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Article

Insights into Blue Whale (Balaenoptera musculus L.) Population Movements in the Galapagos Archipelago and Southeast Pacific

by
Hector M. Guzman
1,
Rocío M. Estévez
1 and
Stefanie Kaiser
2,*,†
1
Naos Marine Laboratory, Smithsonian Tropical Research Institute, Panama City P.O. Box 0843-03092, Panama
2
Senckenberg Research Institute and Natural History Museum, 60325 Frankfurt am Main, Germany
*
Author to whom correspondence should be addressed.
†
Current address: Department of Invertebrate Zoology and Hydrobiology, University of Lodz, 90-237 Łódź, Poland.
Animals 2024, 14(18), 2707; https://doi.org/10.3390/ani14182707
Submission received: 12 July 2024 / Revised: 6 September 2024 / Accepted: 11 September 2024 / Published: 18 September 2024
(This article belongs to the Section Ecology and Conservation)
Browse Figures
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Abstract

:

Simple Summary

The Galapagos Marine Reserve supports cetaceans such as blue whales by providing essential foraging areas and resting areas. From 2021 to 2023, a study utilized satellite tags on 16 blue whales to monitor their movements and gain insights into their interactions with the marine environment. This involved the identification of their feeding grounds, indicated by chlorophyll levels, surface water temperature (SST), and ocean productivity. The study revealed that blue whales prefer areas with presumed increased prey abundance, cooler water temperatures, and specific underwater features such as ridges that likely enhance favored food sources. Most of the tagged whales remained in the Galapagos, particularly near Isabela Island, where there is an elevated risk of collisions with boats due to increased marine traffic. Some whales ventured into Ecuador’s waters, and one even traveled to Peru. In 2023, an intense El Niño event led to changes in water temperatures and food availability, significantly impacting whale habitats. This research contributes to efforts to protect whales from ship collisions and understand and adapt to changes in their migration patterns due to climate variations.

Abstract

The Galapagos Marine Reserve is vital for cetaceans, serving as both a stopover and residency site. However, blue whales, occasionally sighted here, exhibit poorly understood migratory behavior within the Galapagos and the broader Eastern Tropical Pacific. This study, the first to satellite tag blue whales in the Galapagos (16 tagged between 2021 and 2023), explored their behavior in relation to environmental variables like chlorophyll-a concentration, sea surface temperature (SST), and productivity. Key findings show a strong correlation between foraging behavior, high chlorophyll-a levels, productivity, and lower SSTs, indicating a preference for food-rich areas. Additionally, there is a notable association with geomorphic features like ridges, which potentially enhance food abundance. Most tagged whales stayed near the Galapagos archipelago, with higher concentrations observed around Isabela Island, which is increasingly frequented by tourist vessels, posing heightened ship strike risks. Some whales ventured into Ecuador’s exclusive economic zone, while one migrated southward to Peru. The strong 2023 El Niño–Southern Oscillation event led to SST and primary production changes, likely impacting whale resource availability. Our study provides crucial insights into blue whale habitat utilization, informing adaptive management strategies to mitigate ship strike risks and address altered migration routes due to climate-driven environmental shifts.

