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Occurrence, distribution and behaviour of beluga (Delphinapterus leucas) and bowhead (Balaena mysticetus) whales at the Franklin Bay ice edge in June 2008.

ABSTRACT. Ice edges and polynyas have long been noted for their high biological productivity within the Arctic environment. In June 2008, an aggregation of belugas and bowheads was identified at the Franklin Bay ice edge in the eastern Beaufort Sea, adjacent to the Cape Bathurst polynya. We conducted five ice-edge surveys by helicopter to study the distribution and behaviour of the whales. Bowheads were sighted in significantly shallower water than belugas. In addition, we used the helicopter platform to observe behaviour. Belugas and bowheads were engaged in directed travel and diving near and under the ice. Five beluga dives were timed and found to have an average duration of 106 [+ or -] 61 s ([+ or -] SD) and a range of 30-197 s. One bowhead under-ice dive was timed and had a duration of 417 s. The under-ice dives are consistent with feeding behaviour observed for belugas and bowheads in other ice-edge locations. We hypothesize that higher prey densities along the Franklin Bay ice edge than in the adjacent open water may attract belugas and bowheads to the ice edge in June. Further research is needed to identify the abundance and type of prey species consumed and to assess the relative energetic importance of spring ice-edge feeding to the eastern Beaufort Sea beluga and bowhead populations.

Key words: aerial survey, polynyas, floe edge, Delphinapterus leucas, Balaena mysticetus, diving behaviour, habitat selection, fast ice

RESUME. Depuis longtemps, les lisieres de glace et les polynies sont connues pour leur grande productivity biologique au sein de l'environnement arctique. En juin 2008, un groupement de belugas et de baleines bottles a ete repere a la lisiere de glace de la baie Franklin, dans l'est de la mer de Beaufort, lisiere adjacente a la polynie du cap Bathurst. Au moyen d'helicopteres, nous avons effectue cinq etudes de lisieres de glace afin d'examiner la repartition des baleines de meme que leur comportement. Les baleines bottles evoluaient dans des eaux beaucoup moins profondes que les belugas. De plus, nous avons etudie le comportement des baleines a partir de la plateforme destinee aux helicopteres. Les belugas et les baleines bottles se deplacient de maniere dirigee et plongeaient pres de la glace et sous celle-ci. Les plongeons de belugas ont ete chronometres, et leur duree moyenne s; etablissait a 106 [+ or -] 61 s ([+ or -] SD), avec une &endue de 30-197 s. Le plongeon sous glace d'une baleine bottle a dure 417 s. Les plongeons sous glace vont de pair avec le comportement alimentaire observe chez les belugas et les baleines bottles d'autres emplacements en lisieres de glace. Nous avancons l'hypothese que la plus grande densite de proies le long de la lisiere de glace de la baie Franklin comparativement aux eaux libres adjacentes peut attirer les belugas et les baleines bottles a la lisiere de glace en juin. Il faut pousser les recherches plus loin pour determiner l'abondance et le type d'especesproles consommees et pour evaluer l'importance energetique relative de l'alimentation a la lisiere de glace au printemps pour les populations de belugas et de baleines bottles de Pest de la mer de Beaufort.

Mots cles: etude aerienne, polynies, glace de banc, Delphinapterus leucas, Balaena mysticetus, comportement de plongee, selection de l'habitat, glace rapide

Traduit pour la revue Arctic par Nicole Giguere.

INTRODUCTION

Arctic animals have evolved and adapted to survive large seasonal variations in temperature, light, and sea-ice extent by feeding opportunistically within ephemeral areas offering a high density of food items. As in other zones with extreme climates, such as deserts and alpine zones, certain areas have relatively low faunal and floral densities, while others serve as oases with much higher species abundance. Within the Arctic marine environment, polynyas and ice edges have long been recognized as habitats with higher species abundance than the surrounding ice-covered regions (Stirling, 1980, 1997; Dunbar, 1981). Ice edges also contribute to primary productivity in the Arctic and may be more productive than the open-water environment at high latitudes (Perrette et al., 2011). From marine mammals to birds and plankton, these areas of open water adjacent to ice-covered waters support a large variety of life, especially in spring, when migrating animals return to high latitudes (Stirling, 1997).

