Ontologia
Platypus

Platypus

Ornithorhynchus anatinus(Shaw, 1799)

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

Description

espèce de mammifères du genre Ornithorhynchus

Source : Wikidata

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 Ornithorhynchus anatinus 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

45 partenaires écologiques documentés directement dans GloBI.

Partenaires
45
Espèces avec interactions documentées
Types d'interactions
5
Prédation, pollinisation, parasitisme…
Connectance
0.071
Densité des liens dans le sous-graphe affiché
Rang animalia
92 %
Percentile vs ensemble des animalia

Liste rouge IUCN

NT · Quasi menacéeDécroissante
Évaluation complète
Évaluation
2016 · v3.1
Altitude
m
Profondeur
m
État de la populationExpert

Difficulties in reliably quantifying platypus abundance compromise estimation of population size and its trends (Gust and Griffiths 2009). There has been no robust assessment of the population size of the Platypus either nationwide or for the key states in the species’ geographic range. Lunney et al. (2008) stated that ‘It is a common species’, but noted that ‘in general there is a surprising lack of knowledge about its abundance’. Carrick et al. (2008) considered it ‘common (though rarely abundant)’ but regarded it as ‘potentially vulnerable due to its specialised dependence on established water bodies for food and shelter’. Grant and Temple-Smith (2003) noted that the current and future conservation status of the Platypus is not easily predicted since their abundance is not readily measured. Since abundance is difficult to determine, population trends are generally poorly defined and the impacts of particular threats have been suggested and inferred, but rarely rigorously demonstrated (Gust and Griffiths 2009).

However, there have been some estimates of the number of individuals or of density for (parts of) individual rivers and for some areas. For Kangaroo Island, the size of the introduced subpopulation has been robustly estimated to be about 110 individuals (Furlan et al. 2012), with an effective population size of 11 individuals: this subpopulation was derived from a small number of individuals introduced between 1928 and the 1940s.

Platypus population densities in two reliably perennial rural streams in southern Victoria ranged from 1.3-2.1 subadults and adults per kilometre of channel (Serena 1994; Gardner and Serena 1995). In streams in high quality native forests at Lake Eildon National Park in central Victoria, densities were only 0.1-0.3 subadults and adults recorded per kilometre of perennial stream channel (Serena et al. 2001a, b). In a Tasmanian study of one catchment, catch rates were lower in headwaters than downstream reaches and in areas exposed to previous logging than in unmodified areas (Koch et al. 2006).

The extent of knowledge of population trends, and the trends themselves, have varied across its range. There is little available information on trends in Queensland. In New South Wales, Dickman (1994) noted that it had ‘declined in all regions’; and some studies have demonstrated local declines or even disappearances in recent decades (e.g. Grant and Denny 1991; Grant 1992, 1993, 1998; Rohweder 1992, Rohweder and Baverstock 1999; Lunney et al. 2008; Serena and Williams 2010d). A state-wide survey in 1987-88 concluded that its overall distribution had not changed significantly since the 1950s (Grant and Denny 1991; Grant 1992), and this pattern was broadly evident in some subsequent broad-scale assessment in 1994-96 (Grant et al. 2000). A more detailed and systematic assessment was undertaken in 2006, based on community knowledge (D. Lunney pers. comm. 2013). This concluded that there had been no sharp overall decline, but there were more locations showing decline than increase.

