalia
  4. Carnivora
  5. Phocidae
1 photo · Licences CC (Wikimedia Commons / iNaturalist)Click pour agrandir
Pays · région · aire protégée · écorégion · biome
Chargement du graphe…

Indicateurs du réseau écologique

Comment lire ce graphe

Ce graphe représente les interactions écologiques documentées entre Neomonachus schauinslandi et d'autres espèces, à partir de la base GloBI (Global Biotic Interactions, agrégation mondiale de la littérature scientifique) — source principale, complétée par d'autres jeux de données d'interactions agrégés par Ontologia. Il faut le comprendre comme une carte du savoir documenté, pas une carte de la réalité écologique exhaustive.

Limites principales

  • Incomplet. La majorité des interactions écologiques en milieu naturel n'ont jamais été publiées. Une espèce sans liens visibles n'est pas isolée — elle est probablement mal étudiée.
  • Biais publication pharmaco-agronomique. La littérature des interactions est polarisée par les enjeux économiques et sanitaires : parasitism / pathogen sur-pondéré sur les mammifères (recherche zoonoses, vecteurs), herbivory sur-pondéré sur les insectes phytophages (entomologie agronomique). À l'inverse, mutualisms, commensalisms et interactions sol/microbiote sont sous-cités. Conseil de lecture : sur les hubs mammifères ou les insectes ravageurs de culture, lire les arêtes parasitism / herbivory dominantes relativement au contexte de littérature, pas comme une mesure d'intensité écologique brute. Détails §10.1.
  • Biaisé vers les espèces étudiées. Quelques espèces (oiseaux communs, abeille mellifère, espèces modèles) concentrent disproportionnellement plus d'interactions documentées. Notre score composite ajoute un malus aux hubs de littérature pour atténuer cette dominance visuelle.
  • Interactions documentées globalement. Toutes les espèces affichées sont observées en France métropolitaine (les observations sont filtrées sur le territoire métropolitain), mais les interactions entre elles proviennent de la littérature scientifique mondiale. Une interaction documentée à l'étranger peut ne pas se réaliser à l'identique sur votre territoire. Le filtre « restreindre à ma commune » tient compte de la co-occurrence spatiale locale mais ne garantit pas l'interaction effective.
  • Sans dimension temporelle. Les variations saisonnières (migration, floraison, cycle de vie) ne sont pas modélisées.
  • Force d'interaction approximative. L'épaisseur des liens reflète le nombre de fois où l'interaction a été rapportée dans la littérature, pas son importance écologique réelle.

Comment nous sélectionnons les espèces affichées

Le graphe affiche au plus 31 nœuds par fiche (1 centre + 15 bulles depth=1 + 15 partenaires depth=2). Le serveur sélectionne intelligemment :

  • Bulles famille créées si une cascade taxonomique existe ou si ≥3 espèces directement documentées partagent une même famille — les espèces sont absorbées dans la bulle (pas de doublon visuel)
  • Espèces individuelles uniquement quand <3 dans une famille (sans cascade) — relations directes documentées
  • Pas d'espèces inférées affichées en doublon — les cascades sont représentées via les bulles famille uniquement
  • Partenaires depth=2 sélectionnés via algo priorité : candidat partagé par ≥2 docs de la famille (food web central) → reliant entre bulles → top sum_obs en dernier recours
  • Sous-types GloBI traduits en français au survol de la flèche (chasse, parasite, parasitoïde, mycorhize…)

Le toggle Profondeur 1 ↔ 2 client-side cache ou affiche les partenaires depth=2 sans refetch. Filtres règne, type d'interaction, ordres/familles, patrimoniales et commune recalculent côté serveur (slow path live ~1-2 s).

Indicateurs avancés (mode expert) : Modularité Q (Newman 2006, PNAS), communautés (Louvain, Blondel et al. 2008, J. Stat. Mech.), nestedness NODF (Almeida-Neto et al. 2008, Oikos).

Source : GloBI · TAXREF v18 (INPN/MNHN) · BDC-Statuts · Wikidata

32 partenaires écologiques documentés directement dans GloBI.