1. Introduction

Escalating and cumulative impacts of human activities on oceanic ecosystems, such as overexploitation, habitat destruction, pollution, and climate change, pose considerable threats to marine biodiversity, leading to notable population declines and pushing numerous species toward extinction [1,2]. As awareness of the importance of healthy oceans grows, protecting biodiversity and its critical ecosystem services, such as food provisioning and carbon sequestration, has become essential for maintaining ecosystem stability and resilience [3,4,5]. The effective conservation of marine biodiversity requires mapping and understanding species distributions and the environmental factors affecting them. However, most marine species still require further study [6]. Remarkably, this trend extends even to the largest marine species, the blue whale (Balaenoptera musculus L.), whose migratory behavior across vast oceanic spaces complicates efforts to accurately assess population numbers and distributions [7].
Currently, B. musculus is classified as endangered according to the International Union for Conservation of Nature (IUCN) Red List of Threatened Species [8]. Decades of intensive commercial whaling during the 20th century decimated their populations, especially in the Southern Ocean, pushing them to the brink of extinction [9,10]. Although some regions show signs of recovery, populations remain well below pre-whaling levels [9,10,11]. Taxonomic uncertainties, distribution challenges, and limited data on seasonal movements due to variable monitoring efforts impede global and regional population assessments [10,12,13,14].
Worldwide, two to four subspecies within B. musculus have been distinguished morphologically, genetically, and geographically [15,16]. In the Southern Hemisphere, these include the Antarctic blue whale, B. m. intermedia, and the Pygmy blue whale, B. m. brevicauda [17]. In the Northern Hemisphere, B. m. indica occupies the North Indian Ocean, and B. m. musculus is found in the North Atlantic and North Pacific oceans [18,19]. Taxonomic uncertainty persists for B. m. brevicauda and B. m. indica, with differentiation primarily based on song types [18,19]. In the Eastern South Pacific, a potentially distinct population or subspecies known as the Chilean blue whale has been suggested to exist, though formal recognition is pending [10,14,20]. These subspecies are further divided into populations based on migration routes, regions, and song types, with vocalizations identifying eleven distinct vocal populations globally [12,21,22,23,24,25,26,27].
The conventional understanding is that blue whales alternate between high-latitude nutrient-rich waters to feed almost exclusively on euphausiids (krill) during the summer and low-latitude breeding grounds during the winter [28,29,30]. However, sightings, captures, and acoustic evidence suggest a year-round presence at various latitudes, challenging this paradigm [31,32,33,34]. Deviations from this pattern can lead to more opportunities for different populations to co-occur in the same location [26,35,36].
The Eastern Tropical Pacific (ETP), located between the subtropical gyres of the North and South Pacific, is a shared wintering area for blue whales from the Northeast Pacific (NEP) and Southeast Pacific (SEP) populations [14]. Whales primarily aggregate around Baja California, the Thermal Dome (previously described as the Costa Rica Dome), offshore Peru, and the Galapagos archipelago [14,29]. Comprehensive data on movements and habitat use within the ETP are limited due to the rarity of sightings and challenges in studying these remote areas [36]. The Thermal Dome is believed to be a breeding area for NEP whales, while the Galapagos Marine Reserve is a significant wintering and potential breeding area for SEP whales [23,29,31,37,38]. There is, however, evidence of a year-round blue whale population in the Galapagos [35], as well as the co-occurrence of NEP and SEP migratory populations [39].
Blue whale sightings in the Galapagos are year-round, though they are rare, with no more than 65 sightings reported over the last two decades [29,36]. However, they have recently increased due to citizen science programs [36,40]. This study aims to provide additional insights into the migratory behavior of blue whales in the Galapagos region, exploring whether their year-round presence is due to non-migratory residents or seasonal visitors from the NEP or SEP populations [36]. Satellite tags were deployed on B. musculus individuals in the Galapagos over three years. By analyzing the tracked movements of these whales alongside remote sensing data on oceanographic parameters, the study seeks to uncover factors driving their migration patterns and explore population interconnections. During the tagging years, we conducted an analysis of El Niño–Southern Oscillation (ENSO) conditions to provide an explanation for the presence of the whales in the archipelago. The findings are expected to inform conservation and management strategies by enhancing our understanding of how oceanographic conditions affect whale distribution and behavior within the Galapagos and the broader ETP.