Beluga (Delphinapterus leucas) and bowhead (Balaena mysticetus) whales are two of the Arctic marine mammals that are often reported along ice edges and in polynyas (Fay, 1974; Carroll and Smithhisler, 1980; Stirling, 1980; Reeves et al., 1983; Carroll et al., 1987; Crawford and Jorgenson, 1990; Cosens and Dueck, 1991; Richard et al., 1998; Stewart, 2001; Harwood and Smith, 2002). Beluga behaviour at fast-ice edges is affected by the location of the edge in relation to the migration route whether or not the ice is blocking the whales' travel) and includes directed movement (Bradstreet, 1982; Cosens and Dueck, 1991; Huntington et al., 1999), back-and-forth movement (Bradstreet, 1982), circling (Cosens and Dueck, 1991), diving under the ice (Bradstreet, 1982), and under-ice feeding (Huntington ct al.. 1999). Bowhcad whales also engage in under-ice feeding, at least during spring migration (Carroll et al., 1987).

Within the Arctic, belugas and bowheads follow yearly migration patterns that largely coincide with sea-ice conditions (DR), 2002; Ainley et al., 2003). They migrate into seasonally ice-covered regions in spring, following breakup, and migrate out in fall, prior to freeze-up. The Eastern Beaufort Sea (EBS) populations of bowheads and belugas overwinter in the Bering Sea (Fraker, 1979). The timing and direction of the spring migration of both whales are influenced by ice conditions (Fraker, 1979; Carroll and Smithhisler, 1980; Moore and Reeves, 1993; Huntington et al., 1999; Mymrin et al., 1999; Quakenbush and Huntington, 2010). In the past, bowheads and belugas traveled through the waters of northwestern Alaska in late April and early May (Fraker, 1979; Quakenbush and Huntington, 2010), but more recently, bowheads have been seen as early as late March and early April (Quakenbush and Huntington, 2010). Traveling through leads far offshore, bowheads reach the PBS in early to mid May (Braham et al., 1980), while belugas arrive in mid to late May (Fraker, 1979). The first destination for both groups is the Cape Bathurst polynya and flaw lead system in Amundsen Gulf (Fraker, 1979). This region is also used throughout the summer (Stirling, 1980). Belugas are believed to feed for four to six weeks in Amundsen Gulf (Fraker, 1979; Stirling, 1980) before part of the population migrates west to the Mackenzie estuary (Fraker, 1979; Richard et al., 2001). Similarly, bowheads also Occupy the area near Cape Bathurst earlier in the year than they occupy the Mackenzie Delta region (Fraker and Bockstoce, 1980). The Cape Bathurst polynya is believed to be an important feeding ground for both belugas and bow-heads in the spring (Stirling, 1980).

In 2007 and 2008, the EBS was the target of extensive scientific research during the international Polar Year (IPY) Circumpolar Flaw Lead (CFL) System Study (Barber et al., 2010). As part of the GT study, ice-edge use by belugas and bowheads was investigated from the CCGS Amundsen research icebreaker and by aerial surveys. Focusing our investigation on Franklin Bay, we documented the occurrence, diving behaviour, and habitat use of an aggregation of belugas and bowheads at the Franklin Bay fast-ice edge in June 2008.

MATERIALS AND METHODS

Study Area

The study area is in Franklin Bay, Northwest Territories, Canada. This bay is situated in the southeastern Beaufort Sea, on the east side of Cape Bathurst (Fig. 1). Oceanic water masses in the Beaufort Sea include a surface layer of Pacific origin (Polar-Mixed Layer) (McLaughlin et al., 1996) that circulates anticyclonically (Coachman and Aagaard, 1974) and a region below the top 40 to 60 ill, known as the Beaufort undercurrent (Pacific Halocline), where circulation is cyclonic, or reversed (Aagaard et al., 1989). Waters of Atlantic origin are found between 200 and 600 m (Atlantic Layer) (McLaughlin et al., 1996). In Amundsen Gull in 2008, the depth ranges of these three water masses were measured by Geoffroy et al. (2011), who report the presence of the Polar-Mixed Layer from 0 to 60 m, the Pacific Halocline from 60 to 200 m, and the Atlantic layer from ~200 m to the bottom. Franklin Bay reaches maximum depths of 220 m, and a major river, the Horton River, drains into its west side (Fig. 1). On average in Franklin Bay, freeze-up begins in September, while breakup starts in late June or early July (Galley et al., 2008), but in the spring of 2008, sea-ice concentrations and extent were relatively low throughout the eastern Beaufort Sea (Fig. 2). A fast-ice edge was present in the bay until 21 June 2008, extending to the mouth of the Horton River. On 21 June, large fractures formed in the ice, and by 22 June, those fractures widened to the point where there was considerable open water in the bay (Fig. 3).