Partenaires
32
Espèces avec interactions documentées
Types d'interactions
7
Prédation, pollinisation, parasitisme…
Connectance
0.058
Densité des liens dans le sous-graphe affiché
Rang animalia
90 %
Percentile vs ensemble des animalia

Liste rouge IUCN

VU · Vulnérablecritères D1Croissante
Évaluation complète
Évaluation
2025 · v3.1
Altitude
3 m
Profondeur
550 m
État de la populationExpert
Hawaiian Monk Seals are distributed throughout the Hawaiian Islands. Within the Monk Seal’s range, two regions are often distinguished: the NWHI, comprising eight subpopulations located on remote atolls and small islands, and the MHI, comprising eight large high islands and associated small islets. Seals in the MHI are considered to be a single subpopulation. Published literature on Hawaiian Monk Seals typically refer to the aforementioned geographic aggregations as “subpopulations”, but they do not constitute subpopulations according to the IUCN Red List Guidelines definition. Hawaiian Monk Seals are non-migratory and tend to remain near where they were born. However, movement between areas is not uncommon (Johanos et al. 2014), allowing for gene flow throughout the range. Genetic analysis indicates the species is a single panmictic population (Schultz et al. 2011).

The status of the Hawaiian Monk Seal is assessed nearly every year and updated by the US National Marine Fisheries Service’s Pacific Islands Fisheries Science Center. The most recent reliable abundance estimates, from 2022, were used for this assessment.

The generation time for Hawaiian Monk Seals, estimated as the average age of reproducing individuals, is approximately 15 years. The best estimate of the total number of seals of all age classes in 2022 is 1,607. The population includes an estimated 922 sexually mature seals (NMFS unpublished data).

The earliest synoptic counts of Monk Seals throughout most of their range occurred in 1958 and consisted of index counts (total number of seals observed on shore), as opposed to an estimate of total population size (Kenyon and Rice 1959, Rice 1960). These counts included the six NWHI subpopulations from Kure Atoll to French Frigate Shoals (excluding Necker and Nihoa Islands). A negligible number of seals, if any, occurred in the MHI at that time. The sum of index counts at the same six NWHI subpopulations reached a low in 2013, at a level 70% below the estimate for 1958. A declining trend persisted for over five decades.

Prior to the 1990s, Monk Seals were rarely seen within the MHI, but the population has expanded since that time and by 2022 the MHI population accounted for approximately one-quarter of the species total abundance (Baker and Johanos 2004, Baker et al. 2011a, Carretta et al. in press).

The growth of the MHI subpopulation and generally improved juvenile survival in the NWHI together accounted for an estimated 2% (95% confidence interval 0.02–0.03) annual growth rate from 2013 to 2022.

Menaces identifiées(9 menaces classées CMP-IUCN)

  • 5_4_4
    Unintentional effects: (large scale) [harvest]
    Causing/Could cause fluctuationsMinority (<50%)Past, Unlikely to Return
  • 6_2
    War, civil unrest & military exercises
    Causing/Could cause fluctuationsMinority (<50%)Past, Unlikely to Return
  • 8_1_1
    Unspecified species
    Causing/Could cause fluctuationsMinority (<50%)Future
  • 9_2_3
    Type Unknown/Unrecorded
    Causing/Could cause fluctuationsMinority (<50%)Unknown
  • 5_4_5
    Persecution/control
    Negligible declinesMinority (<50%)Ongoing
  • 6_1
    Recreational activities
    Negligible declinesMinority (<50%)Ongoing
  • 6_3
    Work & other activities
    Negligible declinesMinority (<50%)Ongoing
  • 5_4_3
    Unintentional effects: (subsistence/small scale) [harvest]
    UnknownMinority (<50%)Ongoing
  • 11_1
    Habitat shifting & alteration
    Slow, Significant DeclinesWhole (>90%)Ongoing
Description complète des menacesExpert
Historical threats to Monk Seals were documented in (Ragen 1999) and (Ragen and Lavigne 1999). The most recent Recovery Plan (National Marine Fisheries Service 2007) updated the threats to the species and concluded that the most crucial threats in the NWHI at that time were: 1) food limitation that could be due to changes in oceanographic conditions, legacy impacts of fisheries, or competition with other predators; 2) entanglement in marine debris, largely fragments of net and line abandoned, lost, or discarded by North Pacific fisheries; 3) predation by sharks, especially on pre-weaned and recently weaned pups; and 4) intraspecific aggression by male seals. Loss of terrestrial habitat due to sea level rise resulting from global warming was first identified as an emerging threat in the NWHI by (Baker et al. 2006), but has recently become undeniably more concerning (Baker et al. 2020a). In the NWHI, most of the terrestrial habitat used by seals comprises low-lying sand islands. The historically most-used pupping habitat at French Frigate Shoals, has been almost entirely lost to inundation due to gradual erosion and destructive storm events (Baker et al. 2020a). This habitat loss has been associated with extraordinarily high mortality of young pups. Additional losses of terrestrial habitat due to sea-level rise will most likely reduce the carrying capacity of various NWHI populations or in some cases, may render significant portions of the species range inaccessible (Reynolds et al. 2012, Baker et al. 2020a).

