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Phogue du Groenland
Pagophilus groenlandicus(Erxleben, 1777)
Indicateurs du réseau écologique
Comment lire ce graphe
Ce graphe représente les interactions écologiques documentées entre Pagophilus groenlandicus 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
99 partenaires écologiques documentés directement dans GloBI.
Liste rouge IUCN
NT · Quasi menacéecritères A3c↘Décroissante- Évaluation
- 2025 · v3.1
- Altitude
- 0 – m
- Profondeur
- 400 – 0 m
État de la populationTexte officiel évaluation IUCNExpert
The Northwest Atlantic population was assessed in 2023 based on pup production surveys carried out in 2017 (ICES 2023). Pup production was estimated to be 746,500 (95% CI 572,000 - 922,500), which is the lowest since 1994, although not significantly different from the previous survey in 2012 (Stenson et al. 2020). The total Northwest Atlantic population was estimated to be 7.6 million (95% CI 6.6 – 8.8 million) in 2019 (Hammill et al. 2021) and the trend is either stable or increasing slightly (ICES 2023).
A small whelping patch was found near South Greenland in 2007 (Rosing-Asvid 2008), but the source of these animals and the inter-annual stability of this group is not known. However, this finding is particularly interesting in light of climate change.
Menaces identifiées(5 menaces classées CMP-IUCN)
11_1Habitat shifting & alterationRapid DeclinesWhole (>90%)Ongoing11_5Other impactsRapid DeclinesWhole (>90%)Ongoing5_4_2Intentional use: (large scale) [harvest]Rapid DeclinesMajority (50-90%)Past, Unlikely to Return5_4_1Intentional use: (subsistence/small scale) [harvest]Negligible declinesWhole (>90%)Ongoing5_4_4Unintentional effects: (large scale) [harvest]Slow, Significant DeclinesUnknownOngoing
Description complète des menacesTexte détaillé évaluation IUCNExpert
The 20th century saw the advent of steel-hulled ships, and the hunt continued, though Harp Seals became more valued for their pelts than their oil. The size of all three Harp Seal populations has fluctuated through time, driven largely by the size of the commercial harvests (Sergeant 1976). In 1983, the European Economic Community imposed an import ban on seal products, because of public reactions to the white-coat harvest and the average annual commercial harvests fell precipitously. Indigenous groups lobbied the EU parliament successfully and in 2009 exemptions were made for subsistence harvest products. Greenlandic subsistence catches of Harp Seals vastly outnumber commercial harvests in recent decades. Greenland took 50,000-100,00 Harp Seals annually in the 1990s and 2000s (https://nammco.no/catch-database). Harvests in the last decade average some 40,000. Norwegian catches for the West Ice are generally under 10,000 animals per year and little hunting occurs in the White Sea.
Capelin collapses in the Barents Region in the 1980s resulted in Harp Seals shifting their distribution southward and foraging along the coast of Norway, resulting in several major mortality events in shore-based net fisheries. Bycatch mortality from nets was estimated to be 56,647 (perhaps up to 100,000) in 1987, and 21,474 in 1988 though it is thought that actually mortalities might have exceeded 100,000 in each of these years (Haug et al. 1991). These events demonstrated the potential risk that fisheries represent to Harp Seals. A major assessment of fisheries catches vs marine mammal consumption suggests that there is strong potential for direct competition between fisheries and pinnipeds (and other marine mammals) in the Greenland Sea, while competition in the Barents Sea is likely not currently an issue (Skern-Mauritzen et al. 2022).
