Hostname: page-component-586b7cd67f-dlnhk Total loading time: 0 Render date: 2024-11-22T04:09:35.183Z Has data issue: false hasContentIssue false

Evidence of distribution overlap between Atlantic and Baltic grey seals

Published online by Cambridge University Press:  15 March 2024

Anders Galatius*
Affiliation:
Section for Marine Mammal Research, Department of Ecoscience, Aarhus University, Aarhus, Denmark
Morten Tange Olsen
Affiliation:
Section for Marine Mammal Research, Department of Ecoscience, Aarhus University, Aarhus, Denmark Section for Molecular Ecology and Evolution, Globe Institute, University of Copenhagen, Copenhagen, Denmark
Marc Allentoft-Larsen
Affiliation:
Section for Marine Mammal Research, Department of Ecoscience, Aarhus University, Aarhus, Denmark
Jeppe Dalgaard Balle
Affiliation:
Section for Marine Mammal Research, Department of Ecoscience, Aarhus University, Aarhus, Denmark
Line Anker Kyhn
Affiliation:
Section for Marine Mammal Research, Department of Ecoscience, Aarhus University, Aarhus, Denmark
Signe Sveegaard
Affiliation:
Section for Marine Mammal Research, Department of Ecoscience, Aarhus University, Aarhus, Denmark
Jonas Teilmann
Affiliation:
Section for Marine Mammal Research, Department of Ecoscience, Aarhus University, Aarhus, Denmark
*
Corresponding author: Anders Galatius; Email: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Grey seals from both the Atlantic and Baltic Sea subspecies are recovering from dramatic declines and recolonising former ranges, potentially leading to overlapping distributions and an emerging subspecies transition zone in Kattegat between Denmark and Sweden. The two subspecies have asynchronous moulting and pupping seasons. We present aerial survey data from 2011 to 2023 in Danish Kattegat during the Atlantic subspecies' moulting (March–April) and pupping (December–January) seasons, as well as the Baltic subspecies' moulting season (May–June). During the Atlantic subspecies' peak moulting season, 82% of the grey seals were recorded north of the island of Læsø (N57°18′, E11°00′). In contrast, during the Baltic moulting season in those years, only 9% of the grey seals were recorded here. This indicates a predominance of Atlantic grey seals in the north and Baltic grey seals in central and southern Kattegat. In 2022 and 2023, three pups were recorded around Læsø during early January, which coincides with the pupping season of northern Wadden Sea grey seals. Previously, pups have been recorded in the same locations during the Baltic pupping season, which demonstrates overlapping breeding ranges. Grey seals are known to have plasticity in the timing of pupping indicated by a west to east cline of progressively later pupping in the eastern North Atlantic. Historical sources document that the Baltic pupping season in Kattegat was earlier than it has been in recent years. Thus, the expanding ranges may be associated with convergence of Atlantic and Baltic subspecies' pupping seasons and potential hybridisation in this emerging transition zone.

Type
Marine Record
Creative Commons
Creative Common License - CCCreative Common License - BYCreative Common License - ND
This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NoDerivatives licence (http://creativecommons.org/licenses/by-nd/4.0), which permits re-use, distribution, and reproduction in any medium, provided that no alterations are made and the original article is properly cited.
Copyright
Copyright © The Author(s), 2024. Published by Cambridge University Press on behalf of Marine Biological Association of the United Kingdom

Introduction

The grey seal (Halichoerus grypus) is a North Atlantic phocid seal, ranging from the northeastern United States and the Canadian Maritimes in the west to the Kola Peninsula of Russia and the Baltic Sea in the east. Two distinct subspecies are currently recognised, one in the North Atlantic Ocean (H. g. atlantica) and one in the Baltic Sea (H. g. grypus), which are characterised by genetic and phenotypic differences (Heptner et al., Reference Heptner, Chapskii, Aren'ev and Sokolov1976; Berta and Churchill, Reference Berta and Churchill2012; Fietz et al., Reference Fietz, Galatius, Teilmann, Dietz, Frie, Klimova, Palsbøll, Jensen, Graves, Hoffman and Olsen2016; Olsen et al., Reference Olsen, Galatius, Biard, Gregersen and Kinze2016), although Galatius et al. (Reference Galatius, Svendsen, Messer, Valtonen, McGowen, Sabin, Dahl, Dahl and Olsen2022) found negligible differences in skull shape. In Europe, the subspecies differences are most apparent in terms of pupping and moulting seasons, which for the Atlantic subspecies in the eastern North Sea region occur from December to January and March to April (Brasseur et al., Reference Brasseur, Patel, Gerrodette, Meesters, Reijnders and Aarts2015; Schop et al., Reference Schop, Aarts, Kirkwood, Cremer and Brasseur2017), while the Baltic subspecies pups and moults in February–March and May–June, respectively (Hook and Johnels, Reference Hook and Johnels1972; Jüssi et al., Reference Jüssi, Härkönen, Helle and Jüssi2008; Galatius et al., Reference Galatius, Ahola, Härkönen, Jüssi, Jüssi, Karlsson and Verevkin2014).

