Marine mammal detections on the Chukchi Plateau 2009-2020.

The Arctic Ice Monitoring (AIM) observatory has been maintained on the Chukchi Plateau at 75.1° N 168.0° W nearly continuously since 2003. The AIM site consists of a submerged mooring that, since October 2008, has been instrumented with a passive acoustic recorder to sample ambient sound, with a focus on marine mammal detections in the High Arctic. Year-long data sets for 2009, 2012, and 2014-2020 were analyzed for the presence of signals from Arctic species including bowhead and beluga whales, bearded seals, and walrus. Calls from subarctic ribbon seals were commonly detected in autumn months, suggesting they have expanded their distribution much further northward. Killer whale calls were detected in recent years providing evidence that they have moved further north into the Pacific Arctic. No other subarctic cetaceans were heard. Year-round passive acoustic sampling of sounds produced by marine mammals over a decadal timescale has enhanced our understanding of how climate-driven changes in biodiversity are affecting even the very High Arctic.

Call repertoire and inferred ecotype presence of killer whales (Orcinus orca) recorded in the southeastern Chukchi Sea.

Killer whales occur in the Arctic but few data exist regarding the ecotypes present. The calling behavior differs among ecotypes, which can be distinguished based on pulsed call type, call rate, and bandwidth. In this study, a passive acoustic recorder was deployed 75 km off Point Hope, Alaska, in the southeastern Chukchi Sea to identify which ecotypes were present. A total of 1323 killer whale pulsed calls were detected on 38 of 276 days during the summers (June-August) of 2013-2015. The majority of calls (n = 804, 61%) were recorded in 2013 with the most calls recorded in July (76% of total calls). The calls were manually grouped into six categories: multipart, downsweep, upsweep, modulated, single modulation, and flat. Most detections were flat (n = 485, 37%) or multipart calls (n = 479, 36%), which contained both high and low frequency components. Call comparisons with those reported in the published literature showed similarities with other transient populations in fundamental frequency contour point distribution and median frequency. This study provides the first comprehensive catalog of transient killer whale calls in this region as well as reports on previously undescribed calls.

Bounding the number of calling animals with passive acoustics and reliable locations.

When n animal calls are passively detected at n different times, the number of animals producing the sounds is anywhere between one and n unless more information is available. When extremely reliable confidence intervals of location are also available for each call, the upper bound is still n, but a lower bound can be derived. The lower bound exceeds one when it is physically impossible for an animal to travel quickly enough to go from one reliable location to another within the temporal call interval. When many calls are detected, it may be too complicated or numerically prohibitive to determine the minimum number of animals responsible for the calls in space and time by inspection or brute force methods. Instead, it is advantageous to use graph theory. The lower bound for the number of calling animals can be derived using 100% confidence intervals of each call's location. Mathematical theorems guarantee the lower bound is correct: a lesser value is impossible to obtain. Guaranteed bounds for the abundance of calling animals are useful for conservation in the presence of environmental stress and studying behavior.

Estimating acoustic cue rates in bowhead whales, Balaena mysticetus, during their fall migration through the Alaskan Beaufort Sea.

Eight years of passive acoustic data (2007-2014) from the Beaufort Sea were used to estimate the mean cue rate (calling rate) of individual bowhead whales (Balaena mysticetus) during their fall migration along the North Slope of Alaska. Calls detected on directional acoustic recorders (DASARs) were triangulated to provide estimates of locations at times of call production, which were then translated into call densities (calls/h/km2). Various assumptions were used to convert call density into animal cue rates, including the time for whales to cross the arrays of acoustic recorders, the population size, the fraction of the migration corridor missed by the localizing array system, and the fraction of the seasonal migration missed because recorders were retrieved before the end of the migration. Taking these uncertainties into account in various combinations yielded up to 351 cue rate estimates, which summarize to a median of 1.3 calls/whale/h and an interquartile range of 0.5-5.4 calls/whale/h.

Exploring movement patterns and changing distributions of baleen whales in the western North Atlantic using a decade of passive acoustic data.