A major threat to Harp Seals is climate warming (Laidre et al. 2008, 2015, Kovacs et al. 2011, 2012, 2021) which is already impacting all populations through reductions in their drift ice breeding habitats and likely via indirect impacts on their prey populations as well. Recently there have been years with very high pup mortalities because of low ice availability and great variability and generally low survivorship seem to be the new norm (Johnston et al. 2005, Bajzak et al. 2011, Stenson and Hammill 2014, Hammill et al. 2015, 2021, Stenson et al. 2020). In North America, years with high stranding numbers are correlated with environmental conditions, including warm temperatures and little sea ice (Haverkamp et al. 2023). Shifts have occurred in the location of whelping locations in the Greenland Sea and in the Northwest Atlantic during years when ice conditions have been extremely poor (Rosing-Asvid 2008, Stenson et al. 2016, 2020). When pupping occurs outside the traditional areas, the young may be exposed to ice that is less stable and to different prey fields during the period when they are first learning to find food. In the Greenland Sea and in areas off Newfoundland, increased predation from Polar Bears which travel great distances to seek out the pupping concentrations (Peacock et al. 2013) might become a significant survivorship issue. Other changes include shifts in abundance and distribution of many key prey species for Harp Seals which has negatively impacted body condition and reproductive rates in all populations (Øigård et al. 2013, Stenson et al. 2020). Large Atlantic cod stocks in the Northeast Atlantic are likely competing with Harp Seals for prey (Bogstad et al. 2015, Stenson et al. 2020) and the overall borealisation and base-line nutrient shifts in the Barents Sea is likely to continue to negatively impact Harp Seal’s traditional Arctic fish and invertebrate prey populations (Fossheim et al. 2015, de la Vega et al. 2022).
Habitats préférentiels (classification IUCN)
9Marine Neritic★
Mesures de conservation recommandéesStratégies de conservation IUCNExpert
Further research into the population trend of this species is recommended.
Actions de conservation (1)Conservation Actions Classification Scheme — IUCNExpert
1_1Site/area protection
Stress écologiques (10)Stresses Classification — IUCNExpert
1_2Ecosystem degradation1_2Ecosystem degradation2_1Species mortality2_1Species mortality2_1Species mortality2_2Species disturbance2_2Species disturbance2_2Species disturbance2_3_7Reduced reproductive success2_3_8Other
Usage & commerce (1)Use & Trade — IUCNExpert
17Other (free text)internationalnationalsubsistance
Priorités de recherche (1)Research Needed Classification — IUCNExpert
1_2Population size, distribution & trends
Niche IUCN globaleRealms · Systems · LMEs · Growth forms · FAOs — biogéographie IUCNExpert
Royaumes biogéographiques
Systèmes (terrestre/eau douce/marin)
Zones de pêche FAO
Références bibliographiques (30)Sources scientifiques de l'évaluation IUCNExpert
- 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).
- Haverkamp, H., Chang, H.Y., Newcomb, E., Doughty, L., Walk, D., Seton, R., Jones, L.S., Todd, S. and Cammen, K.M. 2023. A retrospective socio-ecological analysis of seal strandings in the Gulf of Maine. <i>Marine Mammal Science</i> 39: 232-250.
- ICES. 2023. Report of the Joint ICES/NAFO/NAMMCO Working Group on Harp and Hooded Seals (WGHARP). <i>ICES Scientific Reports</i> 5(96): 1-75 pp. https://doi.org/10.17895/ices.pub.24306100
- de la Vega, C., Buchanan, P.J., Tagliabue, A., Hopkins, J.E., Jeffreys, R.M., Frie, A.K., Biuw, M., Kershaw, J., Grecian, J., Norman, L., Smout, S., Haug, T. and Mahaffey, C. 2022. Multi-decadal environmental change in the Barents Sea recorded by seal teeth. <i>Global Change Biology</i> 28: 3054-3065.
- Skern-Mauritzen, M., Lindstrøm, U., Biuw, M., Elvarsson, B., Gunnlaugsson, T., Haug, T., Kovacs, K.M., Lydersen, C., McBride, M.M., Mikkelsen, B., Øien N. and Víkingsson, G. 2022. Marine mammal consumption and fisheries removals in the Nordic and Barents seas. <i>ICES Journal of Marine Sciences</i> 79: 1583-1603.
- Hamilton, C.D., Lydersen, C., Aars, J., Biuw, M., Boltunov, A.N., Born, E.W., Dietz, R., Folkow, L.P., Glazov, D.M., Haug, T., Heide-Jørgensen, M.P., Kettemer, L.E., Laidre, K.L., Øien, N., Nordøy, E.S., Rikardsen, A.H., Rosing-Asvid, A., Semenova, V., Shpak, O.V., Svegaard, S., Ugarte, F., Wiig, Ø. and Kovacs, K.M. 2021. Marine mammal hotspots in the Greenland and Barents Seas. <i>Marine Ecology Progress Series </i> 659: 3-28.
