Ontologia
Phoque commun

Phoque commun

Phoca vitulinaLinnaeus, 1758

LCLR Monde (IUCN)
  1. Animal
  2. Chordata
  3. Mammalia
  4. Carnivora
  5. Phocidae
4 photos · 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 Phoca vitulina 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

144 partenaires écologiques documentés directement dans GloBI.

Partenaires
144
Espèces avec interactions documentées
Types d'interactions
7
Prédation, pollinisation, parasitisme…
Connectance
0.067
Densité des liens dans le sous-graphe affiché
Rang animalia
98 %
Percentile vs ensemble des animalia

Liste rouge IUCN

LC · Préoccupation mineure?Inconnue
Évaluation complète
Évaluation
2025 · v3.1
Altitude
03 m
Profondeur
4800 m
État de la populationExpert
The total population estimate for the area is around 130,000 individuals (Table 1; Banga et al. 2023, SCOS 2022, Galatius et al. 2022, Merkel et al. 2013, Nilssen et al. 2021, Nilssen and Bjørge 2019, Nilssen and Bjørge 2017a, 2017b, Hoekstein et al. 2022, Granquist 2021). The main (over 5,000 individuals) population centres are Scotland and the Wadden Sea (around 35,000 each), rest of Denmark and Sweden (c. 20,000 combined), Iceland (c. 15,000), Norway (10,000), England and Ireland (c. 5,000 each). Although overall the population in Europe has been recovering from historic hunting and bounty schemes, population trajectories vary even within metapopulations (Carroll et al. 2020) with increasing, stable and declining trends. Indeed, the following areas are showing evidence of depletion (since a baseline year of 1992) including Iceland, parts of Scotland (North Coast and Orkney, Shetland, Moray Firth, Eastern Scotland) and Northern Ireland (Thompson et al. 2019, Granquist 2021, Banga et al. 2023). Furthermore, although the current trend is unknown, abundance in Greenland is depleted compared to historic levels (1950s). There is also evidence of recent declines in Southeast England and the Dannish Kattegat (Banga et al. 2023, SCOS 22). Many of the current declines are due to unknown cause. The large Wadden Sea population appears to have reached carrying capacity around 2014 (Galatius et al. 2022).

Menaces identifiées(10 menaces classées CMP-IUCN)

  • 5_4_2
    Intentional use: (large scale) [harvest]
    Rapid DeclinesUnknownPast, Unlikely to Return
  • 5_4_4
    Unintentional effects: (large scale) [harvest]
    Rapid DeclinesUnknownOngoing
  • 11_1
    Habitat shifting & alteration
    UnknownUnknownOngoing
  • 5_4_1
    Intentional use: (subsistence/small scale) [harvest]
    UnknownUnknownOngoing
  • 5_4_5
    Persecution/control
    UnknownUnknownOngoing
  • 7_3
    Other ecosystem modifications
    UnknownUnknownFuture
  • 8_5_1
    Unspecified species
    UnknownUnknownOngoing
  • 9_2_3
    Type Unknown/Unrecorded
    UnknownUnknownOngoing
  • 9_4
    Garbage & solid waste
    UnknownUnknownOngoing
  • 9_6_3
    Noise pollution
    UnknownUnknownOngoing
Description complète des menacesExpert
There are a multitude of potential pressures on Harbour Seals (reviewed in Blanchet et al. 2021). The relatively large number of apparently closed, and in many cases small, subpopulations make the species vulnerable to range losses (Andersen and Olsen 2010). One of the most concerning aspects of Harbour Seal populations is their sudden and rapid decline with no obvious cause in some populations. This may be indicative of their susceptibility to multiple stressors. Current key potential threats incorporate both human activities and natural processes (disease, competition, and predation) which to some extent are mediated by current or historic human activities. 

Harbour Seals generally live in coastal areas and thus have considerable overlap with human activities. Historically their main threat was deliberate killing through hunting, culling and bounty schemes. Hunting is now only allowed in Norway and Sweden, where it is now licenced, and the numbers allowed to be killed are informed by population monitoring as part of a management plan. As such, the hunting should not be a long-term threat to population viability. In 2019 hunting was banned in Iceland and in 2020, the provision for killing of seals in the UK to protect fisheries was removed. Other current human activities that could impact Harbour Seals include fisheries, agriculture, shipping, oil and gas exploration, recreational activities and, most recently, renewable energy developments. It is difficult to attribute cause and impact on a population level and to date, evidence for population level impacts has been restricted to hunting, fisheries bycatch, and pollutants.  Bycatch in fisheries occurs throughout the majority of the range with likely population level impacts in some areas (Moan and Bjørge 2021). Historically, there have been relatively high levels of some environmental pollutants, including polychlorinated biphenyl (PCBs), found in Harbour Seals (Sonne et al. 2020) which have had population impacts (e.g. Wadden Sea; Reijnders 1986). As well as directly impacting reproduction, pollutants can cause vitamin deficiency (Brouwer et al. 1989) and immune system suppression (Ross et al. 1995, Desforges et al. 2016).