Threats to Monk Seals in the MHI are quite distinct from those in the NWHI, and include: 1) intentional killing by humans, 2) fisheries interactions, primarily hookings and entanglements in gillnets; 3) transmission of diseases from terrestrial animals to the seals, with toxoplasmosis being a primary concern (Barbieri et al. 2016, Gobush et al. 2017, Harting et al. 2020, Robinson et al. 2023). In recent decades, as the monk seal population has grown in the MHI where seals are more exposed to anthropogenically-impacted landscapes and domestic animals, infection with Toxoplasma gondii (a parasite for which cats are the obligate hosts) has emerged as one of the primary health threats limiting recovery of Monk Seals (Barbieri et al. 2016, Harting et al. 2020, Robinson et al. 2023).

Habitats préférentiels (classification IUCN)

  • 10_1Marine Oceanic - Epipelagic (0-200m)
  • 10_2Marine Oceanic - Mesopelagic (200-1000m)
  • 12_1Marine Intertidal - Rocky Shoreline
  • 12_2Marine Intertidal - Sandy Shoreline and/or Beaches, Sand Bars, Spits, Etc
  • 13_1Marine Coastal/Supratidal - Sea Cliffs and Rocky Offshore Islands
  • 9_1Marine Neritic - Pelagic
Mesures de conservation recommandéesExpert
The Hawaiian Monk Seal has been listed as Endangered under the US Endangered Species Act since1976. That law contains a number of provisions to protect the seals and their critical habitat. They are also covered by a general prohibition of unpermitted taking by the US Marine Mammal Protection Act of 1973.

Virtually all of the land and waters in the NWHI is included in one or more protected areas (the Northwestern Hawaiian Islands State Marine Refuge, the Kure Atoll State Wildlife Refuge, the Hawaiian Islands National Wildlife Refuge, the Midway Atoll National Wildlife Refuge, the Northwestern Hawaiian Islands Coral Reef Ecosystem Reserve, and the Papahānaumokuākea Marine National Monument), where in situ human activities that could affect the seals or their habitats are either prohibited or strictly controlled.

The Hawaiian Monk Seal is the focus of one of the most proactive marine mammal recovery programs in the world (Lowry et al. 2011). Historically, the primary focus of the species’ recovery program was to increase survival of juvenile and adult female seals in the NWHI. Important recovery efforts have included: 1) removing marine debris from entangled seals 2) cleaning up marine debris and toxic chemicals in the seal’s habitats; 3) minimizing human activities that could disturb seals; 4) mitigating shark predation of young pups through pup translocations and shark removals; 5) removing and translocating adult males to mitigate mortality associated with male aggression towards juveniles and females; 6) rehabilitating and releasing malnourished young seals and conservation translocations designed to improve juvenile survival; and 7) regulating fisheries to reduce the likelihood of direct and indirect interactions. Conservation efforts have had substantial impacts with up to 30% of the current Monk Seal population being alive today due to mitigation efforts targeted towards individual seals over more than 30 years (Harting et al. 2014).

Monk Seal conservation translocations have been conducted with a variety of objectives, including reducing shark predation and conspecific male aggression, stopping human–seal interactions, and taking advantage of regional differences in demographic patterns to improve survival (Baker et al. 2011b, Norris et al. 2017, Baker et al. 2020b).

Steps have been taken to guard against disease outbreaks that could decimate the population. Background surveys conducted on Hawaiian Monk Seals showed that they remain naïve (no detectable antibodies) to potential virus threats including morbillivirus (Littnan et al. 2006), which has been associated with marine mammal mass mortality events worldwide, and that has been detected in other species in Hawaii (West et al. 2013). Efforts to monitor population health are ongoing and a morbillivirus vaccination program initiated in 2016 has succeeded in vaccinating a large proportion of the Hawaiian monk seal population (Baker et al. 2017, Robinson et al. 2018). Vaccine and treatment options for toxoplasmosis are currently lacking. Nevertheless, ailing seals diagnosed with toxoplasmosis are provided with intensive medical care. Stakeholder engagement and public information campaigns have been developed to address the source (i.e. domestic cats) of Toxoplasma on the terrestrial landscape.