Aerial Surveys

A helicopter (Messerschmidt BO 105) was used to conduct aerial surveys and to record beluga and bowhead behaviour at the Franklin Bay fast-ice edge. Ice-edge surveys were conducted on 11, 15, 16, 18, and 21 June 2008 (Fig. 3). On 24 June, a final survey was flown through the area after the fast ice had broken up (Fig. 3). In all cases, the helicopter flew along the fast-ice edge from west to east at an altitude of 305 in (1000 ft) and a speed of 185 km/ hr. The position of the helicopter was logged every 2 s on a Global Positioning System (GPS) unit. An experienced whale observer (NA) sat in the front left seat and counted all groups of belugas and bowheads and the number of individuals in each group. For the purpose of our research, a group was defined as individuals in relatively close proximity (within 1 body length for belugas and 5 body lengths for bowheads) and behaving cohesively. Direction of travel of the groups was also noted when possible. When sightings were numerous, the helicopter slowed down to allow for complete counts of visible animals before continuing along the ice edge.

Two additional flights were conducted on 15 and 21 June to study behaviour at the floe edge. During these flights, the helicopter flew at an altitude of 305 m along the fast-ice edge until a group of animals was encountered. The aircraft then slowed or hovered, and a Sony HDR-HC3 handheld video camera was used to film activity. Whales were monitored for responses to the presence of the helicopter. Following Patenaude et al. (2002), a disturbance response was defined as unusual behaviour, such as vigorous swimming, abrupt dives, tail slapping, or animals orienting away from the aircraft.

Data Proessing

From the GPS log track, we geo-referenced sightings by using the location of the helicopter as an approximation of the location of the sightings. The videos from the behavioural flights were viewed to time complete dives and surface intervals (i.e., time spent at the surface between dives). Complete dives were timed when we could be reasonably certain from the group size and location that the same animals were being observed before and after a dive. The start and end of a dive were determined by the first animal of a group diving or surfacing. Surfacing times for groups were calculated in the same way. When possible, dives were classified as shallow or deep on the basis of the angle of descent of the animals (Fig. 4). For shallow dives, whales dove beneath the ice edge while almost parallel with the surface. During deep dives, whales descended at a steep angle (approaching 90') from the surface to depth.

GIS Methods and Analytical Methods

Using ArcGIS 9.2, locations of beluga and bowhead sightings were overlaid on a bathymetric raster layer of the region and a vector layer of the Northwest Territories (Geogratis http://geogratis.cgdi.gc.ca/). The bathymetric layer was generated from the International Bathymetric Chart of the Arctic Ocean (Jakobsson et al., 2008). We calculated the seafloor slope in ArcGIS 9.2 from the IBCAO dataset, using a pixel size of 2 km x 2 km.

Kruskal-Wallis one-way analysis of variance was run in Systat 11 to test whether beluga and bowhead locations differed with respect to depth, seafloor slope, and distance to the mouth of the Horton River. We used ArcGIS 9.2 to determine the values of these three environmental descriptors at each sighting location. Water depth and seafloor slope were used as explanatory variables because these two factors have been found to correlate with the distribution of belugas in the eastern Beaufort Sea in June (Asselin et al., 2011). The choice of distance to the mouth of the Horton River as a third explanatory variable was based on knowledge that belugas enter estuaries in large numbers after breakup in late-spring/early-summer (Norton and Harwood, 1985; Frost and Lowry, 1990; Harwood et al., 1996; Martin et al., 2001; Hobbs et al., 2005). In order to provide measurements of the "available habitat" within our ice-edge study area, the fast-ice edge on 16 June was used as the general location of the edge during whale observations (11--21 June). In ArcGIS 9.2, the depth, seafloor slope, and distance to the mouth of the Horton River were determined for 799 points at 100 m intervals along this fast-ice edge.