The grey seal was historically abundant along the coasts of continental Europe, but apart from the Norwegian west coast and the Baltic Sea, the species disappeared from the European mainland during the 16th century (Reijnders et al., Reference Reijnders, Vandijk and Kuiper1995; Härkönen et al., Reference Härkönen, Brasseur, Teilmann, Vincent, Dietz, Abt and Reijnders2007). Later, Atlantic grey seals were also hunted to a very low numbers in the United Kingdom, where they were estimated to have an abundance of 500 individuals in 1914 (Lambert, Reference Lambert2002; Lonergan et al., Reference Lonergan, Duck, Thompson, Moss and McConnell2011). This low estimate led to the protection of the species in the United Kingdom, and the population began growing at annual rates of 6–7%, leading to an estimated abundance of 70,000 seals in the 1970s (Summers, Reference Summers1978). In the 1950s, individuals started appearing in the German and Dutch Wadden Sea, and in the 1980s, grey seals were breeding regularly at a few localities here (Scheibel and Weidel, Reference Scheibel and Weidel1988; Reijnders et al., Reference Reijnders, Vandijk and Kuiper1995). Since then, grey seal occurrence and breeding activity has grown at high annual rates in the Wadden Sea area (19% for pup counts in the Netherlands), fuelled by immigration from the United Kingdom (Brasseur et al., Reference Brasseur, Patel, Gerrodette, Meesters, Reijnders and Aarts2015). In 2020, 1921 pups were counted at the peak of the pupping season in the Wadden Sea area and Helgoland, Germany, and during the 2022 moulting season, 8948 grey seals were counted (Schop et al., Reference Schop, Abel, Brasseur, Galatius, Jess, Meise, Meyer, van Neer, Stejskal, Siebert, Teilmann and Thøstesen2022). During this period of growth and recolonisation, the first grey seal pup was recorded in the Danish Wadden Sea in 2014 (Jensen et al., Reference Jensen, Galatius and Teilmann2015). In the Baltic Sea, the Baltic subspecies experienced substantial declines due to 19th and 20th century hunting and 20th century contaminants, yet persisted at a population size in the low thousands (Härkönen et al., Reference Härkönen, Brasseur, Teilmann, Vincent, Dietz, Abt and Reijnders2007), and has since recovered to ca 40,000 animals counted on land during moulting across Sweden, Finland, Estonia, Poland, Germany and Denmark (ICES, 2022).

Kattegat, the sea area between northern Denmark and the west coast of Sweden (Figure 1), is becoming a transition zone between the Baltic and Atlantic grey seals subspecies. In this region, grey seals were abundant during prehistoric times, but became extinct as a breeding stock in the late 19th century as a result of hunting and a bounty campaign (Härkönen et al., Reference Härkönen, Brasseur, Teilmann, Vincent, Dietz, Abt and Reijnders2007; Olsen et al., Reference Olsen, Galatius and Harkonen2018). Fietz et al. (Reference Fietz, Galatius, Teilmann, Dietz, Frie, Klimova, Palsbøll, Jensen, Graves, Hoffman and Olsen2016) used historical mitochondrial DNA analyses to document that the majority of specimens killed in Kattegat during the 19th century bounty hunt were genetically assigned to the Baltic subspecies, while contemporary grey seal hair and tissue samples from Kattegat predominantly were genetically assigned to the Atlantic subspecies. In the 1970s, when systematic surveys of harbour seals were initiated in Kattegat, counts of grey seals in the Danish region were usually in the 20s and restricted to the island of Anholt (Figure 1), and counts remained at this low level until the early 2000s (Härkönen et al., Reference Härkönen, Brasseur, Teilmann, Vincent, Dietz, Abt and Reijnders2007). Recent survey data show that grey seals have increased in abundance in Kattegat and are also present at haul-outs around the islands of Samsø and Læsø (Figure 1), where newborn pups have been recorded during the Baltic grey seal breeding season (Galatius et al., Reference Galatius, Teilmann, Dähne, Ahola, Westphal, Kyhn, Pawliczka, Olsen and Dietz2020).