In 2014, The Marine Mammal Center opened Ke Kai Ola, a privately funded and managed rehabilitation facility, was constructed to support recovery efforts. Seals from across the archipelago that are sick, injured, emaciated, or otherwise in need of rehabilitation are cared for at this Hawaiian Monk Seal hospital. Forty-eight seals were successfully rehabilitated and released during 2014 to 2022.

Considerable effort has been spent on the recovery program to develop strategies to maintain population growth in the MHI, while mitigating human-seal interactions (Lowry et al. 2011). The program is currently working on strategies to prevent unwanted seal behaviors including fisheries interactions and animals conditioned to interact with people. A significant component of this work includes community engagement on how to avoid negative wildlife interactions.
Actions de conservation (6)Expert
  • 1_1Site/area protection
  • 1_2Resource & habitat protection
  • 2_1Site/area management
  • 3_2Species recovery
  • 4_3Awareness & communications
  • 5_4_3Sub-national level
Stress écologiques (15)Expert
  • 1_1Ecosystem conversion
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_3Indirect ecosystem effects
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_2Species disturbance
  • 2_2Species disturbance
  • 2_2Species disturbance
  • 2_2Species disturbance
  • 2_2Species disturbance
Priorités de recherche (6)Expert
  • 1_2Population size, distribution & trends
  • 1_3Life history & ecology
  • 1_5Threats
  • 1_6Actions
  • 2_2Area-based Management Plan
  • 3_1Population trends
Niche IUCN globaleExpert

Royaumes biogéographiques

Oceanian

Systèmes (terrestre/eau douce/marin)

TerrestrialMarine

Large Marine Ecosystems (LMEs)