RESULTS AND DISCUSSION

During the five surveys along the Franklin Bay fast-ice edge, we sighted a total of 192 belugas and 15 bowheads (Table 1). Juveniles of both species were also present, including at least one neonate beluga sighted on 15 June. The number of groups sighted in a single survey ranged from 1 (on 16 June) to 58 (11 June) for belugas, and from 1 (15 and 18 June) to 5 (11 June) for bowheads (Table 1, Fig. 3). On 24 June, after breakup of the fast ice, no belugas or bowheads were observed along the survey route across the bay (Fig. 3).

TABLE 1. Summary of survey observations from helicopter surveys along
the Franklin Bay ice edge, 11 June to 24 June 2008.

                    Beluga                 Bowhead

Date     Survey  Number of        Total  Number of        Total
         length     groups  individuals     groups  individuals
           (km)

11 June      85         58          100          5            5

15 June      88         16           24          1            1

16 June      80          1            1          4            6

18 June      87          4            4          1            1

21 June      75         44           63          2            2

24 June     133          0            0          0            0

Totals      548        123          192         13           15


Behaviour at the Fast-Ice Edge

Generally, belugas and bowheads were engaged in traveling or diving behaviour. Not many animals were observed resting at the surface. Much of the traveling was parallel to the ice edge, in a westerly or easterly direction, although some individuals were observed swimming towards or away from the ice edge. A response to the helicopter was noted once, when a beluga immediately dove as the shadow of the helicopter passed over it. Both shallow and deep dives (as determined by body angle) were observed for belugas traveling and for belugas diving near or under the ice. On 15 June, of 18 beluga dives that were classified for depth, 10 were shallow and 8 were deep. Bowheads were observed resting at the surface, traveling, and diving. The orientation of the whales was noted for 66 groups of belugas and 8 groups of bowheads. During these sightings, belugas were oriented west (n = 40, 60.6%), east (n = 13, 19.7%), towards the ice (n = 9, 13.6%) and away from the ice (n = 4, 6.1%). Bowheads were oriented west (n = 3, 37.5%), towards the ice (n = 4, 50.0%) and away from the ice (n = 1, 12.5%).

On 15 June, 25 belugas were observed and videotaped during a 20-minute period. The results presented are for dive durations and surface intervals of groups. Group size was found to be dynamic, ranging from one to five individuals as animals joined and left groups, While some belugas swam along the edge in an easterly or westerly heading, others were observed first swimming along the ice edge and then turning suddenly and diving under the ice. We were able to time five under-ice dives, and they had an average duration of 106 [+ or -] 61 s (SD) and a range of 30-197 s. Four surface intervals were also timed and found to have an average duration of 52 [+ or -] 24 s (SD) and a range of 23-77 s. On 21 June, one bowhead under-ice dive was timed and had a duration of 417 s (0:06:31).

While average dive and surface-interval duration can provide information on general beluga activity, the detailed activities of individuals or beluga groups can help elucidate the potential role of the ice edge. Two examples of behaviour observed on 15 June follow.

Example 1: One beluga, observed for 130 s, came out from under the ice as it surfaced from depth. After a 23 s surface interval, it executed a 30 s deep dive in the same region as its initial surfacing. The beluga then spent 77 s at the surface and swam back and forth along the ice edge prior to diving once again at the same location.

Example 2: A group of three belugas, observed for 452 s, was first seen swimming along the ice edge heading east. They then turned and dove under the ice edge in succession. They emerged from the ice 121 s later with a fourth individual. The group of four belugas then spent 43 s at the surface swimming along the ice edge and doing small dives before diving under the edge, at a shallow angle and once again in succession. After 197 s, the group of four belugas re-emerged (Fig. 5.1) with a fifth whale close behind (Fig. 5.2). The group of four then appeared to chase the fifth beluga (Fig. 5.3). After 64 s at the surface, the group of four dove under the ice edge once again at a shallow angle while the fifth whale dove deeper (Fig. 5.4, 5.5, and 5.6).

