Ontologia
Phoque gris

Phoque gris

Halichoerus grypus(Fabricius, 1791)

LCLR Monde (IUCN)
  1. Animal
  2. Chordata
  3. Mammalia
  4. Carnivora
  5. Phocidae
1 photo · Licences CC (Wikimedia Commons / iNaturalist)Click pour agrandir

Description

espèce de mammifères

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 Halichoerus grypus 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

188 partenaires écologiques documentés directement dans GloBI.

Partenaires
188
Espèces avec interactions documentées
Types d'interactions
9
Prédation, pollinisation, parasitisme…
Connectance
0.067
Densité des liens dans le sous-graphe affiché
Rang animalia
99 %
Percentile vs ensemble des animalia

Liste rouge IUCN

LC · Préoccupation mineureCroissante
Évaluation complète
Évaluation
2025 · v3.1
Altitude
03 m
Profondeur
4120 m
État de la populationExpert
The centre of abundance of the Eastern Atlantic Grey Seals is around the UK. The main UK colonies are in Scotland’s Outer Hebrides, Orkney and Southeast England. There are also breeding colonies across the rest of the UK. Although the number of pups born has grown steadily throughout the UK, there is clear evidence that the population’s growth rate is levelling off in all areas except the central and southern North Sea where growth rates remain high. Grey Seal population trends in the UK are assessed from the counts of pups born during the autumn breeding season (Russell et al. 2019). The most recent (2019) estimate of Grey Seal pup production in the UK was 67,850 (95% CI 50,250-85,400; SCOS 2021). Pup production, along with scaled haul-out counts in August, are used to estimate total non-pup population size using a Bayesian state-space model resulting in an estimate of 140,700 (95% CI: 129,300-153,500) in 2020(SCOS 2021). 

The latest aerial census to estimate the status of the Grey Seal population in Iceland was conducted in 2017. The total population size was estimated to be 6269 (95% CI: 5375–7181) (Granquist and Hauksson 2019). A population modelling study has indicated an increase in abundance of the Norwegian Grey Seal population during the last 30 years, with a total of 8,740 (95% CI: 7,320–10,170) animals estimated in 2011 (Øigård et al. 2012, NAMMCO 2016). However, new boat-based surveys carried out in 2014–2015 did, indicated a significant decrease in the grey seal pup production compared with the counts in the period 2007–2008, likely due to high levels of by-catch in the monkfish fishery.

There is no current information on the abundance or trends in the number of grey seals in the White Sea. Grey seals are rapidly increasing in abundance in the Wadden Sea (Danish, German and Dutch coasts) with 9,069 during the moulting period in spring 2021 (Brasseur et al. 2021).

In France, the most recent data available was a count of 6,269 grey seals in 2021 (ICES 2022). Grey seals in the Baltic Sea are recovering after a century of bounty hunting and several decades of low fertility caused by environmental pollution (Harding et al. 2007). The population has continued to increase with 42,000 counted in 2021 (HELCOM EG MAMA).

Menaces identifiées(7 menaces classées CMP-IUCN)

  • 11_1
    Habitat shifting & alteration
    UnknownUnknownOngoing
  • 5_4_1
    Intentional use: (subsistence/small scale) [harvest]
    UnknownUnknownOngoing
  • 5_4_4
    Unintentional effects: (large scale) [harvest]
    UnknownUnknownOngoing
  • 5_4_5
    Persecution/control
    UnknownUnknownOngoing
  • 9_2_3
    Type Unknown/Unrecorded
    UnknownMinority (<50%)Ongoing
  • 9_3_4
    Type Unknown/Unrecorded
    UnknownMinority (<50%)Ongoing
  • 5_4_2
    Intentional use: (large scale) [harvest]
    Slow, Significant DeclinesUnknownPast, Unlikely to Return
Description complète des menacesExpert
Grey Seals have been important in subsistence harvests throughout the history of their contact with humans. They have been hunted by peoples of the Baltic Sea coast for more than 10,000 years (Harkonen et al. 2005). Overharvesting in the Baltic in the early 20th century led to a large decline, from a population that once numbered an estimated 30,000 to perhaps as high as 200,000 to a low of 1,500-2,000 by the early 1980s (Kokko et al. 1999).