In Victoria, the Platypus is faring far less well, with substantial declines over recent decades. Mark-recapture studies carried out along the Wimmera River and its tributaries indicated that this system (conservatively estimated to have supported >1,500 Platypus at the time of European settlement) supported fewer than 200 individuals by the late 1990s, with numbers declining to <30 individuals by 2007 (Serena and Williams 2007b); juveniles have not been recorded in this system since 2006 (Griffiths and Weeks 2012). Capture frequency in replicated surveys in the Coliban River in central Victoria declined five-fold from 2001 to 2010, presumably due to drought (Williams 2010). It has been lost from several largely self-contained catchments, including the Cardinia Creek system in the mid-1980s (Serena and Williams 2004), the Curdies River system in the mid-1990s (Serena et al. 2002), and the Bass and Avoca River systems in the mid-2000s (Serena and Williams 2007a; M. Serena pers. comm. 2014). In the greater Melbourne area (across four hydrologically independent drainage basins) numerous subpopulations have contracted or become fragmented since 1995 as a by-product of urban or agricultural development and these are continuing to decline (Serena and Williams 2008a; Griffiths et al. 2012). Elsewhere in Victoria, both reduced flow regimes and severe flooding have contributed to the local depletion or disappearance of Platypus subpopulations (e.g. Serena and Williams 2007b, 2008b, 2010c).

There is little information on recent population trends in South Australia (Kangaroo Island). In Tasmania, trapping surveys in 2008-09 indicated that it remains widespread (Geragthy et al. 2011) and occupies a diverse array of water bodies (Gust et al. 2009). The lack of evidence for major reductions in abundance or distribution across Tasmania should be treated cautiously given the insensitivity of existing measures to detect change, the lack of systematic, rigorous monitoring for the species, and the possibility that significant localised declines occurred but went unnoticed (Gust and Griffiths 2010). 

Menaces identifiées(14 menaces classées CMP-IUCN)

  • 11_2
    Droughts
    Rapid DeclinesMajority (50-90%)Ongoing
  • 11_4
    Storms & flooding
    Rapid DeclinesMinority (<50%)Ongoing
  • 1_1
    Housing & urban areas
    Slow, Significant DeclinesMinority (<50%)Ongoing
  • 7_2_11
    Dams (size unknown)
    Slow, Significant DeclinesMinority (<50%)Ongoing
  • 8_1_1
    Unspecified species
    Slow, Significant DeclinesMajority (50-90%)Ongoing
  • 8_1_2
    Named species
    Slow, Significant DeclinesMajority (50-90%)Ongoing
  • 8_1_2
    Named species
    Slow, Significant DeclinesMajority (50-90%)Ongoing
  • 8_1_2
    Named species
    Slow, Significant DeclinesMajority (50-90%)Ongoing
  • 9_1_3
    Type Unknown/Unrecorded
    Slow, Significant DeclinesMajority (50-90%)Ongoing
  • 9_2_3
    Type Unknown/Unrecorded
    Slow, Significant DeclinesMinority (<50%)Ongoing

+ 4 menaces supplémentaires

Description complète des menacesExpert
Currently, the predominant threat to the species on the mainland is reduction in stream and river flows due to recent successive droughts, stream regulation, and extraction of water for agricultural, domestic, and industrial supplies. It is also at risk from the opposite extremes associated with climate change – extensive flooding both in space and time associated with recent tropical cyclones that have resulted in increased mortality and all but eliminated recruitment in 2006 over a substantial part of the species’ northern range. Habitat modification due to bank erosion and stream sedimentation (as a result of poor land management practices in agriculture, forestry, and urbanization) are also of great concern. In the case of urban streams, Platypus populations may be adversely affected by poor water quality (in the form of suspended solids and nutrient enrichment), contamination of sediment by heavy metals (Serena and Pettigrove 2005) and entanglement in or ingestion of plastic, rubber and metal litter. Accidental drowning in nets and traps set for fish and crustaceans has the potential to impact Platypus distribution and abundance in all parts of its range, especially in small streams where populations may be critically small. Populations in Tasmania are affected by mucormycosis (associated with the fungal pathogen Mucor amphibiorum) (Obendorf et al. 1993). Across its range, the Platypus is also subject to predation by the introduced Red Fox, dogs and cats.