Belugas diving under fast ice have also been reported in the spring in Norton Bay, Alaska, where belugas feed first on herring and later on tomcod under the ice (Huntington et al., 1999). Mymrin et al. (1999) indicate that when belugas are feeding at the ice edge in the northern Bering Sea, they dive under the ice as a group and resurface to breathe in the same place, but when migrating, in contrast, they swim in one direction and move rapidly out of sight (Mymrin et al., 1999). The similarity of the behaviours described by Huntington et al. (1999) and Mymrin et al. (1999) to those we observed in Franklin Bay in June 2008 suggest that the belugas we observed were feeding under the ice.

Belugas forage on a large variety of fish species and invertebrates (Kleinenberg et al., 1964; Seaman et al., 1982), but arctic cod (Boreogadus saida) has been identified as their main prey throughout the Arctic (Kleinenberg et al., 1964; Heide-Jorgensen and Teilmann, 1994; Dahl et al., 2000; Loseto et al., 2009). Arctic cod are considered ice-associated and have been observed beneath sea ice, as well as within its cracks and crevices (Bradstreet, 1982; Percy et al., 1985; Lonne and Gulliksen, 1989; Crawford and Jorgenson, 1990, 1993; Gradinger and Bluhm, 2004). They have also been found at depth in Admiralty Inlet (Crawford and Jorgenson, 1990)--and, notably, in Franklin Bay--in March and April (Benoit et al., 2008). In the winter of 2008, Geoffroy et al. (2011) identified large aggregations of arctic cod in Amundsen Gulf These were found until breakup in the last week of April and solely in ice-covered waters * at depths greater than 221 m (Geoffroy et al., 2011), which exceeds the depth of Franklin Bay. Craig et al. (1982) indicate that arctic cod are not numerous in near-shore habitats during the start of the open-water season, and scuba divers (H. Hop, pers. comm. 2010) and fish researchers involved in the CFL system study did not identify any significant aggregations of adult arctic cod in Franklin Bay in June 2008. It is possible that belugas at the Franklin Bay ice edge were under-ice feeding (for shallow dives) and benthic foraging (for deep dives) on arctic cod, but we hypothesize that other prey items may explain the attraction of the floe edge at that time.

In coastal waters of western Alaska in summer, belugas consume saffron cod (Eleginus gracilis), sculpins (Family Cottidae), and various salmon species (Seaman et al., 1982), while in the Mackenzie River estuary, they consume arctic cisco (Coregonus autumnalis), burbot (Low iota), and whitefish (Coregonus spp.) (Harwood and Smith, 2002). In Norton Bay, Alaska, in spring, belugas feed under the ice on Pacific herring (Clupea pallasi) and tomcod (Eleginus gracilis) (Huntington et al., 1999). The Horton River does have a small population of arctic char (Salvelinus alpinus) (MacDonell, 1989) that moves seaward in spring (McCart, 1980) and may have been targeted by belugas. However, Pacific herring is the main fish caught in Franklin Bay (Percy et al., 1985), and these fish are known to aggregate for spawning in subtidal waters in spring (Hay, 1985). We consequently hypothesize that Pacific herring may have been one of the prey items targeted by belugas in Franklin Bay in June 2008.

The behaviour of the group of four belugas in example 2 (above and Fig. 5) first resembled feeding behaviour, as described by Mymrin et al. (1999). These four whales also displayed aggressive behaviour towards the fifth whale, which matches the description of a chase and possibly a charge given in the beluga ethogram (developed with belugas in captivity) in DiPaola et al. (2007). In other odontocetes, instances of aggression are often related to male-male competition (Norris, 1967; MacLeod, 1998; Scott et al., 2005). Loseto et al. (2006) hypothesized that smaller male belugas in the EBS in summer may be segregating from large males partly to avoid aggression. Without knowing the sex of the animals, we cannot interpret whether the interaction we observed was intra-sexual competition.