Government culls, bounties, and licensed kills for harvest and protection of fishing gear have been put into effect in many countries (Bowen and Lidgard 2013), and continue to be used in some in efforts to control Grey Seal numbers and reduce their impact on commercially important fisheries. Grey Seals feed on some commercial species, and by damaging nets and traps, they are in direct conflict with fisheries. Grey Seals are the terminal vector for seal worm life cycle, also known as cod worm, a destructive parasite of groundfish, including Atlantic cod (Bowen 1990, ICES 2005). Offshore renewable construction and ongoing operation could influence Grey Seal feeding. Grey Seals exposed to pile driving noise off the coast of the Netherlands have shown changes in dive behaviour and possible avoidance behaviour (Aarts et al. 2018). These effects appear to be short term as seals returned to the same locations on later trips. Grey Seals have also been tracked swimming through operational wind farms with no indication of overt avoidance off both the UK and Danish coasts (Russell et al. 2016). Entanglement in commercial fishing nets causes bycatch mortality in most parts of the Grey Seals’ range (Woodley and Lavigne, 1991). Bycatch levels are approximately 300 per year in Swedish fisheries in the Baltic (ICES 2005). Estimated bycatch levels in the Western Channel and Celtic Sea exceed the potential biological removal level for the combined Grey Seal populations of SW England, Wales, and Ireland. An additional but unknown number of seals are bycaught by non-UK registered boats operating in the Celtic Sea. Despite the bycatch, Grey Seal populations in Wales and Ireland are increasing, suggesting that bycaught seals include animals that may have originated from larger Scottish breeding populations. Grey Seals are known carriers of the morbillivirus known as phocine distemper virus (PDV), in all populations (Ross et al. 1992, Duignan et al. 1995, Harkonen et al. 2006). However, they have suffered almost no mortality from the disease. Harkonen et al. (2006) report Grey Seal mortality of approximately 230 (equal to 1% of the harbour seal mortality) in the 1988 epizootic in Europe, and the death of 30 gray seal pups in the Baltic were attributed to PDV. Because Grey Seals haul out with harbour seals in the Wadden Sea and are known to travel more widely than the sedentary harbour seal, it is presumed that they had a role in the outbreak and spread of the 2002 epizootic of PDV in harbour seals.

As a coastal species, Grey Seals are exposed to and ingest industrial and agricultural pollutants through the food chain. PCBs and DDT contaminant loads are extremely high in Baltic Sea Grey Seals, even though tissue burdens have declined since the 1970s. Analysis of samples collected from 1996 to 1998 indicated that gray seals still have a very heavy load of contaminants when compared to other seals outside the Baltic (ICES 2005). Health effects on Grey Seals have been suggested to be linked to very high exposures of PCBs and DDT. Baltic Sea Grey Seals have a relatively high rate of colonic ulcers, sometimes fatal, associated with hookworm infestations. This condition occurs in the Baltic Sea ringed seals as well, but essentially not found elsewhere in either species (ICES 2005). Uterine stenosis and a range of pathologies in other organs have been attributed to long-term exposure to environmental toxins, particularly in older Baltic Sea gray seals. These are specifically linked to reproductive, and population declines for this subspecies, and are conditions not seen in other populations (Bergman et al. 2001). However, no negative effects have been attributed to heavy metal contaminants in the Baltic gray seals (Bergman et al. 2001, ICES 2005).