Habitats préférentiels (classification IUCN)

  • 5_1Wetlands (inland) - Permanent Rivers/Streams/Creeks (includes waterfalls)
Mesures de conservation recommandéesExpert
Conservation of the Platypus is limited to its listing as a legally protected species in all states in which it occurs and its incidental inclusion in some national parks and reserves. Legislation prohibiting or controlling problematic fishing activities has been enacted in New South Wales and Victoria, but regulations concerning illegal netting and trapping are often poorly enforced. The most widespread field monitoring program for the species is in Victoria (Australian Platypus Conservancy). There are also a few system-specific studies in other states and community-based reporting of anecdotal occurrences of the species to a variety of institutional and private databases. Still more information about population numbers and monitoring are crucial, especially for a long-lived species such as the Platypus where a lack of recruitment can be masked until a dramatic population crash occurs as adults reach the end of their lifespan.

Population studies of fragmented populations should be a research priority, together with studies to help verify the current distribution and baseline population parameters in areas where the species has declined (Grant and Temple-Smith 2003). Once the Platypus becomes extinct in a river system, the likelihood of its re-colonising that system without human intervention is minimal (T. Grant, S. Munks, F. Carrick, and M. Serena pers. comm. 2014). One reintroduction program is underway in a single fire-affected stream in Victoria (Australian Platypus Conservancy).

Some populations of Platypuses have exhibited antibodies to Leptospirosis, probably transmitted via cattle, but no clinical symptoms have been observed. Mortality from an ulcerative dermatitis caused by Mucor fungus, however, has been recorded across many river systems in Tasmania. There is currently limited investigation of this disease, which should be a research priority both in that state and on the mainland where the fungus is also found (T. Grant, S. Munks, F. Carrick, and M. Serena pers. comm. 2014).
Actions de conservation (5)Expert
  • 1_2Resource & habitat protection
  • 2_1Site/area management
  • 2_2Invasive/problematic species control
  • 2_3Habitat & natural process restoration
  • 3_2Species recovery
Stress écologiques (18)Expert
  • 1_1Ecosystem conversion
  • 1_1Ecosystem conversion
  • 1_1Ecosystem conversion
  • 1_1Ecosystem conversion
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_2Species disturbance
Usage & commerce (1)Expert
  • 10Wearing apparel, accessories
    nationalsubsistance
Priorités de recherche (4)Expert
  • 1_2Population size, distribution & trends
  • 1_3Life history & ecology
  • 1_5Threats
  • 3_1Population trends
Niche IUCN globaleExpert

Royaumes biogéographiques

Australasian

Systèmes (terrestre/eau douce/marin)