Figure 1. Map of the study area. The grey seal counts during the Atlantic Ocean (red bars; early April) and Baltic Sea moulting seasons (blue-green bars; late May) for each haul-out in 2022 and 2023 are shown. ND, not determined, count not conducted.

Anecdotally, a couple of observations of breeding attempts have been made, both along the Swedish west coast and in Danish Kattegat (Härkönen et al., Reference Härkönen, Brasseur, Teilmann, Vincent, Dietz, Abt and Reijnders2007), however, to date, there have not been systematic surveys of Kattegat pups or moulting grey seals during the Atlantic grey seal breeding season in late fall and early winter. To address this knowledge gap, monitoring of Danish Kattegat haul-out localities during the Atlantic grey seal breeding and moulting seasons was initiated in December 2021. Here, we use the results of the first two years of this programme, as well as data from the corresponding programme for Baltic grey seals in the region to evaluate occurrence, distribution and pupping activity in the Kattegat transition zone between the two grey seal subspecies.

Materials and methods

The phenology of grey seal pupping and moulting seasons shows some plasticity, in particular in the Atlantic subspecies (Bowen et al., Reference Bowen, den Heyer, Lang, Lidgard and Iverson2020; Bull et al., Reference Bull, Jones, Börger, Franconi, Banga, Lock and Stringell2021; SCOS, 2022). Thus, surveys of the Kattegat were timed to best capture the current Atlantic and the Baltic pupping and moulting seasons, with some input from historical sources (Bynch, Reference Bynch1801) (Figure 2; Supplementary Table 1). We first focus on data from 2022 to 2023, which represent the first two years of aerial surveys of grey seals in Danish Kattegat during the expected Atlantic subspecies pupping (December–January; two surveys per year) and moulting season (March–April; one survey) in the area. These surveys were timed according to data from the Dutch and German Wadden Sea, with pupping observed to mainly occur in mid-December and moulting observed to peak in April (Abt and Koch, Reference Abt and Koch2000; Brasseur et al., Reference Brasseur, Patel, Gerrodette, Meesters, Reijnders and Aarts2015; Schop et al., Reference Schop, Aarts, Kirkwood, Cremer and Brasseur2017, Reference Schop, Abel, Brasseur, Galatius, Jess, Meise, Meyer, van Neer, Stejskal, Siebert, Teilmann and Thøstesen2022). Yet, to also take into account data from the Danish Wadden Sea, where all of the six newborn grey seal pups recorded since 2014 were observed between 28 December and 4 January (Sveegaard et al., Reference Sveegaard, Galatius, Kyhn, Teilmann, Hansen and Høgslund2023), one of the seasonal pupping surveys in Kattegat was conducted in mid-December (to reflect the peak pupping season in the larger Wadden Sea) and one in early January (to reflect pupping in the Danish Wadden Sea). Second, to assess longer time-series trends in Kattegat grey seal abundance, we present data collected in Kattegat since 2011 during the Baltic subspecies moulting (late May–early June) and late pupping seasons (mid-March), the latter period corresponding to the early moulting period of Atlantic grey seals in the Wadden Sea.

Figure 2. Presumed pupping and moulting seasons of Atlantic and Baltic grey seals in the study area. Survey dates for the study are marked with black bars.

Aerial surveys covered all grey seal haul-outs known from historical sources (Bynch, Reference Bynch1801; Faber, Reference Faber1828; Søndergaard et al., Reference Søndergaard, Joensen and Hansen1976), harbour seal monitoring and anecdotal observations in the Danish part of Kattegat, except Bosserne, which was added as a survey site in 2017 after grey seals were recorded here. The haul-outs are named on the Figure 1 map. Surveys were conducted at wind speeds below 10 m s−1 and without precipitation at any locality in the preceding 6 h. All localities were surveyed between 8:00 and 17:00 local time. As tides are negligible in Kattegat, surveys were not timed in relation to these. Two observers both took overlapping photographs using DSLR cameras with 80–200 mm lenses from the same side of the plane of all groups of seals observed through an open window in a single-engine Cessna 172 or 182, flying at 500–600 feet over the haul-out sites. The haul-out at the Knobgrundene sand bank where seals are prone to flushing was overflown at 1000 feet. The digital photographs were subsequently used to count the number of seals present by two independent observers. If the counts for a location differed by more than 5% between the two observers, a third (or more) count(s) was performed until there was agreement between the counts.