The potential effects of climate change, either warming or cooling, on Grey Seals are not well known. In the Western Atlantic subspecies, decreases in the amount of sea ice in the Gulf of St. Lawrence during the pupping season have led to a shift to land breeding and may have increased pup mortality (den Heyer et al. 2021). A shift in mean birthdate of almost two weeks at the Sable Island colony in the Western Atlantic has been associated with a warming trend and an increasing population (Bowen et al. 2020). None of the above is thought to be a major threat to the species at present.

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
  • 13_3Marine Coastal/Supratidal - Coastal Sand Dunes
  • 17Other
  • 9_1Marine Neritic - Pelagic
Mesures de conservation recommandéesExpert
Numerous countries have invoked protective measures to limit Grey Seal harvests, culls, disturbance, and by-catch (Bonner 1981, ICES 2005). In the UK, Grey Seals are protected under the Conservation of Seals Act 1970 (England, and Wales), the Marine (Scotland) Act 2010 and The Wildlife (Northern Ireland) Order 1985. Until recently permits to protect fishing and aquaculture operations from grey seals were required, however, the lethal removal of grey seals in defence of gear damage this provision has been removed from legislation (SCOS 2020). In the UK such shooting was already restricted (in numbers and/or location) and it was unlikely to have had impacts on population trends.

Special Areas of Conservation (SAC) set out under the European Union's Habitats Directive (92/43/EEC) have been established to support the conservation of grey seals throughout its range. Pollutant loads in Baltic grey seals have declined in step with regulations banning the use and/or discharge of toxic pollutants such as DDT and PCBs beginning in the 1970s, and the reproductive health of female Grey Seals has improved as has the population level in the Baltic (Bergman et al. 2001). The establishment of coastal marine reserves for seals in Norway has been more effective in protecting harbour seals than Grey Seals because the latter are more likely to travel outside the areas closed to fisheries and become entangled in nets (Bjore et al. 2002).
Actions de conservation (1)Expert
  • 2_1Site/area management
Stress écologiques (10)Expert
  • 1_1Ecosystem conversion
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_2Species disturbance
  • 2_3_8Other
Usage & commerce (2)Expert
  • 1Food - human
    subsistance
  • 10Wearing apparel, accessories
    subsistance
Priorités de recherche (4)Expert
  • 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 SeaScotian ShelfNewfoundland-Labrador ShelfNE US Continental ShelfNorth SeaNorwegian SeaCeltic-BiscayBaltic Sea