- Hammill, M.O., Stenson, G.B., Mosnier, A. and Doniol-Valcroze, T. 2021. Trends in abundance of harp seal, <i>Pagophilus groenlandicus</i>, in the Northwest Atlantic, 1952-2019. DFO Can. Sci. Advis. Sec. Research Document 2021/006.
- Kovacs, K.M., Belikov, S., Boveng, P., Desportes, G., Ferguson, S., Hansen, R., Laidre, K., Stenson, G., Thomas, P., Ugarte, F. and Vongraven, D. 2021. 2021 State of the Arctic Marine Biodiversity Report (SAMBR) Update: 2021. Technical Report. Conservation of Arctic Flora and Fauna International Secretariat. Akureyri, Iceland.
- Stenson, G.B., Haug, T. and Hammill, M.O. 2020. Harp seals: monitors of change in differing ecosystems. <i>Frontiers in Marine Science</i> 7: https://doi.org/10.3389/fmars.2020.569258
- ICES. 2019. ICES/NAFO/NAMMCO Working Group on Harp and Hooded Seals (WGHARP). ICES Scientific Reports 1:72. International Council for the Exploration of the Sea (ICES).
- Enoksen, S., Haug, T., Lindstrøm, U. and Nilssen, K.T. 2017. Recent summer diet of hooded <i>Cystophora cristata</i> and harp <i>Pagophilus groenlandicus</i> seals in the drift ice of the Greenland Sea. <i>Polar Biology</i> 40: 931-937.
- Stenson, G.B., Buren, A.D. and Koen-Alonso, M. 2016. The impact of changing climate and abundance on reproduction in an ice-dependent species, the Northwest Atlantic harp seal, <i>Pagophilus groenlandicus</i>. <i>ICES Journal of Marine Sciences</i> 73: 250-262.
- Hammill, M.O., Stenson, G.B., Doniol-Valcroze, T. and Mosnier, A. 2015. Conservation of Northwest Atlantic harp seals: past success, future uncertainty. <i>Biological Conservation</i> 192: 181-191.
- Carr, S.M., Duggan, A.T., Stenson, G.B. and Marshall, H.D. 2015. Quantitative phylogenomics of within-species mitogenome variation: Monte Carlo and non-parametric analysis of phylogeographic structure among discrete transatlantic breeding areas of harp seals (<i>Pagophilus groenlandicus</i>). <i>PLOS ONE</i> 10(8): https://doi.org/10.1371/journal.pone.0134207
- Bogstad, B., Gjøsæter, H., Haug, T. and Lindstrøm, U. 2015. A review of the battle for food in the Barents Sea: cod vs marine mammals. <i>Frontiers in Ecology and Evolution</i> 3(29): https://doi.org/10.3389/fevo.2015.00029
- Fossheim, M., Primicderio, R., Johannesen, E., Ingvaldsen, R.B., Aschan, M.M. and Dolgov, A.V. 2015. Recent warming leads to a rapid borealization of fish communities in the Arctic. <i>Nature Climate Change</i> doi:10.1038/NCLIMATE2647.
- Laidre, K.L., Stern, H., Kovacs, K.M., Lowry, L., Moore, S.E., Regehr, E.R., Ferguson, S.H., Wiig, Ø., Boveng, P., Angliss, R.P., Born, E.W., Litovka, D., Quakenbush, L., Lydersen, C., Vongraven, D. and Ugarte, F. 2015. Arctic marine mammal population status, sea ice habitat loss, and conservation recommendations for the 21st century. <i>Conservation Biology</i> 29: 724-737.
- Øigård, T.A., Haug, T. and Nilssen, K.T. 2014. From pup production to quotas: current status of harp seals in the Greenland Sea. <i>ICES Journal of Marine Science</i> 71: 537-545.
- Stenson, G.B. and Hammill, M.O. 2014. Can ice breeding seals adapt to habitat loss in a time of climate change? <i>ICES Journal of Marine Science</i> 71: 1977-1986.
- Peacock, E., Taylor, M.K., Laake, J. and Stirling, I. 2013. Population ecology of polar bears in Davis Strait, Canada and Greenland. <i>Journal of Wildlife Management</i> 77: 463-476.