With the exception of direct killing, for most human activities, the impact on Harbour Seal vital rates and thus populations are unclear. Availability of haul-out sites can be impacted by developments and commercial kelp production but there is no indication that haul-out sites are limited within this area. Similarly, disturbance on haul-out sites could potentially impact numbers using local sites, but Harbour Seals appear to have some resilience to disturbance at haul-out sites (Paterson et al. 2019). Disturbance during breeding season is likely to be most problematic; it could lead to pup mortality through disruption of the mum-pup bond immediately after birth and thus pup abandonment. Harbour Seals are sensitive to noise disturbance at sea, and prevalence of such disturbance events are predicted to increase due to tidal and marine energy developments, and increased shipping. Although, small in number, tidal turbine arrays are typically inshore and Harbour Seals appear to favour such high current areas (Hastie et al. 2016). This has led to concerns regarding collision risk and population level impacts in some areas, but evidence so far indicates the noise of operational tidal turbines results in some avoidance (Onoufriou et al. 2021). Similarly, pile driving for wind farms has the potential to cause short-term displacement (Russell et al. 2016). The ramifications of such avoidance likely depend on the availability of other suitable foraging opportunities. Pile driving can potentially impact auditory range (Whyte et al. 2020); the level of exposure is likely mediated by a trade-off between the importance of the area and sound level (Hastie et al. 2020). The ramifications of decreased auditory range are not well understood but could impact reproductive behaviour.

Natural threats include disease epidemics, biotoxins, predation (by Killer Whales, Polar Bears, and Grey Seals) and competition for prey. Harbour Seals are susceptible to disease outbreaks; mass morality events have been caused by Phocine Distemper Virus in 1988 (estimated mortality of  over 23,000) and 2002 (over 30,000; Härkönen et al. 2006), and Avian influenza in 2014 (over 2,000; Zohari et al. 2014, Bodewes et al. 2015). Recent evidence shows that, at least in some areas, many important prey species have considerably high levels of biotoxins year-round, potentially leading to chronic exposure in seals and reduction of demographic rates (Kershaw et al. 2021). Grey Seals, which compete with, and in some cases prey on (van Neer et al. 2015) Harbour Seals, are increasing both in abundance and distribution particularly in the southern North Sea. Historically Grey Seal colonies were, for the most part, restricted to a limited number of offshore islands that lacked land predators while Harbour Seals could exploit tidal sandbanks. However, the lack of such predators, and more recently the cessation of human exploitation, has facilitated an increase in the Grey Seal population. In southeast England, Grey Seals are increasing at a rate of  over 10% per annum while recent Harbour Seal counts indicate a c. 20% drop in what was a stable population (SCOS 2022). In addition, Grey Seals are much more wide-ranging than Harbour Seals (e.g. the northeast Atlantic is believed to be a single subpopulation), and could act as transmission vectors for infectious diseases. The increase in Grey Seal numbers in the southern North Sea could increase competition for prey, increase predation, and facilitate or enhance the spread of diseases such as the next PDV epidemic that is predicted to be imminent. The impacts of climate change are likely to be complex and multi-faceted, acting both directly and directly. Harbour Seal haul-out patterns are impacted by weather, with time hauled out lower at both very cold (Routti et al. 2014) and hot temperatures (Hansen et al. 1997). In many parts of their range sea level rise will likely lead to loss of current haul out sites. The availability of newly created haul-out sites will in many places depend on local mitigation efforts such as flood defences. The reduction of ice in the Arctic is likely to be associated with increased anthropogenic activity and thus potential for disturbance and pollution. Climate change will result in changes in prey composition throughout most of their range and could potentially result in an increased prevalence of harmful algal blooms (HAB; Gobler 2020) events and the spread of disease (Harvell et al. 1999).