Results and discussion

Moulting season

In both 2022 and 2023, the counts of hauled out grey seals in Danish Kattegat during the Atlantic grey seal moulting seasons and those during the Baltic moulting seasons were largely similar, all ranging between 99 and 160 grey seals (Figure 1). However, while the total counts were similar, the geographic distributions of the counts differed between the two seasons; during the Atlantic moulting season, the majority of grey seals were recorded at the Borfeld haul-out north of Læsø Island, while during the Baltic moulting season counts, the majority of grey seals were counted at haul-out sites south of Læsø, including Søndre Rønner skerries and the island of Anholt and Bosserne sand bar.

The observed pattern of partitioning is corroborated by previous counts since 2011 that were conducted during the Baltic pupping season in March and the moulting season in May–June (Figure 3). In the March counts, which overlap with the early Atlantic moulting season, most grey seals were counted north of Læsø, while counts from May to June were dominated by seals in the central and southern areas south of Læsø and around Anholt and Samsø. This indicates that in the Kattegat transition area between the two subspecies, Atlantic grey seals were predominant in the northern part of Kattegat, while Baltic Sea grey seals were most abundant in the central and southern parts. This fits well with the observations by Fietz et al. (Reference Fietz, Galatius, Teilmann, Dietz, Frie, Klimova, Palsbøll, Jensen, Graves, Hoffman and Olsen2016), where most of the contemporary hair and tissue samples collected in Kattegat were from Borfeld at Læsø and genetically assigned to the Atlantic subspecies. Given the lack of contemporary samples from other Kattegat sites, this may have led Fietz et al. (Reference Fietz, Galatius, Teilmann, Dietz, Frie, Klimova, Palsbøll, Jensen, Graves, Hoffman and Olsen2016) to overestimate the relative occurrence of Atlantic grey seals in Kattegat, in light of the monitoring data presented here.

Figure 3. Counts of grey seals in Danish Kattegat during the early Atlantic moulting season in mid-March and the peak Baltic moulting season in late May and early June. Years with no data are not shown. Bars are colour-coded according to season (Atlantic moult: red; Baltic moult: blue-green) and counts in northern Kattegat at Borfeld Reef north of Læsø are in solid colour while counts in southern and central Kattegat at haul-out sites south of Læsø Island and around Samsø, Hesselø and Anholt islands are hatched.

The current moult counts of around 100 grey seals in Kattegat contrasts markedly with the historical dominance of grey seals relative to harbour seals in the region (Søndergaard et al., Reference Søndergaard, Joensen and Hansen1976; Olsen et al., Reference Olsen, Galatius and Harkonen2018) and are dwarfed by contemporary moult counts of harbour seals in August, which have ranged from 8000 to 9000 seals between 2010 and 2021 (Silva et al., Reference Silva, Bottagisio, Harkonen, Galatius, Olsen and Harding2021). This implies that grey seal recolonisation of Kattegat is still in an early stage, yet the survey data presented here indicate that grey seal presence is increasing, particularly in the southern and central parts of Kattegat during the Baltic moulting season (Figure 3). In other areas, e.g. Southeast UK, harbour seal populations have declined when grey seal populations have increased, although no causality linking the contrasting population trajectories has been established (SCOS, 2022). As grey seal and harbour seal diets may overlap in areas where both species occur (Wilson and Hammond, Reference Wilson and Hammond2016; Scharff-Olsen et al., Reference Scharff-Olsen, Galatius, Teilmann, Dietz, Andersen, Jarnit, Kroner, Botnen, Lundström, Møller and Olsen2019), it is likely that there will be direct competition between the species. Furthermore, grey seal predation on harbour seals has been documented since 10 years ago in the North Sea (van Neer et al., Reference van Neer, Jensen and Siebert2015) and recently in the Baltic Sea (Westphal et al., Reference Westphal, Klemens, Reif, van Neer and Dähne2023). Increasing overlap and contact between the two subspecies may facilitate the transmission of this phenomenon.

In the Swedish Kattegat region, seal surveys are not conducted during the grey seal moulting or pupping seasons. However, based on surveys targeting moulting harbour seals in August, grey seals are scarce in this region, averaging between 3 and 17 animals per year along the entire western Swedish coastline in the years 2015–2021 (M. Ahola, Swedish Museum of Natural History, pers. comm.). The corresponding numbers for the Danish part of Kattegat in August range between 23 and 47 grey seals in this period (data not shown).

