Changes in climate are rapidly modifying the Arctic environment. As a result, human activities—and the sounds they produce—are predicted to increase in remote areas of Greenland, such as those inhabited by the narwhals (Monodon monoceros) of East Greenland. Meanwhile, nothing is known about these whales’ acoustic behavior or their reactions to anthropogenic sounds. This lack of knowledge was addressed by instrumenting six narwhals in Scoresby Sound (Aug 2013–2016) with Acousonde™ acoustic tags and satellite tags. Continuous recordings over up to seven days were used to describe the acoustic behavior of the whales, in particular their use of three types of sounds serving two different purposes: echolocation clicks and buzzes, which serve feeding, and calls, presumably used for social communication. Logistic regression models were used to assess the effects of location in time and space on buzzing and calling rates. Buzzes were mostly produced at depths of 350–650 m and buzzing rates were higher in one particular fjord, likely a preferred feeding area. Calls generally occurred at shallower depths (<100 m), with more than half of these calls occurring near the surface (<7 m), where the whales also spent more than half of their time. A period of silence following release, present in all subjects, was attributed to the capture and tagging operations, emphasizing the importance of longer (multi-day) records. This study provides basic life-history information on a poorly known species—and therefore control data in ongoing or future sound-effect studies.

One of the last pristine marine soundscapes, the Arctic, is exposed to increasing anthropogenic activities due to climate-induced decrease in sea ice coverage. In this study, we combined movement and behavioral data from animal-borne tags in a controlled sound exposure study to describe the reactions of narwhals, Monodon monoceros, to airgun pulses and ship noise. Sixteen narwhals were live captured and instrumented with satellite tags and Acousonde acoustic-behavioral recorders, and 11 of them were exposed to airgun pulses and vessel sounds. The sound exposure levels (SELs) of pulses from a small airgun (3.4 L) used in 2017 and a larger one (17.0 L) used in 2018 were measured using drifting recorders. The experiment was divided into trials with airgun and ship-noise exposure, intertrials with only ship-noise, and pre- and postexposure periods. Both trials and intertrials lasted ∼4 h on average per individual. Depending on the location of the whales, the number of separate exposures ranged between one and eight trials or intertrials. Received pulse SELs dropped below 130 dB re 1 μPa2 s by 2.5 km for the small airgun and 4–9 km for the larger airgun, and background noise levels were reached at distances of ∼3 and 8–10.5 km, respectively, for the small and big airguns. Avoidance reactions of the whales could be detected at distances &gt;5 km in 2017 and &gt;11 km in 2018 when in line of sight of the seismic vessel. Meanwhile, a ∼30% increase in horizontal travel speed could be detected up to 2 h before the seismic vessel was in line of sight. Applying line of sight as the criterion for exposure thus excludes some potential pre-response effects, and our estimates of effects must therefore be considered conservative. The whales reacted by changing their swimming speed and direction at distances between 5 and 24 km depending on topographical surroundings where the exposure occurred. The propensity of the whales to move towards the shore increased with increasing exposure (i.e., shorter distance to vessels) and was highest with the large airgun used in 2018, where the whales moved towards the shore at distances of 10–15 km. No long-term effects of the response study could be detected.

The effects of climate change constitute a major concern in Arctic waters due to the rapid decline of sea ice, which may strongly alter the movements and habitat availability of Arctic marine mammals. We tracked 98 bowhead whales by satellite over an 11-year period (2001–2011) in Baffin Bay - West Greenland to investigate the environmental drivers (specifically sea surface temperature and sea ice) involved in bowhead whale’s movements. Movement patterns differed according to season, with aggregations of whales found at higher latitudes during spring and summer likely in response to sea-ice retreat and increasing sea temperature (SST) facilitated by the warm West Greenland Current. In contrast, the whales moved further south in response to sea temperature decrease during autumn and winter. Statistical models indicated that the whales targeted a narrow range of SSTs from −0.5 to 2 °C. Sea surface temperatures are predicted to undergo a marked increase in the Arctic, which could expose bowhead whales to both thermal stress and altered stratification and vertical transport of water masses. With such profound changes, bowhead whales may face extensive habitat loss. Our results highlight the need for closer investigation and monitoring in order to predict the extent of future distribution changes.

Singing behavior has been described from bowhead whales in the Bering Sea during their annual spring migration and from Davis Strait during their spring feeding season. It has been suggested that this spring singing behavior is a remnant of the singing during the winter breeding season, though no winter recordings are available. In this study, the authors describe recordings made during the winter and spring months of bowhead whales in Disko Bay, Western-Greenland. A total of 7091 bowhead whale sounds were analyzed to describe the vocal repertoire, the singing behavior, and the changes in vocal behavior from February to May. The vocal signals could be divided into simple (frequency-modulated) calls (n=483), complex (amplitude-modulated) calls (n=635), and song notes (n=5973). Recordings from the end of February to middle of March were characterized by higher call rates with a greater diversity of call types than recordings made later in the season. This study is the first description of bowhead song from the stock in Western-Greenland during both the winter and spring months, and provides support for the hypothesis that song during the winter months contains more song notes than song from the spring making the winter song more variable.

The vertical distribution and in situ egg production of Calanus finmarchicus and C. glacialis were studied in Disko Bay, western Greenland, from winter throughout the spring bloom. The 2 species entered the surface water simultaneously, but their spawning patterns differed significantly. Maximum egg production for C. glacialis of 48 ± 8 eggs female -1 d -1 was measured on May 1, 2005 in association with the culmination of the bloom, while the highest egg production rate of C. finmarchicus of 44 ± 7 eggs female -1 d -1 was measured on May 25 after termination of the bloom. During 3 phases of the spring bloom, the impact of starvation and saturating food conditions on the egg production rates of the 2 Calanus species was investigated in the laboratory. Experiments with starved and ad libitum fed females showed a significant difference in the egg production rate between the 2 species, depending on sampling time, i.e. gonad maturity and feeding history. The results showed varying use of saturating food during the 3 phases of the bloom. For C. finmarchicus, no effect of food was observed during the first experiment in late April, whereas females collected in early May, during the peak of the spring bloom, responded strongly to changes in food concentration, with egg production which was 3 times higher than that of the starved controls. In contrast, C. glacialis responded strongly to food concentration in both late April and early May. The present investigations illustrate that Calanus females from the Disko Bay area continue to produce eggs without food more than twice as long as those reported from other northern populations. This observation could indicate an adaptation to the Disko Bay environment, which has unpredictable ice conditions and consequently large variations in the initiation of the spring bloom.