2. Materials and Methods

2.1. Tagging Procedures

Sixteen blue whales were tagged in the Galapagos archipelago, ten in 2021, four in 2022, and two in 2023 (Table 1). A transdermal satellite transmitter model SPOT-372A manufactured by Wildlife Computers (Redmond, WA, USA) was used. The tag model used specifies a battery life of 540 days, assuming 250 Argos transmissions per day. Factory transmitters are 293 mm in length and 24 mm in diameter for the stainless-steel tube case and weigh 390 g, coupled to a stainless-steel spear with a 3 cm triangular double-edged blade tip containing three pairs of 5 cm barbs placed at 90° to each other.
To maximize battery life, transmitters were programmed to limit transmissions to a time block from 01:00 to 22:00 h every 2 days and to slow the repetition rate after 10 consecutive dry transmissions. Tags were chemically sterilized and plastic-wrapped in the laboratory. Before deployment, the tag/spear was sprayed with the antibiotic Neomycin Sulfate—Clostebol Acetato (Neobol®, Luminova Pharma Group, Guatemala City, Guatemala). The Animal Care and Use Committee of the Smithsonian Tropical Research Institute approved the procedure.
Whales were tagged from a long fiberglass-hull inflatable boat at approximately 2–4 m. Tags were deployed using an ARTS pneumatic line-thrower (Restech Inc., Bodø, Norway) coupled to a carrier/launching tube (Wildlife Computers, Redmond, WA, USA). A detailed description of the tagging procedure is provided elsewhere [41,42].

2.2. Track Correction and Environmental Covariates

The tag-derived positions from Argos satellite location classes “3”, “2”, “1”, “0”, “A”, and “B” were used with a range of errors in accuracy estimated to be between a 150 m and 5 km radius for plotting general filtered whale movements (see [43,44]). The location classes represent different levels of positional accuracy, where the standard quality signals of “3”, “2”, and “1” are derived from four or more messages and the low-quality locations are classes “0”, “A”, “B”, and “Z”, derived from three or two messages considered less accurate [45]. Raw transmissions were filtered to avoid unrealistic traveling speeds faster than 3 m s−1 [46], as well as transmissions occurring on land and with an Argos quality of “Z”. Density distribution within the insular exclusive economic zone of Ecuador, including the Galapagos Marine Reserve, was assessed using kernel density plots to understand whale habitat utilization. The analysis categorized areas into the following three tiers: low-use areas, representing regions from the smallest values (excluding 0) up to the first quartile (25% of the utilized habitat); intermediate-use areas, spanning from the first to the third quartiles (50% of the utilized habitat); and high-use areas, comprising values above the third quartile (representing 75% of the utilized habitat). For the kernel density estimation, the output cell size was manually set to 0.01 to improve the raster resolution, the search radius was automatically determined using the software to optimize the spatial resolution of the density estimation, and the EEZ (exclusive economic zone) was used as a boundary to ensure the analysis was constrained to the study area. Data analyses and visualization were conducted using the spatial analyst tool in ArcGIS Pro V3.2 (ESRI).
We used a state–space model to analyze whale movements to correct for errors derived from the Argos satellite tracking data. In addition, it allowed us to interpret the behavior of the whales at each individual location. We used movement persistence, an index of movement behavior that can be estimated as a continuous-valued variable (ranging from 0 to 1) which is time-varying, representing changes in the movement pattern based on autocorrelation in speed and direction [47]. We employed the “fit_ssm()” approach with the “model = mp” option to estimate move persistence accurately. This approach consists of fitting a continuous-time state–space model of motion persistence (MP), which allows us to infer the actual locations and the degree of motion persistence. We selected this method because it effectively handles the irregular timing and error-prone nature of telemetry data from the Argos satellite system while still capturing key behavioral patterns in whale movement [48]. We used the “fit_ssm” function from the aniMotum package [48] in R version 4.2.3 [49] with a speed filter threshold of 3 m s−1 [33] and a 6 h time step.
Estimated locations based on the state–space model results were analyzed with a hidden Markov model (HMM) to identify different behavioral states and correlate them to environmental variables. The HMM model was run using the function “fitHMM”, available in the R package moveHMM [50]. Initial values were set to 60 ± 10 km for migratory behavior, 20 ± 10 km for foraging behavior, and π to 0 for the turning angle, considering data availability and whale speed [33] (Table 2). Monthly chlorophyll-a concentration, 3-day composite productivity, and daily sea surface temperature were used as model covariates and were obtained from the NOAA’s Environmental Research Division ERDDAP server (NOAA ERDDAP, 2023). The temporal and spatial pairing between estimated locations and environmental data was performed using the R software “xtracto” function in the xtractomatic package [51]. To examine the possible correlations between the environmental variables, a correlation matrix was calculated using R software. A Wilcoxon rank-sum test was employed to investigate the relationship between chlorophyll (Chl), primary production (Prod), sea surface temperature (SST), and the different states of foraging and migration. This test was carried out with a significance threshold of 0.05 to determine if there was a statistically significant association between Chl, Prod, SST, and the foraging and migration states.
To describe the distribution as a function of depth, bathymetric data were obtained from the GEBCO dataset [52]. The bathymetric map was created in ArcGIS Pro v3.2, employing the shaded relief tool and overlaid with the hidden Markov model (HMM) result. To assess the statistical differences in depth between these two behaviors, a Wilcoxon rank-sum test was performed using R v4.2.3. Depth data ranges were divided into five arbitrary depth categories, and each modeled transmission was assigned to one of these ranges.