Pupping season

During our pupping surveys in Kattegat in December–January, we recorded two grey seal pups in the season 2021/2022 (one at Søndre Rønner and the other at Borfeld) and one in 2022/2023 (at Borfeld) around Læsø Island in northern Kattegat (Figure 4). Based on the photos, all three pups were at developmental stage 2 (Jenssen et al., Reference Jenssen, Asmul, Ekker and Vongraven2010), with an estimated age of 4–12 days. This documents the emerging overlap of the breeding ranges of the grey seal subspecies, as there is also breeding activity at these haul-outs during the Baltic grey seal pupping season in late February to mid-March (Galatius et al., Reference Galatius, Teilmann, Dähne, Ahola, Westphal, Kyhn, Pawliczka, Olsen and Dietz2020; Supplementary Table 1). The few observations of pups are concordant with other studies of grey seal recolonisation of their former range, where pupping activity lags behind occurrence during the moulting season and other parts of the year (Brasseur et al., Reference Brasseur, Patel, Gerrodette, Meesters, Reijnders and Aarts2015; Galatius et al., Reference Galatius, Teilmann, Dähne, Ahola, Westphal, Kyhn, Pawliczka, Olsen and Dietz2020; Wood et al., Reference Wood, Murray, Jospehson and Gilbert2020).

Figure 4. Survey photograph of grey seal mother and pup at Borfeld Reef, Kattegat on 6 January 2022. The two animals are highlighted by a white rectangle.

All three grey seal pups in Kattegat were recorded in early January, two on 6 January 2022 and one on 4 January 2023. This is consistent with data from the Danish Wadden Sea, where all six pups detected between 2014 and 2021 were found between 28 December and 4 January (Sveegaard et al., Reference Sveegaard, Galatius, Kyhn, Teilmann, Hansen and Høgslund2023), but late compared to the pupping season in the general Wadden Sea area, which occurs between mid-November and December (Abt and Koch, Reference Abt and Koch2000; Brasseur et al., Reference Brasseur, Patel, Gerrodette, Meesters, Reijnders and Aarts2015). The late parturitions in both the Danish Wadden Sea and Kattegat may be because immigrating breeding females are young, as younger female grey seals are known to pup later than older females (Bowen et al., Reference Bowen, den Heyer, Lang, Lidgard and Iverson2020; Bull et al., Reference Bull, Jones, Börger, Franconi, Banga, Lock and Stringell2021). It has also been observed that pupping may shift earlier as a colony grows (Coulson, Reference Coulson1981). However, the late pupping may also be related to a geographical trend of gradually later pupping times. There is a clockwise sequential cline in pupping date around the UK, with the earliest being Southwest England and Wales, where the pupping season begins in August (Bull et al., Reference Bull, Jones, Börger, Franconi, Banga, Lock and Stringell2021). The cline proceeds from Wales through West Scotland, Shetland, Orkney, East Scotland and finally Southeast England in November–December (SCOS, 2022). Although recent studies cast doubt on the link between sea temperature and the timing of grey seal pupping, at least within local areas (Bowen et al., Reference Bowen, den Heyer, Lang, Lidgard and Iverson2020; Bull et al., Reference Bull, Jones, Börger, Franconi, Banga, Lock and Stringell2021), this pattern is tightly linked with observed mean winter sea surface temperatures from the World Ocean Atlas (Locarnini et al., Reference Locarnini2019).

If the trend of gradually later pupping dates with decreasing winter sea temperature is extrapolated into our study region, it suggests the possibility that the pupping seasons of Atlantic and Baltic grey seal subspecies may start to overlap once the Kattegat transition zone is further colonised from both the warmer North Atlantic and colder Baltic Sea. Indeed, historical sources indicate that Kattegat pupping season fell between the current North Sea and Baltic seasons. For instance, in a detailed contemporary description of the grey seal pup catch for seal oil at Anholt in Kattegat, Bynch (Reference Bynch1801) reported that pups sufficiently fat for capture were killed at Candlemas (2 February). Thus, at this date, many pups must have been near weaning. Based on genetic data, grey seals in Kattegat in the 19th century were of Baltic origin (Fietz et al., Reference Fietz, Galatius, Teilmann, Dietz, Frie, Klimova, Palsbøll, Jensen, Graves, Hoffman and Olsen2016), so this implies a much earlier historic pupping season than currently in the Baltic, where pupping peaks in late February to mid-March.

The Baltic grey seal pupping period in February–March is considered an adaptation to ice breeding. For much of the 20th century, pupping on land in the Baltic was generally not documented (Hook and Johnels, Reference Hook and Johnels1972), however, during this historic period, Baltic grey seals were extinct in areas without ice cover during winter, potentially obscuring a gradient within the Baltic. While it could be rare cases of very late breeding Atlantic grey seal females, our observation of two newborn pups at Borfeld during an opportunistic survey on 26 January 2021 may be an early sign of a phenological adaptation to ice-free circumstances or warmer sea temperatures, potentially bridging the temporal gap between Atlantic and Baltic Sea pupping seasons.