Zones de pêche FAO

Atlantic - northwestAtlantic - northeast
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. Brasseur, S. M., Abel, C., Galatius, A., Jeß, A., Körber, P., Meise, K., ... and Klöpper, S. 2021. EG-Marine Mammals grey seal surveys in the Wadden Sea and Helgoland in 2020-2021. In: Common Wadden Sea Secretariat (CWSS) (ed.). Wilhelmshaven, Germany.
  3. SCOS. 2020. Scientific Advice on Matters Related to the Management of Seal Populations: 2020. Natural Environment Research Council, Swiddon, UK.
  4. Russell, D. J. F., Morris, C. D., Duck, C. D., Thompson, D., Hiby, L. 2019. Monitoring long-term changes in UK grey seal pup production. <i>Aquatic Conservation-Marine and Freshwater Ecosystems </i> 29: 24-39.
  5. Granquist, S., Hauksson, E. 2019. Population estimate, trends and current status of the Icelandic harbour seal (<i>Phoca vitulina</i>) population in 2018. <i>Marine and Freshwater Research in Iceland. </i> HV(36).
  6. HELCOM. 2018. Baltic Sea trends - Population trends and abundance of seals. HELCOM core indicator report. HELCOM.
  7. SCOS. 2018. Scientific Advice on Matters Related to the Management of Seal Populations: 2018. Natural Environment Research Council, Swiddon, UK.
  8. NAMMCO. 2016. Report of the 23rd Meeting of the Scientific Committee. Pages 95-328 In: NAMMCO Annual Report 2016, NAMMCO, Tromsø, Norway.
  9. Bowen, W.D., den Heyer, C.E., McMillan, J.I., and Iverson S.J. 2015. Offspring size at weaning affects survival to recruitment and reproductive performance of primiparous gray seals. <i>Ecology and Evolution</i> 5: 1412-1424.
  10. Hammill, M.O., Stenson, G.B., Swain, D.P. and Benoit, H.P. 2014b. Feeding by grey seals on endangered stocks of Atlantic cod and white hake. <i>ICES Journal of Marine Science</i> 71: 1332-1341.
  11. Committee on Taxonomy. 2014. List of marine mammal species and subspecies. Society for Marine Mammalogy. Available at: <a href="https://www.marinemammalscience.org/species-information/list-of-marine-mammal-species-subspecies/">https://www.marinemammalscience.org/species-information/list-of-marine-mammal-species-subspecies/</a>. (Accessed: 4 February 2014).
  12. Waring G.T., Josephson E., Maze-Foley K., Rosel, P.E., editors. 2013. U.S. Atlantic and Gulf of Mexico Marine Mammal Stock Assessments, 2012. NOAA Technical Memorandum NMFS-NE-223. National Marine Fisheries Service, Woods Hole, MA.
  13. 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.
  14. Øigård, T.A., Frie, A.K., Nilssen, K.T. and Hammill, M.O. 2012. Modelling the abundance of grey seals (<i>Halichoerus grypus</i>) along the Norwegian coast. <i>ICES Journal of Marine Science</i> 69: 1436-1447.
  15. DFO. 2011. Stock assessment of Northwest Atlantic grey seals (<i>Halichoerus grypus</i>). Department of Fisheries and Oceans Canada Canadian Science Advisory Secretariat Science Advisory Report 2010/091.
  16. Sette, L.A., Waring, G.T., Touhey, K., Sharp, S., Sharp, B. and Landry, S. 2009. Photographic surveys of entanglement occurrence at grey seal (<i>Halichoerus grypus</i>) and harbor seal (<i>Phoca vitulina</i>) haul-outs on Cape Cod, Massachusetts. Poster presentation, 18th Biennial Conference on the Biology of Marine Mammals.
  17. Breed, G.A., Jonsen, I.D., Myers, R.A., Bowen, W.D. and Leonard, M.L. 2009. Sex-specific, seasonal foraging tactics of adult grey seals (<i>Halichoerus grypus</i>) revealed by state--space analysis. <i>Ecology</i> 90(11): 3209-3221.
  18. Noren, S.R., Boness, D.J., Iverson, S.J., McMillan, J. and Bowen W.D. 2008. Body condition at weaning affects the duration of the postweaning fast in gray seal pups (<i>Halichoerus grypus</i>). <i>Physiological and Biochemical Zoology</i> 81: 269-277.
  19. Jüssi, M., Härkönen, T., Jüssi, I. and Helle, E. 2008. Decreasing ice coverage will reduce the reproductive success of Baltic grey seal <i>(Halichoerus grypus)</i> females. <i>Ambio</i> 37: 80-85.