TerrestrialFreshwater (=Inland waters)
Références bibliographiques (30)Expert
  1. 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).
  2. Woinarski, J.C.Z., Burbidge, A.A. and Harrison, P.L. 2014. <i>Action Plan for Australian Mammals</i>. CSIRO Publishing, Collingwood, Victoria.
  3. Griffiths, J., and Weeks, A. 2012. Distribution and relative abundance of platypuses in the Mackenzie River: survey results 2011/12. Report to Wimmera Catchment Management Authority. CESAR, Parkville.
  4. Furlan, E., Stoklosa, J., Griffiths, J., Gust, N., Ellis, R., Huggins, R. M., and Weeks, A. R. 2012. Small population size and extremely low levels of genetic diversity in island populations of the platypus, <i>Ornithorhynchus anatinus</i>. <i>Ecology and Evolution </i> 2: 844-857.
  5. Griffiths, J., Kelly, T., and Weeks, A. 2012. Distribution and relative abundance of platypuses in the greater Melbourne area: survey results 2011/12. Report to Melbourne Water. CESAR, Parkville.
  6. Geraghty, D. P., Griffiths, J., Stewart, N., Robertson, I. K., and Gust, N. 2011. Hematological, plasma, biochemical, and other indicators of the health of Tasmanian platypuses (<i>Ornithorhynchus anatinus</i>): predictors of mucormycosis. <i>Journal of Wildlife Diseases </i> 47: 483-493.
  7. Gust, N., and Griffiths, J. 2010. Tasmanian Platypus management plan. State of Tasmania, Biodiversity Conservation Branch. Department of Primary Industries, Parks, Water and Environment, Hobart.
  8. Serena, M., and Williams, G. 2010. Factors contributing to platypus mortality in Victoria. <i>The Victorian Naturalist</i> 127: 178-183.
  9. Serena, M., and Williams, G. A. 2010. Platypus population assessment and recommended management actions along Broken Creek. Report to Goulburn Broken Catchment Management Authority. Australian Platypus Conservancy, Wiseleigh.
  10. Williams, G. A. 2010. Results of a platypus live-trapping survey along the Coliban River, Malmsbury, October 2010. Report to North Central Catchment Management Agency. Australian Platypus Conservancy, Wiseleigh.
  11. Serena, M., and Williams, G. A. 2010. Platypus sightings records for the Murray River upstream of Lake Hume and its tributaries, 2009-2010. Report to Upper Murray Landcare Network. Australian Platypus Conservancy, Wiseleigh.
  12. Serena, M., and Williams, G. A. 2010. Conserving Platypus and water-rats: information and guidelines. Australian Platypus Conservancy, Wiseleigh.
  13. Gust, N., and Griffiths, J. 2009. Platypus mucormycosis and its conservation implications. <i>Australasian Mycologist</i> 28: 1-8.
  14. Gust, N., Griffiths, J., Driessen, M., Philips, A., Stewart, N., and Geraghty, D. 2009. Distribution, prevalence and persistence of mucormycosis in Tasmanian platypuses (<i>Ornithorhynchus anatinus</i>). <i>Australian Journal of Zoology</i> 57: 245-254.
  15. Lunney, D., Dickman, C., Copley, P., Grant, T., Munks, S., Carrick, F., Serena, M., and Ellis, M. 2008. <i>Ornithorhynchus anatinus</i>. In 'The IUCN Red List of Threatened Species'. Version 2012.2. Available at: <a href="www.iucnredlist.org">www.iucnredlist.org</a>. (Accessed: 4 November 2012).
  16. Serena, M., and Williams, G. A. 2008. The status of platypus in flood- and fire-affected catchments in Gippsland, 2008. Report to Victorian Department of Sustainability and Environment and Parks Victoria. Australian Platypus Conservancy, Wiseleigh.
  17. Carrick, F. N., Grant, T. R. and Temple-Smith, P. D. 2008. Platypus, <i>Ornithorhynchus anatinus</i>. In: S. Van Dyck and R. Strahan (eds), <i>The mammals of Australia. Third Edition</i>, pp. 32-35. Reed New Holland, Sydney, Australia.
  18. Serena, M., and Williams, G. A. 2008. Distribution and management of platypus in the greater Melbourne region. Report to Melbourne Water. Australian Platypus Conservancy, Wiseleigh.
  19. Serena, M., and Williams, G. 2007. Summary of recent platypus sightings and related information for the Melbourne Water extended area of operations. Report to Melbourne Water. Australian Platypus Conservancy, Wiseleigh.
  20. Serena, M., and Williams, G. A. 2007. Wimmera platypus conservation manual. Report to Wimmera Catchment Management Authority. Australian Platypus Conservancy, Wiseleigh.
  21. Koch, N., Munks, S. A., Utesch, M., Davies, P. E., and McIntosh, P. D. 2006. The platypus <i>Ornithorhynchus anatinus</i> in headwater streams, and effects of pre-Code forest clearfelling, in the South Esk River catchment, Tasmania, Australia. <i>Australian Zoologist </i> 33: 458-473.
  22. Serena, M. and Pettigrove, V. 2005. Relationship of sediment toxicants and water quality to the distribution of platypus populations in urban streams. <i>Journal of the North American Benthological Society</i> 24: 679-689.
  23. Serena, M., and Williams, G. A. 2004. An experimental reintroduction of platypus (<i>Ornithorhynchus anatinus</i>) to Cardinia Creek (April-June 2004). Report to Melbourne Water. Australian Platypus Conservancy, Whittlesea.
  24. Grant, T. R. and Temple-Smith, P. D. 2003. Conservation of the platypus, <i>Ornithorhynchus anatinus</i>: Threats and challenges. <i>Aquatic Health and Management</i> 6: 1-15.
  25. Serena, M., Williams, G. A., and Johnston, L. D. 2002. Status of platypus in the Curdies River catchment: live-trapping surveys and local sightings, summer 2002. Report to Corangamite Catchment Management Authority, Whittlesea.
  26. Serena, M., Williams, G. A., Swinnerton, M. 2001. Results of platypus population surveys in the Taponga River catchment, May 2001. Report to the Victorian Department of Natural resources and Environment. Australian Platypus Conservancy, Whittlesea.
  27. Serena, M., Worley, M., Swinnerton, M. and Williams, G. A. 2001. Effect of food availability and habitat on the distribution of platypus (Ornithorhynchus anatinus) foraging activity. <i>Australian Journal of Zoology</i> 49: 263-277.
  28. Grant, T. R., Gehrke, P. C., Harris, J. H., and Hartley, S. 2000. Distribution of the platypus (<i>Ornithorhynchus anatinus</i>) in New South Wales: Results of the 1994-1996 New South Wales Rivers Survey. <i>Australian Mammalogy </i> 21: 177-184.
  29. Rohweder, D. A. and Baverstock, P. R. 1999. Distribution of platypus, <i>Ornithorhynchus anatinus</i>, in the Richmond River Catchment, northern New South Wales. <i>Australian Zoologist </i> 31: 30-37.
  30. Grant, T. R. 1998. Current and historical occurrence of platypuses (<i>Ornithorhynchus anatinus</i>) around Sydney. <i>Australian Mammalogy</i> 20: 257-266.
Évaluateurs & contributeurs (3)Expert
assessor
Woinarski, J. & Burbidge, A.A.
contributor
Menkhorst, P., Grant, T., Dickman, C., Lunney, D., Serena, M., Gust, N. & Copley, P.
evaluator
Hawkins, C.