Conclusion and perspectives

There is already genetic evidence of hybridisation between the two subspecies in the western Baltic (Fietz et al., Reference Fietz, Galatius, Teilmann, Dietz, Frie, Klimova, Palsbøll, Jensen, Graves, Hoffman and Olsen2016). The increasing spatial overlap and potential converging moulting and breeding phenology will facilitate further hybridisation between Atlantic and Baltic grey seal subspecies in the transition area in Kattegat. If the breeding seasons of grey seal subspecies converge in Kattegat, current genetic differences may erode over time in this transition area. A continuous range of grey seals in the eastern North Atlantic and Baltic Sea may also increase the potential for pathogen transfer. Also, a decline in the numbers of harbour seals in the recolonised areas may be seen as observed in UK waters (see above). Further knowledge on how Atlantic grey seals use the area, potential relationships to other parts of the range of this subspecies, and possible subspecies hybridisations could be gained by tagging and collecting DNA biopsies from pups born in Kattegat, as well as older seals visiting the area.

Supplementary material

The supplementary material for this article can be found at https://doi.org/10.1017/S0025315424000213

Data availability statement

The data that support this study are available in Supplementary Table 1.

Acknowledgements

We thank Lasse Twiggs Degn, Henrik Egede-Lassen, Siri Elmegaard, Jens Galatius, Emily Griffiths, Mikkel Villum Jensen, Maíra Laeta, Signe May-Andersen, Esteban Iglesias Rivas, Vibe Schourup-Chistensen and Emilie Stepien for their dedicated work as observers on the survey and Ulrich Gosewinkel, Vasili Gramolin and Helmuth Rame for skilful piloting. The survey programmes were funded by the Danish Environmental Protection Agency, Ministry of Environment of Denmark.

Author contributions

A. G. designed the study. A. G., M. A.-L., J. D. B. and L. A. K. led the surveys. A. G. and S. S. analysed the data. A. G., J. T. and M. T. O. interpreted the findings. A. G. wrote the draft article. All authors edited and approved of the final draft.

Financial support

The Danish grey seal monitoring programmes are funded by Danish Environmental Protection Agency.

Competing interest

None.