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
  • 12_3Marine Intertidal - Shingle and/or Pebble Shoreline and/or Beaches
  • 13_1Marine Coastal/Supratidal - Sea Cliffs and Rocky Offshore Islands
  • 9_1Marine Neritic - Pelagic
  • 9_10Marine Neritic - Estuaries
Mesures de conservation recommandéesExpert
Recent changes have effectively ended deliberate killing of Harbour Seals throughout most of the area. A ban on hunting is quite recent in some areas and thus the impact on populations may not have been realised (e.g. since 2010 and 2019 in Greenland and Iceland, respectively). Hunting is currently only permitted in Norway, though a Management Plan was implemented in 2010 which aims to maintain the population size (at a count of 7,000 individuals during the moult). Some hunting, under licence is permitted in Sweden. Shooting seals to fisheries has recently been banned in many countries including Norway (2019), Canada (2020), and UK (2020). In the UK such shooting was already restricted (in numbers and/or location) and it was unlikely to have contributed to any regional declines). As well as country level protections, there are specific conservation strategies on haul out specific level (e.g. Special Areas of Conservation in the European Union and the UK) to multi-country levels (e.g OSPAR). Harbour Seals are included in The Bern Convention, EU Habitats Directive, Convention on the Conservation of Migratory Species of Wild Animals (CMS; Baltic and Wadden Sea populations only), The Convention on the Protection of the Marine Environment of the Baltic Sea Area (Helsinki Convention, HELCOM) and the Agreement on the Conservation of Seals in the Wadden Sea, and their abundance and distribution are biodiversity indicators under OSPAR.

There are additional conservation measures which act on a regional or haul-out site level including Coastal Reserves in Norway which exclude commercial fishing (these have been shown to reduce harbour seal mortality), Seal Conservation Areas (Scotland), and designated haul-out sites (at which it is illegal to intentionally or recklessly harass seals; Scotland).

Further research into the population trends and threats faced by the species is recommended.
Actions de conservation (1)Expert
  • 2_1Site/area management
Stress écologiques (30)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_3Indirect ecosystem effects
  • 1_3Indirect ecosystem effects
  • 1_3Indirect ecosystem effects
  • 1_3Indirect ecosystem effects
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 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
  • 2_2Species disturbance
  • 2_2Species disturbance
  • 2_2Species disturbance
  • 2_2Species disturbance
Usage & commerce (2)Expert
  • 1Food - human
    subsistance
  • 10Wearing apparel, accessories
    subsistance
Priorités de recherche (5)Expert
  • 1_2Population size, distribution & trends
  • 1_4Harvest, use & livelihoods
  • 1_5Threats
  • 1_6Actions
  • 3_1Population trends
Niche IUCN globaleExpert

Royaumes biogéographiques

Palearctic

Systèmes (terrestre/eau douce/marin)

TerrestrialMarine

Large Marine Ecosystems (LMEs)

Barents SeaEast Greenland ShelfIceland ShelfNorth SeaNorwegian SeaCeltic-BiscayBaltic Sea