Bowheads were also observed diving repeatedly under the ice and swimming along and very close to the fast-ice edge. In Alaska, bowheads have been observed diving below the fast ice to feed (Carroll et al., 1987; Quakenbush and Huntington, 2010) and also skim-feeding by swimming along fast-ice edges with their mouths open (Quakenbush and Huntington, 2010). An examination of prey items from bowheads feeding under the ice near Point Barrow, Alaska, determined that the whales were mainly feeding pelagically. on copepods and euphausiids, but some near-bottom feeding was also identified (Carroll et al., 1987). Similarly, euphausiids and copepods are the main prey of bowheads in the Alaskan Beaufort Sea in spring (Lowry et al., 2004). In summer, bowheads in the Beaufort Sea engage in three types of feeding: skim-feeding at or near the surface, in the water column, and at or near the bottom (Wursig et al., 1989), and stomach contents from one whale taken in August in the Mackenzie Delta contained mainly pelagic prey (Pomerleau et al., 2010). Notably, copepods make up 90% of bowhead prey biomass in the Canadian Beaufort Sea (Schell and Saupe, 1993), and two copepods, Calanus hyperboreus and C. glacialis, are present in Franklin Bay in winter (Benoit et al., 2008). In Franklin Bay in May and June 2008, the three copepods C. glacialis, Metridia Tonga, and C. hyperboreus dominated the large class of zooplankton (> 1000 p.m), with C. hyperboreus contributing the most to biomass (G: Darnis, unpubl. data). Furthermore, from 8 to 21 June 2008 in Franklin Bay, at sampling depths of 0 to 5 m, the highest concentrations of copepods were found within 1 m of the ice undersurface, and C. glacialis was the most abundant (Hop et al., 2011). From these findings, we conclude that bowheads observed diving under the ice in Franklin Bay were likely engaged in pelagic feeding on copepods. Those observed swimming along the ice edge were either skim-feeding, also on copepods, or traveling.

Differences in the Distribution of Beluga and Bowhead

The distribution of water depths of beluga sightings differed significantly from that of bowhead sightings (KW = 5.034, df = 1, p = 0.025), with belugas on average in deeper water (Fig. 6). On average, belugas were closer than bowheads to the mouth of the Horton River but this difference was not significant (KW = 2.835, df = 1,p = 0.092) (Fig. 6). Also, beluga and bowhead sighting locations did not differ significantly with respect to seafloor slope (KW = 1.181, dr = 1,p = 0.277) (Fig. 6).

In the Alaskan Arctic, in summer and fall, belugas were also found to use deeper waters than bowheads, reflecting the differences in their feeding modes and prey items (Moore and DeMaster, 1998). Differences in the feeding ecology of belugas and bowheads, while on a much smaller scale, may also explain the difference in distributions with respect to water depth along the Franklin Bay ice edge in June 2008. While bowheads consume fairly specific prey types, eating mainly copepods and euphausiids (Lowry et al., 2004), belugas are able to exploit a variety of prey species (Kleinenberg et al., 1964; Seaman et al., 1982). Consequently, while the range of depth distributions is similar for belugas and bowheads, the 50th percentile of those values is narrower for bowheads than it is for belugas (Fig. 6). Although consideration must be given to the possible influence of the smaller sample size for bowheads, the distribution may indicate that belugas are foraging on a variety of prey distributed at various depths, while bowheads are restricted to a few species associated with a narrower depth range. Similarly, while not statistically significant, the relative proximity of belugas to the Horton River may indicate they are also exploiting nearshore or riverine resources. The lack of difference in the seafloor slope distribution between bowhead and beluga sightings may indicate that this variable does not vary sufficiently in Franklin Bay to measure a significant difference, that belugas and bowhead relate to seafloor slope similarly, or that we did not have a sufficiently large sample size to identify a difference.

The importance of these observations must be assessed cautiously, as the data were not collected through systematic surveys as required to compare ice-edge regions to offshore regions. Also, our survey design did not provide information on both habitat available and habitat used, and therefore conclusions on selection must be considered cautiously. Thus, further research is needed to understand foraging behaviour of belugas and bowheads at the Franklin Bay ice edge. A larger sample size, especially for bowhead whales, would help us to understand the differences in habitat selection for these two species. While a response to the helicopter was noted only once, it is possible that the helicopter affected the behaviour of belugas and bowheads in ways too subtle for us to notice. Large-scale, systematic surveys could help us to understand the importance of fast-ice edges to belugas and bowheads and to determine. the overall spring distributions of both species within the EBS.