References

Abt, K and Koch, L (2000) On the pupping season of grey seals (Halichoerus grypus) off Amrum, Northern Germany. Zeitschrift für Säugetierkunde 65, 183186.Google Scholar
Berta, A and Churchill, M (2012) Pinniped taxonomy: review of currently recognized species and subspecies, and evidence used for their description. Mammal Review 42, 207234.CrossRefGoogle Scholar
Bowen, WD, den Heyer, CE, Lang, SLC, Lidgard, D and Iverson, SJ (2020) Exploring causal components of plasticity in grey seal birthdates: effects of intrinsic traits, demography, and climate. Ecology and Evolution 10, 1150711522.CrossRefGoogle ScholarPubMed
Brasseur, SMJM, Patel, TDV, Gerrodette, T, Meesters, EHWG, Reijnders, PJH and Aarts, G (2015) Rapid recovery of Dutch gray seal colonies fueled by immigration. Marine Mammal Science 31, 405426.CrossRefGoogle Scholar
Bull, JC, Jones, OR, Börger, L, Franconi, N, Banga, R, Lock, K and Stringell, TB (2021) Climate causes shifts in grey seal phenology by modifying age structure. Proceedings of the Royal Society B-Biological Sciences 288, 20212284.CrossRefGoogle ScholarPubMed
Bynch, L (1801) Om sælhundefangsten på Anholt. Iris og Hebe 1801, 123.Google Scholar
Coulson, JC (1981) A study of the factors influencing the timing of breeding in the grey seal Halichoerus grypus. Journal of Zoology 194, 553571.CrossRefGoogle Scholar
Faber, F (1828) Kort Efterretning om en zoologisk Rejse til det nordligste Jylland i Sommeren 1827. Tidsskrift for Naturvidenskaberne 4, 110118.Google Scholar
Fietz, K, Galatius, A, Teilmann, J, Dietz, R, Frie, AK, Klimova, A, Palsbøll, PJ, Jensen, LF, Graves, JA, Hoffman, JI and Olsen, MT (2016) Shift of grey seal subspecies boundaries in response to climate, culling and conservation. Molecular Ecology 25, 40974112.CrossRefGoogle ScholarPubMed
Galatius, A, Ahola, M, Härkönen, T, Jüssi, I, Jüssi, M, Karlsson, O, Verevkin, M et al. (2014) Guidelines for seal abundance monitoring in the HELCOM area. HELCOM, 18. Available at http://www.helcom.fi/Documents/Action%20areas/Monitoring%20and%20assessment/Manuals%20and%20Guidelines/Guidelines%20for%20Seal%20Abundance%20Monitoring%20HELCOM%202014.pdfGoogle Scholar
Galatius, A, Svendsen, MS, Messer, D, Valtonen, M, McGowen, M, Sabin, R, Dahl, VA, Dahl, AB and Olsen, MT (2022) Range-wide variation in grey seal (Halichoerus grypus) skull morphology. Zoology 153, 126023.CrossRefGoogle ScholarPubMed
Galatius, A, Teilmann, J, Dähne, M, Ahola, M, Westphal, L, Kyhn, LA, Pawliczka, I, Olsen, MT and Dietz, R (2020) Grey seal Halichoerus grypus recolonisation of the southern Baltic Sea, Danish Straits and Kattegat. Wildlife Biology 2020, wlb.00711.CrossRefGoogle Scholar
Härkönen, T, Brasseur, S, Teilmann, J, Vincent, C, Dietz, R, Abt, K and Reijnders, P (2007) Status of grey seals along mainland Europe form the southwestern Baltic to France. NAMMCO Scientific Publications 6, 5768.CrossRefGoogle Scholar
Heptner, VG, Chapskii, KK, Aren'ev, VA and Sokolov, VE (1976) Mammals of the Soviet Union, Pinnipeds and Toothed Whales: Pinnipedia and Odontoceti, vol II. Moscow: Vysshaya Shkola Publishers.Google Scholar
Hook, O and Johnels, AG (1972) The breeding and distribution of the grey seal (Halichoerus grypus Fab.) in the Baltic Sea, with observations on other seals of the area. Proceedings of the Royal Society Series B-Biological Sciences 182, 3758.Google Scholar
ICES (2022) Working Group on Marine Mammal Ecology. ICES Working Group on Marine Mammal Ecology, 159 p. Available at https://ices-library.figshare.com/articles/report/Working_Group_on_Marine_Mammal_Ecology_WGMME_/20448942Google Scholar
Jensen, LF, Galatius, A and Teilmann, J (2015) First report on a newborn grey seal pup (Halichoerus grypus) in the Danish Wadden Sea since the 16th century. Marine Biodiversity Records 8, e131.CrossRefGoogle Scholar
Jenssen, BM, Asmul, JI, Ekker, M and Vongraven, D (2010) To go for a swim or not? Consequences of neonatal aquatic dispersal behaviour for growth in grey seal pups. Animal Behaviour 80, 667673.CrossRefGoogle Scholar
Jüssi, M, Härkönen, T, Helle, E and Jüssi, I (2008) Decreasing ice coverage will reduce the breeding success of Baltic grey seal (Halichoerus grypus) females. Ambio 37, 8085.CrossRefGoogle ScholarPubMed
Lambert, RA (2002) The grey seal in Britain: a twentieth century history of a nature conservation success. Environment and History 8, 449474.CrossRefGoogle Scholar
Locarnini, RA et al. (2019) World Ocean Atlas 2018, Volume 1: Temperature: National Oceanic and Atmospheric Administration.Google Scholar
Lonergan, M, Duck, CD, Thompson, D, Moss, S and McConnell, B (2011) British grey seal (Halichoerus grypus) abundance in 2008: an assessment based on aerial counts and satellite telemetry. ICES Journal of Marine Science 68, 22012209.CrossRefGoogle Scholar