- Øigård, T.A., Lindstrom, U., Haug, T., Nilssen, K.T. and Smout, S. 2013. Functional relationship between harp seal body condition and available prey in the Barents Sea. <i>Marine Ecology Progress Series</i> 484: 287-307.
- Lindstrom, U., Nilssen K.T., Pettersen L.M.S. and Haug, T. 2013. Harp seal foraging behaviour during summer around Svalbard in the northern Barents Sea: diet composition and the selection of prey. <i>Polar Biology</i> 36(305-320).
- Kovacs, K.M., Aguilar, A., Aurioles, D., Burkanov, V., Campagna, C., Gales, N.J., Gelatt, T., Goldsworthy, S.D., Goodman, S.J., Hofmeyr, G.J.G., Härkönen, T., Lowry, L., Lydersen, L., Schipper, J., Sipilä, T., Southwell, C., Thompson, D. and Trillmich, F. 2012. Global threats to pinnipeds. <i>Marine Mammal Science</i> 28: 414-436.
- Berta, A. and Churchill, M. 2011. Pinniped taxonomy: review of currently recognized species and subspecies, and evidence used for their description. <i>Mammal Review</i> 42: 207-234.
- Bajzak, C.E., Hammill, M.O., Stenson, G.B. and Prinseenberg, S. 2011. Drifting away: Implications of changes in ice conditions for a pack-ice breeding phocid, the harp seal (<i>Pagophilus groenlandicus</i>). <i>Canadian Journal of Zoology</i> 89: 1050-1062.
- Kovacs, K.M., Moore, S., Overland, J.E. and Lydersen, C. 2011. Impacts of changing sea-ice conditions on Arctic marine mammals. <i>Marine Biodiversity</i> 41: 181-194.
- Nordøy, E.S., Folkov, L.P., Potelov, V. and Prischemikhin, V. 2008. Seasonal distribution and dive behaviour of harp seals (<i>Pagophilus groenlandicus</i>) of the White Sea- Barents Sea stock. <i>Polar Biology</i> 31: 1119-1135. https://doi.org/10.1007/s00300-008-0453-9
- Rosing-Asvid, A. 2008. A new harp seal whelping ground near South Greenland. <i>Marine Mammal Science</i> 24: 730-736.
- Laidre, K.L., Stirling, I., Lowry, L.F., Wiig, Ø., Heide-Jørgensen, M.P. and Ferguson, S.H. 2008. Quantifying the sensitivity of Arctic marine mammals to climate‐induced habitat change. <i>Ecological Applications</i> 18: 97-125.
- Anon. Fisheries and Oceans Canada (DFO). 2005. <i>Atlantic Seal Hunt 2003 Management Plan, at http://www.dfo-mpo.gc.ca/seal-phoque/reports-rapports/mgtplan-plangest2003/mgtplan-plangest2003_e.htm.</i>.
Évaluateurs & contributeurs (2)Personnes ayant contribué à l'évaluation IUCNExpert
Kovacs, K.M. 2025. Pagophilus groenlandicus (Europe assessment). The IUCN Red List of Threatened Species 2025: e.T41671A212940648. Accessed on 05 May 2026.
Traits biologiques
Morphologie(5)
Cycle de vie(1)
Voir 16 traits de plus (3 catégories)Replier
Reproduction(6)
Écologie & habitat(9)
Divers(1)
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
Note nomenclaturale & synonymesDétails taxonomiques + synonymes CoLExpert
Note nomenclaturale
TAXREF v18 — INPN/MNHNSynonymes (9)— redirigent vers cette page
- Pagophilus groenlandicus groenlandicus(Erxleben, 1777)
- Pagophilus groenlandicus oceanicus(Lepechin, 1778)
- Phoca albicaudaDesmarest, 1822
- Phoca albiniAlessandrini, 1851
- Phoca groenlandicaErxleben, 1777
- Phoca groenlica
- Phoca leucoplaThienemann, 1824
- Phoca oceanicaLepechin, 1778
- Phoca semilunarisBoddaert, 1785
Sources : Catalogue of Life Cross-References (synonymes) · TAXREF v18 INPN/MNHN (commentaires FR).