Six baleen whale species are found in the temperate western North Atlantic Ocean, with limited information existing on the distribution and movement patterns for most. There is mounting evidence of distributional shifts in many species, including marine mammals, likely because of climate-driven changes in ocean temperature and circulation. Previous acoustic studies examined the occurrence of minke (Balaenoptera acutorostrata) and North Atlantic right whales (NARW; Eubalaena glacialis). This study assesses the acoustic presence of humpback (Megaptera novaeangliae), sei (B. borealis), fin (B. physalus), and blue whales (B. musculus) over a decade, based on daily detections of their vocalizations. Data collected from 2004 to 2014 on 281 bottom-mounted recorders, totaling 35,033 days, were processed using automated detection software and screened for each species' presence. A published study on NARW acoustics revealed significant changes in occurrence patterns between the periods of 2004-2010 and 2011-2014; therefore, these same time periods were examined here. All four species were present from the Southeast United States to Greenland; humpback whales were also present in the Caribbean. All species occurred throughout all regions in the winter, suggesting that baleen whales are widely distributed during these months. Each of the species showed significant changes in acoustic occurrence after 2010. Similar to NARWs, sei whales had higher acoustic occurrence in mid-Atlantic regions after 2010. Fin, blue, and sei whales were more frequently detected in the northern latitudes of the study area after 2010. Despite this general northward shift, all four species were detected less on the Scotian Shelf area after 2010, matching documented shifts in prey availability in this region. A decade of acoustic observations have shown important distributional changes over the range of baleen whales, mirroring known climatic shifts and identifying new habitats that will require further protection from anthropogenic threats like fixed fishing gear, shipping, and noise pollution.

Song production by the North Pacific right whale, Eubalaena japonica.

This paper describes song production by the eastern North Pacific right whale (NPRW, Eubalaena japonica) in the southeastern Bering Sea. Songs were localized in real-time to individuals using sonobuoys. Singers whose sex could be determined were all males. Autonomous recorder data from 17 year-long deployments were analyzed to document and characterize song types. Four distinct song types were documented over eight years (2009-2017) at five distinct locations. Each song type consists of a hierarchical structure of 1-3 different repeating phrases comprised predominantly of gunshot sounds; three of the four songs contained additional sound types (downsweep, moan, and low-frequency pulsive call). Songs were detected annually (July-January); all song types remained consistent over eight years. Two different songs often occurred simultaneously, produced by different individuals; the same song was never detected simultaneously at the same location. The same song type was detected on the same day and time at two distant locations, indicating multiple individuals can produce the same song. These findings provide support that males produce song; it remains unknown if females also sing. NPRW is the first right whale species documented to produce song. Based on current knowledge about song in mysticetes, it is hypothesized that these songs are reproductive displays.

Using nonlinear time warping to estimate North Pacific right whale calling depths in the Bering Sea.

Calling depth distributions are estimated for two types of calls produced by critically endangered eastern North Pacific right whales (NPRWs) in the Bering Sea, using passive acoustic data collected with bottom-mounted hydrophone recorders. Nonlinear time resampling of 12 NPRW "upcalls" and 20 "gunshots" recorded in a critical NPRW habitat isolated individual normal mode arrivals from each call. The relative modal arrival times permitted range estimates between 1 and 40 km, while the relative modal amplitudes permitted call depth estimates, provided that environmental inversions were obtained from high signal-to-noise ratio calls. Gunshot sounds were generally only produced at a few meters depth, while upcall depths clustered between 10 and 25 m, consistent with previously published bioacoustic tagging results from North Atlantic right whales. A Wilcoxon rank sum test rejected the null hypothesis that the mean calling depths of the two call types were the same (p = 2.9 × 10-5); the null hypothesis was still rejected if the sample set was restricted to one call per acoustic encounter (p = 0.02). Propagation modeling demonstrates that deeper depths enhance acoustic propagation and that source depth estimates impact both NPRW upcall source level and detection range estimates.

Beluga whale (Delphinapterus leucas) vocalizations and call classification from the eastern Beaufort Sea population.

Beluga whales, Delphinapterus leucas, have a graded call system; call types exist on a continuum making classification challenging. A description of vocalizations from the eastern Beaufort Sea beluga population during its spring migration are presented here, using both a non-parametric classification tree analysis (CART), and a Random Forest analysis. Twelve frequency and duration measurements were made on 1019 calls recorded over 14 days off Icy Cape, Alaska, resulting in 34 identifiable call types with 83% agreement in classification for both CART and Random Forest analyses. This high level of agreement in classification, with an initial subjective classification of calls into 36 categories, demonstrates that the methods applied here provide a quantitative analysis of a graded call dataset. Further, as calls cannot be attributed to individuals using single sensor passive acoustic monitoring efforts, these methods provide a comprehensive analysis of data where the influence of pseudo-replication of calls from individuals is unknown. This study is the first to describe the vocal repertoire of a beluga population using a robust and repeatable methodology. A baseline eastern Beaufort Sea beluga population repertoire is presented here, against which the call repertoire of other seasonally sympatric Alaskan beluga populations can be compared.