  20. Hauksson, E. 2007. Abundance of grey seals in Icelandic waters, based on trends of pup-counts from aerial surveys. In: T. Haug, M.O. Hammill, and D. Olafsdottir (eds), <i>Grey seals in the North Atalntic and in the Baltic</i>, pp. 85-98. NAMMCO Scientific Publications, Tromso.
  21. Nilssen, K.T. and Haug, T. 2007. Status of grey seals (<i>Halichoerus grypus</i>) in Norway. In: T. Haug, M.O. Hammill, and D. Olafsdottir (eds), <i>Grey seals on the North Atlantic and in the Baltic</i>, pp. 23-31. NAMMCO Scientific Publications, Tromso.
  22. Bowen, W. D., McMillan, J. I. and Blanchard W. 2007. Reduced population growth of gray seals at Sable Island: evidence from pup production and age of primiparity. <i>Marine Mammal Science</i> 23(1): 48–64.
  23. Hiby, L., Lundberg, T., Karlsson, O., Watkins, J., Jüssi, M., Jüssi, I. and Helander, B. 2007. Estimates of the size of the Baltic grey seal population based on photo-identification data. <i>NAMMCO Scientific Publications</i> 6: 163-175.
  24. Mikkelsen, B. 2007. Present knowledge of grey seals (<i>Halicheorus grypus</i>) in Faroese waters. In: T. Haug, M.O. Hammill, and D. Olafsdottir (eds), <i>Grey seals in the North Atlantic and in the Baltic</i>, pp. 79-84. NAMMCO Scientific Publications, Tromso.
  25. Beck, C. A., Iverson, S.J., Bowen, W.D. and Blanchard W. 2007. Sex differences in grey seal diet reflect seasonal variation in foraging behaviour and reproductive expenditure: evidence from quantitative fatty acid signature analysis. <i>Journal of Animal Ecology</i> 76: 490-502.
  26. Harding, K. C., Harkonen, T., Helander, B., Karlsson, O. 2007. Status of grey seals: Population assessment and extinction risk. In: T. Haug, M. O. Hammill & D. Olafsdottir (ed.), <i>.), Grey seals in the North Atlantic and the Baltic </i>, pp. 33-56. NAMMCO Scientific Publications, Tromso.
  27. Bowen, W.D., Iverson, S.J., McMillan J.I. and Boness, D.J. 2006. Reproductive performance in grey seals: age-related improvement and senescence in a capital breeder. <i>Journal of Animal Ecology</i> 75: 1340-1351.
  28. Breed, G.A., Bowen, W.D., McMillan, J.I. and Leonard, M.L. 2006. Sexual segregation of seasonal foraging habitats in a non-migratory marine mammal. <i>Proceedings of the Royal Society B</i> 273: 2319-2326.
  29. Härkönen, T., Dietz, R., Reijnders, P., Teilmann, J., Harding, K., Hall, A., Brasseur, S., Siebert, U., Goodman, S. J., Jepson, P. D., Rasmussen, T. D. and Thompson, P. 2006. A review of the 1988 and 2002 phocine distemper virus epidemics in European harbor seals. <i>Diseases of Aquatic Organisms</i> 68: 115-130.
  30. Lidgard, D.C., Boness, D.J., Bowen, W.D. and McMillan, J.I. 2005. State-dependent male mating tactics in the grey seal: the importance of body size. <i>Behavioral Ecology</i> 16: 541-549.
Évaluateurs & contributeurs (3)Expert
assessor
Bowen, D.
evaluator
Russell, D.J.F. & Bellotto, V.
facilitators
Lowry, L., Ahonen, H., Pollock, C.M., Chiozza, F. & Battistoni, A.

Bowen, D. 2025. Halichoerus grypus (Europe assessment). The IUCN Red List of Threatened Species 2025: e.T9660A231324486. Accessed on 05 May 2026.

Traits biologiques

21 valeurs · 9 sources

Morphologie(5)

Masse adulte
268 kg
AnAge
Masse cerveau
308 g
AnimalTraits
Masse naissance
14 kg
AnAge
Masse au sevrage
41,5 kg
AnAge
Longueur
2,1 m
PanTHERIA

Cycle de vie(1)

Longévité max
43 ans
AnAge
Voir 15 traits de plus (2 catégories)

Reproduction(6)

Sevrage
2,7 sem.
AnAge
Taille de portée
1
AnAge
Maturité sexuelle
5,2 ans
AnAge
Portées par an
1
AnAge
Gestation
7,9 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

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 (10)— redirigent vers cette page

  • Halichoerus griseusNilsson, 1820
  • Halichoerus grypha
  • Phoca atlantica
  • Phoca baltica
  • Phoca griseus
  • Phoca grypusFabricius, 1791
  • Phoca halichoerusThienemann, 1824
  • Phoca macrorhynchus
  • Phoca pachyrhynchus
  • Phocha halichoreus

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