Insular Pacific Hawaiian

Zones de pêche FAO

Pacific - northwestPacific - eastern central
Références bibliographiques (30)Expert
  1. IUCN. 2025. The IUCN Red List of Threatened Species. Version 2025-2. Available at: <a href="www.iucnredlist.org">www.iucnredlist.org</a>. (Accessed: 10 October 2025).
  2. Robinson, S. J., Amlin, A. and Barbieri, M. 2023. Toxoplasma gondii, threatens Hawaiian monk seals (<i>Neomonachus schauinslandi</i>) following heavy runoff events. <i>Journal of Wildlife Diseases</i> 59(1): 1-11.
  3. Baker, J. D., Barbieri, M. M., Johanos, T. C., Littnan, C. L., Bohlander, J. L., Kaufman, A. C., Harting, A. L., Farry, S. C. and Yoshinaga, C. H. 2020b. Conservation translocations of Hawaiian monk seals: accounting for variability in body condition improves evaluation of translocation efficacy. <i>Animal Conservation</i> 24: 206-212.
  4. Baker, J. D., Harting, A. L., Johanos, T. C., London, J. M., Barbieri, M. M. and Littnan, C. L. 2020a. Terrestrial habitat loss and the long-term viability of the French Frigate Shoals Hawaiian monk seal subpopulation. U.S. Dept. of Commerce, NOAA Technical Memorandum NOAA-TM-NMFS- PIFSC-107.
  5. Robinson, S. J., Harting, A. L., Mercer, T., Johanos, T. C., Baker, J. D. and Littnan, C. L. 2020. Sighting patterns reveal unobserved pupping events to revise reproductive rate estimates for Hawaiian monk seals in the main Hawaiian Islands. <i>Marine Mammal Science</i> 37(2): 420-432.
  6. Rule, J.P., Adams, J.W., Marx, F.G., Evans, A.R., Tennyson, A.J.D., Scofield, R.P. and Fitzgerald, E.M.G. 2020. First monk seal from the Southern Hemisphere rewrites the evolutionary history of true seals. <i>Proceedings of the Royal Society B</i> 287: 20202318.
  7. Harting, A. L., Barbieri, M. M., Baker, J. D., Mercer, T. A., Johanos, T. C., Robinson, S. J., Littnan, C. L., Colegrove, K. M. and Rotstein, D. 2020. Population-level impacts of natural and anthropogenic causes-of-death for Hawaiian monk seals in the main Hawaiian Islands. <i>Marine Mammal Science</i> 37: 235-250.
  8. Robinson, S. J., Barbieri, M. M., Murphy, S., Baker, J. D., Harting, A. L., Craft, M. E. and Littnan, C. L. 2018. Model recommendations meet management reality: implementation and evaluation of a network-informed vaccination effort for endangered Hawaiian monk seals. <i>Proceedings of the Royal Society B </i> 285: 20171899.
  9. Wilson, K., Littnan, C. and Read, A. 2017b. Movements and home ranges of monk seals in the main Hawaiian Islands. <i>Marine Mammal Science</i> 33: 1080-1096.
  10. Wilson, K., Littnan, C., Halpin, P. and Read, A. 2017a. Integrating multiple technologies to understand the foraging behaviour of Hawaiian monk seals. <i>Royal Society Open Science </i> 4: 160703.
  11. Norris, T. A., Littnan, C. L., Gulland, F. M. D., Baker, J. D. and Harvey, J. T. 2017. An integrated approach for assessing translocation as an effective conservation tool for Hawaiian monk seals. <i>Endangered Species Research</i> 32: 103-115.
  12. Mohr, D. W., Naguib, A., Weisenfeld, N., Kumar, V., Shah, P., Church, D. M., Jaffe, D. and Scott , A. F. 2017. Improved de novo genome assembly: Linked-Read sequencing combined with optical mapping produce a high quality mammalian genome at relatively low cost. <i>BioRxiv </i>: 128348.
  13. Gobush, K., Wurth, T., Henderson, J., Becker, B. and Littnan, C. 2017. Prevalence of interactions between Hawaiian monk seals (<i>Neomonachus schauinslandi</i>) and nearshore fisheries in the main Hawaiian Islands. <i>Pacific Conservation Biology</i> 23: 25-31.
  14. Baker, J. D., Harting, A. L., Barbieri, M. M., Robinson, S. J., Gulland, F. M. and Littnan, C. 2017. Modeling a Morbillivirus Outbreak in Hawaiian Monk Seals to Aid in the Design of Mitigation Programs. <i>Journal of Wildlife Diseases</i> 53: 736-748.
  15. Barbieri, M. M., Kashinsky, L., Rotstein, D. S., Colegrove, K. M., Haman, K. H., Magargal, S. L., Sweeny, A. R., Kaufman, A. C., Grigg, M. E. and Littnan, C. L. 2016. Protozoal-related mortalities in endangered Hawaiian monk seals <i>Neomonachus schauinslandi</i>. <i>Diseases of Aquatic Organisms </i> 121: 85-95.
  16. Baker, J. D., Harting, A. L., Johanos, T. C. and Littnan, C. L. 2016. Estimating Hawaiian monk seal range-wide abundance and associated uncertainty. <i>Endangered Species Research </i> 31: 317-324.
  17. Harting A.L., Johanos T.C. and Littnan C.L. 2014. Benefits derived from opportunistic survival-enhancing interventions for the Hawaiian monk seal: the silver BB paradigm. <i>Endangered Species Research </i> 25: 89-96.
  18. Scheel D.M., Slater G.J., Kolokotronis S-O., Potter C.W., Rotstein D.S., Tsangaras K., Greenwood, A.D. and Helgen, K.M. 2014. Biogeography and taxonomy of extinct and endangered monk seals illuminated by ancient DNA and skull morphology. <i>ZooKeys </i> 409: 1-33.
  19. West, K.L., Sanchez, S., Rotstein, D., Robertson, K.M., Dennison, S., Levine, G., Davis, N., Schofield, D., Potter, C.W. and Jensen, B. 2013. A Longman's beaked whale (<i>Indopacetus pacificus</i>) strands in Maui, Hawaii, with first case of morbillivirus in the central Pacific. <i>Marine Mammal Science</i> 29: 767-776.
  20. Carretta, J.V., Oleson, E., Weller, D.W., Lang, A.R., Forney, K.A., Baker, J., Hanson, B., Martien, M., Muto, M.M., Lowry, M.S., Barlow, J., Lynch, D., Carswell, L., Brownell, R.L. Jr., Mattila, D.K. and Hill, M.C. 2013. U.S. Pacific Marine Mammal Stock Assessments: 2012. U.S. Department of Commerce, NOAA Technical Memorandum, NMFS-SWFSC-504. US Department of Commerce, National Oceanic and Atmospheric Administration, National Marine Fisheries Service, Southwest Fisheries Science Center.
  21. Cahoon, M.K., Littnan, C.L., Longenecker, K. and Carpenter, J.R. 2013. Dietary comparison of two Hawaiian monk seal populations: the role of diet as a driver of divergent population trends. <i>Endangered Species Research</i> 20: 137-146.
  22. US Census Bureau. 2012. Statistical Abstract of the United States: 2012 (131st Edition). US Census Bureau, Washington, D.C.
  23. Reynolds, M.H., Berkowitz, P., Courtot, K.N., Krause, C.M. 2012. Predicting sea-level rise vulnerability of terrestrial habitat and wildlife of the Northwestern Hawaiian Islands. U.S. Geological Survey Open-File Report 2012–1182.
  24. Baker, J. D., Becker, B. L., Wurth, T. A., Johanos, T. C., Littnan, C. L. and Henderson, J. R. 2011b. Translocation as a tool for conservation of the Hawaiian monk seal. <i>Biological Conservation</i> 144: 2692-2701.
  25. Baker, J.D., Harting, A.L., Wurth, T.A., Johanos, T.C. 2011a. Dramatic shifts in Hawaiian monk seal distribution and abundance are predicted to result from divergent regional trends. <i>Marine Mammal Science</i> 27: 78-93.
  26. Iverson, S., Piche, J. and Blanchard W. 2011. Hawaiian monk seals and their prey: assessing characteristics of prey species fatty acid signatures and consequences for estimating monk seal diets using fatty acid signature analysis. U.S. Department of Commerce, NOAA Technical Memorandum NOAA-TM-NMFS-PIFSC-23.
  27. Lowry, L.F., Laist, D.W., Gilmartin, W.G. and Antonelis, G.A. 2011. Recovery of the Hawaiian monk seal (Monachus schauinslandi): a review of conservation efforts, 1972 to 2010, and thoughts for the future. <i>Aquatic Mammals </i> 37: 397-419.
  28. Schultz, J.K., Baker, J.D., Toonen, R.J., Harting, A.L. and Bowen, B.W. 2011. Range-wide genetic connectivity of the Hawaiian monk seal and implications for translocation. <i>Conservation Biology</i> 25(1): 124-132.
  29. Schultz, J.K., Marshall, A.J. and Pfunder, M. 2010. Genome-wide loss of diversity in the critically endangered Hawaiian monk seal. <i>Diversity</i> 2: 863-880.
  30. Johanos T.C., Becker B.L., Baker J.D., Ragen T.J., Gilmartin W.G. and Gerrodette T. 2010. Impacts of sex ratio reduction on male aggression in the Critically Endangered Hawaiian monk seal <i>Monachus schauinslandi</i>. <i>Endangered Species Research </i> 11: 123-132.
Évaluateurs & contributeurs (4)Expert
assessor
Baker, J., Robinson, S., Harting, A., Barbieri, M. & Littnan, C.
contributor
Aguilar, A.
evaluator
Karamanlidis, A.A. & Kovacs, K.M.
facilitators
Battistoni, A.