Changes in gray whale phenology and distribution related to prey variability and ocean biophysics in the northern Bering and eastern Chukchi seas.

Changes in gray whale (Eschrichtius robustus) phenology and distribution are related to observed and hypothesized prey availability, bottom water temperature, salinity, sea ice persistence, integrated water column and sediment chlorophyll a, and patterns of wind-driven biophysical forcing in the northern Bering and eastern Chukchi seas. This portion of the Pacific Arctic includes four Distributed Biological Observatory (DBO) sampling regions. In the Bering Strait area, passive acoustic data showed marked declines in gray whale calling activity coincident with unprecedented wintertime sea ice loss there in 2017-2019, although some whales were seen there during DBO cruises in those years. In the northern Bering Sea, sightings during DBO cruises show changes in gray whale distribution coincident with a shrinking field of infaunal amphipods, with a significant decrease in prey abundance (r = -0.314, p<0.05) observed in the DBO 2 region over the 2010-2019 period. In the eastern Chukchi Sea, sightings during broad scale aerial surveys show that gray whale distribution is associated with localized areas of high infaunal crustacean abundance. Although infaunal crustacean prey abundance was unchanged in DBO regions 3, 4 and 5, a mid-decade shift in gray whale distribution corresponded to both: (i) a localized increase in infaunal prey abundance in DBO regions 4 and 5, and (ii) a correlation of whale relative abundance with wind patterns that can influence epi-benthic and pelagic prey availability. Specifically, in the northeastern Chukchi Sea, increased sighting rates (whales/km) associated with an ~110 km (60 nm) offshore shift in distribution was positively correlated with large scale and local wind patterns conducive to increased availability of krill. In the southern Chukchi Sea, gray whale distribution clustered in all years near an amphipod-krill 'hotspot' associated with a 50-60m deep trough. We discuss potential impacts of observed and inferred prey shifts on gray whale nutrition in the context of an ongoing unusual gray whale mortality event. To conclude, we use the conceptual Arctic Marine Pulses (AMP) model to frame hypotheses that may guide future research on whales in the Pacific Arctic marine ecosystem.

Long-term passive acoustic recordings track the changing distribution of North Atlantic right whales (Eubalaena glacialis) from 2004 to 2014.

Given new distribution patterns of the endangered North Atlantic right whale (NARW; Eubalaena glacialis) population in recent years, an improved understanding of spatio-temporal movements are imperative for the conservation of this species. While so far visual data have provided most information on NARW movements, passive acoustic monitoring (PAM) was used in this study in order to better capture year-round NARW presence. This project used PAM data from 2004 to 2014 collected by 19 organizations throughout the western North Atlantic Ocean. Overall, data from 324 recorders (35,600 days) were processed and analyzed using a classification and detection system. Results highlight almost year-round habitat use of the western North Atlantic Ocean, with a decrease in detections in waters off Cape Hatteras, North Carolina in summer and fall. Data collected post 2010 showed an increased NARW presence in the mid-Atlantic region and a simultaneous decrease in the northern Gulf of Maine. In addition, NARWs were widely distributed across most regions throughout winter months. This study demonstrates that a large-scale analysis of PAM data provides significant value to understanding and tracking shifts in large whale movements over long time scales.

St. Lawrence blue whale vocalizations revisited: characterization of calls detected from 1998 to 2001.

From 1998 to 2001, 115 h of acoustic recordings were made in the presence of the well-studied St. Lawrence population of blue whales, using a calibrated omnidirectional hydrophone [flat (+/- 3 dB) response from 5 to 800 Hz] suspended at 50 m depth from a surface isolation buoy. The primary field site for this study was the estuary region of the St. Lawrence River (Québec, Canada), with most recordings made between mid-August and late October. During the recordings, detailed field notes were taken on all cetaceans within sight. Characterization of the more than 1000 blue whale calls detected during this study revealed that the St. Lawrence repertoire is much more extensive than previously reported. Three infrasonic (<20 Hz) and three audible range (30-200 Hz) call types were detected, with much time/frequency variation seen within each type. Further variation is seen in the form of call segmentation, which appears (through examination of Lloyd's Mirror interference effects) to be controlled at least partially by the whales. Although St. Lawrence blue whale call characteristics are similar to those of the North Atlantic, comparisons of phrase composition and spacing among studies suggest the possibility of population dialects within the North Atlantic.