Zones de pêche FAO

Atlantic - northwestAtlantic - northeastPacific - northwestPacific - northeastPacific - eastern central
Références bibliographiques (30)Expert
  1. IUCN. 2025. The IUCN Red List of Threatened Species. Version 2025-1. Available at: <a href="www.iucnredlist.org">www.iucnredlist.org</a>. (Accessed: 27 March 2025).
  2. ICES. 2024. Working Group on Marine Mammal Ecology (WGMME). ICES Scientific Reports 6(8): 2239. https://doi.org/10.17895/ices.pub.26997367
  3. NAMMCO. 2024. HARBOUR SEAL. Helsinki. North Atlantic Marine Mammal Commission (NAMMCO). Available at: <a href="https://nammco.no/harbour-seal/#1670770907469-36a19759-f5c8">https://nammco.no/harbour-seal/#1670770907469-36a19759-f5c8</a>. (Accessed: 3 September 2024).
  4. Banga, R., Russell, D.J.F., Carter, M.I.D., Chaudry, F., Gilles, A., Abel, C., Ahola, M., Authier, M., Bjørge, A., Brasseur, S., Carlsson, A., Carlstrom, J., Christensen, A.H., Dinis, A., Engene, N., Galatius, A., Geelhoed, S., Granquist, S., Haelters, J., Jess, A., Morris, C., Murphy, S., Ó Cadhla, O., Persson, S., Pierce, G., Poncet, S., Rosing-Asvid, A., Saavedra, C., Taylor, N., Teixeira, A., van Neer, A., Vasconcelos, R. and Vincent, C. 2022. Seal Abundance and Distribution. In: OSPAR (ed.), <i>The 2023 Quality Status Report for the Northeast Atlantic</i>, OSPAR Commission, London.
  5. Hoekstein, M.S.J., Sluijter, M., van Straalen, K.D. 2022. Watervogels en zeezoogdieren in de Zoute Delta 2020/2021. <i>Rijkswaterstaat,Centrale informatievoorziening Deltamilieu Projecten, Vlissingen</i>.
  6. SCOS. 2022. Scientific advice on matters related to the management of seal populations. (in press).
  7. Kershaw, J.L., Jensen, S.-K., McConnell, B., Fraser, S., Cummings, C., Lacaze, J.-P., Hermann, G., Bresnan, E., Dean, K.J., Turner, A.D., Davidson, K. and Hall, A.J. 2021. Toxins from harmful algae in fish from Scottish coastal waters. <i>Harmful Algae</i> 105: 102068. https://doi.org/10.1016/j.hal.2021.102068
  8. Onoufriou, J., Russell, D.J., Thompson, D., Moss, S.E. and Hastie, G D. 2021. Quantifying the effects of tidal turbine array operations on the distribution of marine mammals: Implications for collision risk. <i>Renewable Energy</i> 180: 157-165.
  9. Moan, A. and Bjørge, A. 2021. Bycatch of coastal seals in Norwegian gillnet fisheries conducted by coastal fish-ing vessels. NAMMCO SC Working Group on Bycatch.
  10. Hastie, G.D., Lepper, P., McKnight, J.C., Milne, R., Russell, D.J. and Thompson, D. 2021. Acoustic risk balancing by marine mammals: anthropogenic noise can influence the foraging decisions by seals. <i>Journal of Applied Ecology</i> 58(9): 1854-1863.
  11. Blanchet, M.A., Vincent, C., Womble, J.N., Steingass, S.M. and Desportes, G. 2021. Harbour Seals: Population Structure, Status, and Threats in a Rapidly Changing Environment. <i>Oceans</i> 2: 41-63.
  12. Carroll, E.L., Hall, A., Olsen, M.T., Onoufriou, A.B., Gaggiotti, O.E. and Russell, D.J. 2020. Perturbation drives changing metapopulation dynamics in a top marine predator. <i> Proceedings of the Royal Society B</i> 287(1928): https://doi.org/10.1098/rspb.2020.0318.
  13. Whyte, K.F., Russell, D.J.F., Sparling, C.E., Binnerts, B., and Hastie, G.D. 2020. Estimating the effects of pile driving sounds on seals: Pitfalls and possibilities. <i>The Journal of the Acoustical Society of America</i> 147: 3948-3958.
  14. Gobler, C.J. 2020. Climate Change and Harmful Algal Blooms: Insights and perspective. <i>Harmful Algae</i> 91: 101731. DOI: 10.1016/j.hal.2019.101731.
  15. Sonne, C., Siebert, U., Gonnsen, K., Desforges, J.P., Eulaers, I., Persson, S., Roos, A., Bäcklin, B.-M., Kauhala, K., Olsen, M.T., Harding, K.C., Treu, G., Galatius, A., Anderson-Ranberg, E., Gross, S., Lakemeyer, J., Lehnert, K., Lam, S.S., Peng, W. and Dietz, R. 2020. Health effects from contaminant exposure in Baltic Sea birds and marine mammals: A review. <i>Environment international</i> 139: 105725. https://doi.org/10.1016/j.envint.2020.105725
  16. Nilssen K.T. and Bjørge A. 2019. Havforskningsrapporten 2017. Fisken og havet, særnr. Norway: Sjøpattedyrutvalget.