2.3. El Niño–Southern Oscillation

We used daily satellite data from the Copernicus Marine Service to assess the impact of the ENSO on critical oceanographic conditions in the Galapagos archipelago during our whale tagging expeditions [53,54,55,56]. These data spanned the period from 2020 to 2023 and included various oceanographic parameters essential to the study, such as chlorophyll concentration, primary productivity, and sea surface temperature. This analysis aimed to determine whether ENSO-related environmental changes, such as reduced chlorophyll and productivity, along with higher sea surface temperatures, may have contributed to the observed reduction in whale sightings during 2023.
The acquired satellite data underwent preprocessing steps to enhance their suitability for analysis. Initially, the raw daily data were filtered to reduce noise and variability by computing quarterly averages. This averaging process facilitated the extraction of seasonal trends and mitigated the effects of short-term fluctuations.
A rectangular zone extending 200 nautical miles from the outermost edges of the archipelago was delineated for analysis. The preprocessed satellite data for each year were imported into ArcGIS Pro version 3.2 for visualization and spatial analysis.
To further assess the ENSO phenomenon, the Oceanic Niño Index (ONI) was evaluated and visualized for the four-year period under study. The ONI data were sourced from the NOAA Climate Prediction Center, which provides information on warm and cold periods based on a threshold of ±0.5 °C for the ONI. The ONI is derived from the 3-month running mean of ERSSTv5 sea surface temperature (SST) anomalies in the Niño 3.4 region (5° N–5° S, 120°–170° W). The ONI for the period from 2020 to 2023 was plotted using the “ggplot2” package in R version 4.2.3.

3. Results

All blue whales were tagged during the austral winter season (May–October), specifically during the period with the highest number of sightings [36]. Sixteen blue whales made substantial journeys in various directions from their initial point of tagging during three different years, which were 2021, 2022, and 2023. The maximum distance covered was approximately 2400 km over a span of 98 days. This translates to an average speed of 25 km per day or 1 km per hour. The kernel density analysis identified regions of high-density usage around the Galapagos Islands and southwest of Ecuador’s exclusive economic zone (EEZ). Medium-density zones were observed in the southwestern vicinity of the islands, contiguous with the high-density areas in the south of the EEZ, while low-density regions were predominantly situated around the islands and in the southern expanse of the EEZ (Figure 1). On average, whales spent 22.98 ± 37.7 (54 maximum; 1.9 minimum) days inside the Galapagos’ EEZ (Table 1).
After track correction using the state–space model, successful modeling was achieved for 15 of the 16 whales, as whale ID 228114 could not be modeled due to less than 10 transmissions of good quality within 15 days. The initial database, which encompassed all whales, comprised 5990 Argos locations classified into error classes as follows (in descending order): B (62.68%), A (18.14%), 0 (7.18%), 1 (6.94%), 2 (2.74%), 3 (1.77%), and Z (0.55%). Following track correction of the state–space model, the database increased to 3448 coordinate locations (Figure 2).