Woinarski, J. & Burbidge, A.A. 2016. Ornithorhynchus anatinus. The IUCN Red List of Threatened Species 2016: e.T40488A21964009. Accessed on 05 May 2026.

Traits biologiques

22 valeurs · 7 sources

Morphologie(4)

Masse adulte
1,25 kg
AnAge
Longueur
41,9 cm
PanTHERIA
Masse naissance
-999000 mg
PanTHERIA
Masse au sevrage
-999000 mg
PanTHERIA

Cycle de vie(1)

Longévité max
23 ans
AnAge
Voir 17 traits de plus (3 catégories)

Reproduction(6)

Sevrage
3,5 mois
AnAge
Taille de portée
2
AnAge
Maturité sexuelle
1,5 ans
AnAge
Portées par an
-999
PanTHERIA
Gestation
2,4 sem.
AnAge
Intervalle naissances
1 ans
AnAge

Écologie & habitat(9)

Invertébrés (%)
80 %
elton_mammals
Graines (%)
0 %
elton_mammals
Fruits (%)
0 %
elton_mammals
Nectar (%)
0 %
elton_mammals
Charognard (%)
0 %
elton_mammals
Poissons (%)
20 %
elton_mammals
Autre végétal (%)
0 %
elton_mammals
Vert. ectothermes (%)
0 %
elton_mammals
Vert. endothermes (%)
0 %
elton_mammals

Divers(2)

Taux métabolique
2.66 W
AnimalTraits
Température corporelle
34 °C
AnAge

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 (3)— redirigent vers cette page

  • Ornithorhynchus fuscusPeron
  • Ornithorhynchus rufusPeron
  • Platypus anatinusShaw, 1799

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