Baker, J., Robinson, S., Harting, A., Barbieri, M. & Littnan, C. 2025. Neomonachus schauinslandi. The IUCN Red List of Threatened Species 2025: e.T13654A272355581. Accessed on 05 May 2026.

Traits biologiques

21 valeurs · 8 sources

Morphologie(5)

Masse adulte
223 kg
AnAge
Masse cerveau
370 g
AnimalTraits
Masse naissance
17 kg
AnAge
Masse au sevrage
64 kg
AnAge
Longueur
2,2 m
PanTHERIA

Cycle de vie(1)

Longévité max
30 ans
PanTHERIA
Voir 15 traits de plus (2 catégories)

Reproduction(6)

Sevrage
1,1 mois
AnAge
Taille de portée
1
AnAge
Portées par an
1
AnAge
Maturité sexuelle
5 ans
AnAge
Gestation
11 mois
AnAge
Intervalle naissances
1,3 ans
AnAge

Écologie & habitat(9)

Invertébrés (%)
30 %
elton_mammals
Graines (%)
0 %
elton_mammals
Fruits (%)
0 %
elton_mammals
Nectar (%)
0 %
elton_mammals
Charognard (%)
0 %
elton_mammals
Poissons (%)
70 %
elton_mammals
Autre végétal (%)
0 %
elton_mammals
Vert. ectothermes (%)
0 %
elton_mammals
Vert. endothermes (%)
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

Aucune observation géoréférencée avec précision suffisante (<10 km) dans GBIF pour cette espèce.

Consulter sur les bases externes

Observations & statuts

Cartographie

Bibliographie

Note nomenclaturale & synonymesExpert

Note nomenclaturale

TAXREF v18 — INPN/MNHN

Synonymes (2)— redirigent vers cette page

  • Monachus schauinslandiMatschie, 1905
  • Neomonachus schaunslandi(Matschie, 1905)

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