The present study is the first description of beluga and bowhead activity at a fast-ice edge in the EBS. Belugas are known to aggregate at ice edges to await breakup (Cosens and Dueck, 1991; Stewart, 2001); however, as the Franklin Bay ice edge does not block their migration path, which is generally east-west (DFO, 2000), we hypothesize that this floe-edge habitat might have been a preferred habitat compared to the surrounding open-water areas. The presence of both belugas and bowheads at the Franklin Bay ice edge, along with the probable feeding behaviour identified, underlines the importance of ice edges and polynyas to Arctic marine mammals noted by others (Stirling, 1980, 1997; Dunbar, 1981). Dunbar (1981) emphasized that it was the ice edge, as opposed to the open water, that appeared to be key to the biological importance of polynyas. In spring in the Arctic, ice-edge phytoplankton blooms can be observed within 20 days of ice retreat (Perrette et al., 2011), and upwelling along ice edges can further increase primary productivity (Mundy et al., 2009). These increases in primary productivity can lead to increases in productivity at higher trophic levels that benefit foraging cetaceans (Croll et al., 2005). For cetaceans in the Arctic, which rely on dense aggregations of prey (Moore and DeMaster, 1998), habitat selection is likely linked to foraging success. We consequently hypothesize that the Franklin Bay fast-ice edge may provide bowheads with the higher-than-average concentrations of zooplankton required to meet their energetic needs (Lowry, 1993) and belugas with one or many of the fish prey species on which they forage.

Laidre et al. (2008) considered Arctic cetaceans to be more resilient to climate change than other Arctic marine mammals, partly because they are less sensitive to sea-ice changes. While Asselin et al. (2011) found that EBS belugas preferred heavy ice cover and water depths of 200-500 m in spring, the present results confirm that belugas can also exploit fast-ice edges. These 2008 observations lend evidence to the hypothesis proposed by Asselin et al. (2011) that EBS belugas may shift their distribution shoreward and to fast-ice edges in spring during years with low ice concentrations. Belugas in West Greenland shift their distribution in response to changes in sea-ice extent (Heide-Jorgensen et al., 2010), while bowheads have been found to have improved body condition during low-ice years, which may be due to increased primary productivity (George et al., 2009). Belugas in the EBS may adapt to a loss of sea ice by concentrating their foraging effort in areas with dependable concentrations of prey, such as ice edges, while bowheads may thrive in an environment with less sea-ice extent. However, because of the springtime coupling of sea-ice extent and phytoplankton (Heide-Jorgensen et al., 2007), it is likely that the spring feeding habitat of bowheads will be altered by climate change.

The identification of an aggregation of belugas and bowheads at the Franklin Bay ice edge indicates that this habitat is important to whales in the EBS in the spring. The respective distributions of belugas and bowheads differed significantly in terms of water depth, with belugas being on average in deeper water. While belugas and bowheads were observed traveling along the ice edge, both species also engaged in repeated dives under the ice. These dives are consistent with feeding behaviour observed in other locations and provide further evidence of the biological importance of ice edges and polynyas to marine mammals. While we could not conclusively identify prey species with the data available, we hypothesize that belugas and bow-heads may find higher-than-average concentrations of prey at the Franklin Bay ice edge in the form of a variety of fish species (for belugas) and abundant zooplankton (for bowheads). Further research is needed to fully examine the distribution of belugas and bowheads in spring in the EBS and to investigate the prey species being targeted by foraging dives.

ACKNOWLEDGEMENTS

We gratefully acknowledge the assistance in the field of the officers and crew of the CCGS Amundsen and particularly of the helicopter pilots, Guillaume Carpentier and Serge Arsenault. Klaus flochheim also provided field support and the photos used in Figures 4 and 5. This work was supported by the Natural Sciences and Engineering Research Council of Canada, the Canada Research Chairs program, the Department of Fisheries and Oceans, and ArcticNet. This is a contribution arising from the International Polar Year Circumpolar Flaw Lead System Study project.

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NATALIE C. ASSELIN, (1), (2) DAVID G. BARBER, (1) PIERRE R. RICHARD (3) and STEVEN H. FERGUSON (3)

(1.) Centre for Earth Observation Science, Department of Environment and Geography, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada

(2.) Corresponding author; present address: Wapusk National Park and Manitoba North National Historic Sites, Parks Canada, Box 127, Churchill, Manitoba ROB 0E0, Canada; natalie.asselin@pc.gc.ca

(3.) Fisheries and Oceans Canada, 501 University Crescent, Winnipeg, Manitoba R3T 2N6, Canada

[C] The Arctic Institute of North America

(Received 10 May 2011; accepted in revised form 2 November 2011)
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