Olsen, MT, Galatius, A, Biard, V, Gregersen, K and Kinze, CC (2016) The forgotten type specimen of the grey seal [Halichoerus grypus (Fabricius, 1791)] from the island of Amager, Denmark. Zoological Journal of the Linnean Society 178, 713720.CrossRefGoogle Scholar
Olsen, MT, Galatius, A and Harkonen, T (2018) The history and effects of seal-fishery conflicts in Denmark. Marine Ecology Progress Series 595, 233243.CrossRefGoogle Scholar
Reijnders, PJH, Vandijk, J and Kuiper, D (1995) Recolonization of the Dutch Wadden Sea by the grey seal Halichoerus grypus. Biological Conservation 71, 231235.CrossRefGoogle Scholar
Scharff-Olsen, CH, Galatius, A, Teilmann, J, Dietz, R, Andersen, SM, Jarnit, S, Kroner, A-M, Botnen, AM, Lundström, K, Møller, PR and Olsen, MT (2019) Diet of seals in the Baltic Sea region: a synthesis of published and new data from 1968 to 2013. ICES Journal of Marine Science 76, 284297.CrossRefGoogle Scholar
Scheibel, W and Weidel, H (1988) Zum Vorkommen von Kegelrobben (Halichoerus grypus Fabricius, 1791, Phocidae, Pinnipedia) in Schleswig–Holstein. Zoologischer Anzeiger 220, 6570.Google Scholar
Schop, J, Aarts, G, Kirkwood, R, Cremer, JSM and Brasseur, SMJM (2017) Onset and duration of gray seal (Halichoerus grypus) molt in the Wadden Sea, and the role of environmental conditions. Marine Mammal Science 33, 830846.CrossRefGoogle Scholar
Schop, J, Abel, C, Brasseur, S, Galatius, A, Jess, A, Meise, K, Meyer, J, van Neer, A, Stejskal, O, Siebert, U, Teilmann, J and Thøstesen, CB (2022) Grey seal numbers in the Wadden Sea and on Helgoland in 2021–2022. Common Wadden Sea Secretariat, 16. doi: https://www.waddensea-worldheritage.org/sites/default/files/2022_Grey_Seal_Report_0.pdfGoogle Scholar
SCOS (2022) Scientific advice on matters related to the management of seal populations: 2022. University of St Andrews, 206. Available at http://www.smru.st-andrews.ac.uk/files/2023/09/SCOS-2022.pdfGoogle Scholar
Silva, WTAF, Bottagisio, E, Harkonen, T, Galatius, A, Olsen, MT and Harding, KC (2021) Risk for overexploiting a seemingly stable seal population: influence of multiple stressors and hunting. Ecosphere 12, e03343.CrossRefGoogle Scholar
Søndergaard, NO, Joensen, AH and Hansen, EB (1976) Sælernes forekomst og sæljagten i Danmark. Dansk Vildtundersøgelser 26, 180.Google Scholar
Summers, CF (1978) Trends in the size of British grey seal populations. Journal of Applied Ecology 15, 395400.CrossRefGoogle Scholar
Sveegaard, S, Galatius, A, Kyhn, L and Teilmann, J (2023) Havpattedyr – sæler og marsvin. In Hansen, JW and Høgslund, S (eds), Marine Områder 2021. Aarhus: Aarhus Universitet – DCE – Nationalt Center for Miljø og Energi, pp. 119135.Google Scholar
van Neer, A, Jensen, LF and Siebert, U (2015) Grey seal (Halichoerus grypus) predation on harbour seals (Phoca vitulina) on the island of Helgoland, Germany. Journal of Sea Research 97, 14.CrossRefGoogle Scholar
Westphal, L, Klemens, L, Reif, F, van Neer, A and Dähne, M (2023) First evidence of grey seal predation on marine mammals in the German Baltic Sea. Journal of Sea Research 192, 102350.CrossRefGoogle Scholar
Wilson, LJ and Hammond, PS (2016) Comparing the diet of harbour and grey seals in Scotland and eastern England. Marine Scotland 35, 130. doi: https://data.marine.gov.scot/sites/default/files/SMFS%20Vol%207%20No%2019.pdfGoogle Scholar
Wood, SA, Murray, KT, Jospehson, E and Gilbert, J (2020) Rates of increase in gray seal (Halichoerus grypus atlantica) pupping at recolonized sites in the United States, 1988–2019. Journal of Mammalogy 101, 121128.CrossRefGoogle ScholarPubMed
Figure 0

Figure 1. Map of the study area. The grey seal counts during the Atlantic Ocean (red bars; early April) and Baltic Sea moulting seasons (blue-green bars; late May) for each haul-out in 2022 and 2023 are shown. ND, not determined, count not conducted.

Figure 1

Figure 2. Presumed pupping and moulting seasons of Atlantic and Baltic grey seals in the study area. Survey dates for the study are marked with black bars.

Figure 2

Figure 3. Counts of grey seals in Danish Kattegat during the early Atlantic moulting season in mid-March and the peak Baltic moulting season in late May and early June. Years with no data are not shown. Bars are colour-coded according to season (Atlantic moult: red; Baltic moult: blue-green) and counts in northern Kattegat at Borfeld Reef north of Læsø are in solid colour while counts in southern and central Kattegat at haul-out sites south of Læsø Island and around Samsø, Hesselø and Anholt islands are hatched.

Figure 3

Figure 4. Survey photograph of grey seal mother and pup at Borfeld Reef, Kattegat on 6 January 2022. The two animals are highlighted by a white rectangle.

Supplementary material: File

Galatius et al. supplementary material

Galatius et al. supplementary material
Download Galatius et al. supplementary material(File)
File 28.9 KB