  17. Paterson, W.D., Russell, D.J., Wu, G.M., McConnell, B., Currie, J.I., McCafferty, D.J. and Thompson, D. 2019. Post-disturbance haulout behaviour of harbour seals. <i>Aquatic Conservation: Marine and Freshwater Ecosystems</i> 29(S1): 144–156. https://doi.org/10.1002/aqc.3092
  18. Wilson, L.J. and Hammond, P.S. 2019. The diet of harbour and grey seals around Britain: Examining the role of prey as a potential cause of harbour seal declines. <i>Aquatic Conservation: Marine and Freshwater Ecosystems</i> 29: 71-85.
  19. Nilssen, K.T. and Bjørge, A. 2017. Status for kystsel. Anbefaling av jaktkvoter for 2018. Norwegian Marine Mammal Scientific Advisory Board.
  20. Nilssen, K.T. and Bjørge, A. 2017. Havert og steinkobbe. In: I.E. Bakketeig, M. Hauge and C. Kvamme (eds), <i>Havforskningsrapporten 2017. Fisken og havet, særnr</i>, pp. 68–69.
  21. Hastie, G.D., Russell, D.J., Benjamins, S., Moss, S., Wilson, B. and Thompson, D. 2016. Dynamic habitat corridors for marine predators; intensive use of a coastal channel by harbour seals is modulated by tidal currents. <i>Behavioral Ecology and Sociobiology</i> 70: 2161-2174.
  22. Desforges, J.P.W., Sonne, C., Levin, M., Siebert, U., De Guise, S. and Dietz, R. 2016. Immunotoxic effects of environmental pollutants in marine mammals. <i>Environment International</i> 86: 126-139.
  23. Russell, D.J.F., Hastie, G.D., Thompson, D., Janik, V.M., Hammond, P.S., Scott-Hayward, L.A.S., Matthiopoulos, J., Jones, E.L. and McConnell, B.J. 2016. Avoidance of wind farms by harbour seals is limited to pile driving activities. <i>Journal of Applied Ecology</i> 53(6): 1642-1652.
  24. van Neer, A., Jensen, L. F. and Siebert, U. 2015. Grey seal (<i>Halichoerus grypus</i>) predation on harbour seals (<i>Phoca vitulina</i>) on the island of Helgoland, Germany. <i>Journal of Sea Research</i> 97: 1-4.
  25. Hastie, G. D., Russell, D.J.F., McConnell, B., Moss, S., Thompson, D. and Janik, V.M. 2015. Sound exposure in harbour seals during the installation of an offshore wind farm: predictions of auditory damage. <i>Journal of Applied Ecology</i> 52: 631-640.
  26. Routti, H., Lydersen, C., Hanssen, L. and Kovacs, K.M. 2014. Contaminant levels in the world’s northernmost harbor seals (<i>Phoca vitulina</i>). <i>Marine pollution bulletin</i> 87(1-2): 140-146.
  27. Zohari, S., Neimanis, A., Harkonen, T., Moraeus, C. and Valarcher, J.F. 2014. Avian influenza A(H10N7) virus involvement in mass mortality of harbour seals (<i>Phoca vitulina</i>) in Sweden, March through October 2014. <i>Eurosurveillance</i> 19(46): 20967. https://doi.org/10.2807/1560-7917.ES2014.19.46.20967
  28. Merkel, B., Lydersen, C., Yoccoz, N.G. and Kovacs, K.M. 2013. The World’s Northernmost Harbour Seal Population–How Many Are There? <i>PloS ONE</i> 8(7): e67576. https://doi.org/10.1371/journal.pone.0067576
  29. Peterson, S.H., Lance, M.M., Jeffries, S.J. and Acevedo-Gutiérrez, A. 2012. Long distance movements and disjunct spatial use of harbor seals (<i>Phoca vitulina</i>) in the inland waters of the Pacific Northwest. <i>PloS one</i> 7(6): e39046. https://doi.org/10.1371/journal.pone.0039046
  30. Skeate, E.R., Perrow, M.R. and Gilroy, J.J. 2012. Likely effects of construction of Scroby Sands offshore wind farm on a mixed population of harbour <i>Phoca vitulina</i> and grey <i>Halichoerus grypus</i> seals. <i>Marine Pollution Bulletin</i> 64: 872-881.
Évaluateurs & contributeurs (3)Expert
assessor
Russell, D.J.F.
contributor
Lowry, L., Ahonen, H., Chiozza, F., Pollock, C.M. & Battistoni, A.
evaluator
Bellotto, V.

Russell, D.J.F. 2025. Phoca vitulina (Europe assessment). The IUCN Red List of Threatened Species 2025: e.T17013A225215605. Accessed on 05 May 2026.

Traits biologiques

23 valeurs · 7 sources

Morphologie(5)

Masse adulte
27 kg
AnAge
Masse cerveau
274 g
AnimalTraits
Masse naissance
11 kg
AnAge
Masse au sevrage
23,9 kg
AnAge
Longueur
1,6 m
PanTHERIA

Cycle de vie(1)

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

Reproduction(6)

Sevrage
1 mois
AnAge
Taille de portée
1
AnAge
Maturité sexuelle
4 ans
AnAge
Portées par an
1
AnAge
Gestation
8,3 mois
AnAge
Intervalle naissances
1 ans
AnAge

Écologie & habitat(9)

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

Divers(2)

Taux métabolique
73.29 W
AnAge
Température corporelle
36,7 °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

Bibliographie