3.1. Identification of Behavioral States and Their Relationship with Environmental Variables

The hidden Markov model (HMM) could be applied to eight (whales id: 178968, 196850, 196852, 196854, 196855, 196856, 228115, and 228119) of the sixteen whales originally tagged because of the extent and nature of the data, as many of these whales transmitted for longer periods. The model delineated two distinct behavioral states, namely migrating, characterized by a step distance (distance between time intervals) of 25.12 km (±15.16 km) and a turning angle of about 0.002 radians, and foraging, characterized by a step distance of 7.06 km (±5.07 km) and a turning angle of approximately −0.086 radians (Figure 3). The swimming patterns during foraging indicate an effort to remain within a prey patch, while migration travel behaviors involve movement between patches.
Whales used different zones for foraging based on bathymetry. It was observed that whales appeared to travel south from the Galapagos Islands along the continental shelf margin, creating a significant foraging hotspot at the convergence of the continental shelf with the Nazca Ridge. Additionally, whales seemed to travel adjacent to ridges, with a notable feeding area at the intersection of the Carnegie Ridge and the continental shelf. This pattern indicated several feeding zones around the Galapagos Islands, the Nazca Ridge, and other regions, highlighting a strong link between bathymetric features and foraging behavior (Figure 3). Statistical analysis confirms significant differences in depth between feeding and migrating states (W = 204,191, p < 0.05). Whales tended to feed in deeper waters compared to when they were migrating. Specifically, 82.30% of the foraging locations were in waters deeper than 1500 m, whereas only 70.55% of the locations during migration were in similarly deep waters (Table 3).
The likelihood of transitioning between these behavioral states (from migrating to foraging or vice versa) exhibited correlations with local environmental conditions under stationary long-term distribution (i.e., a stable pattern of behavioral states over an extended period) (Table 4). Specifically, the probability of a whale being in a foraging state increased as chlorophyll and primary productivity rose and decreased as sea surface temperature levels rose, while the probability of being in a migratory state decreased with increasing Prod and Chl, and increased with increasing SST (Figure 4A–C).
The correlation matrix for environmental variables showed that there were no relationships between them. Tracked whales predominantly occupied waters with Chl levels averaging 0.81 ± 1.53 mg m−3, a Prod of 1410.96 ± 2892.40 mg C m2 day−1, and a SST of 21.69 ± 1.59 °C. There was a significant contrast in Chl, Prod, and SST levels between behavioral states. When blue whales were foraging, the Chl levels were notably higher (0.97 mg m−3) compared to when they were in the migrating state (0.72 mg m−3) (W = 250,233, p < 0.05, Figure 5A). In the case of Prod, blue whales demonstrated a preference for areas with higher productivity, recording 1839.55 mg C m2 day−1 during foraging compared to 1201.48 mg C m2 day−1 during migratory behavior (W = 54,912, p < 0.05, Figure 5B). Sea surface temperature (SST) differed significantly between the two behavioral states. During migration, the average SST was 21.8 °C, while during foraging, it was 21.5 °C (W = 187,499, p < 0.05, Figure 5C).

3.2. El Niño–Southern Oscillation

Fewer whales were observed and consequently tagged in 2023 during the El Niño event, even considering that the yearly field effort was nearly three times that of the previous two expeditions. Chlorophyll in 2023 was lower than in previous years (2020, 2021, and 2022). In 2020, the maximum chlorophyll peak occurred between July and September, with a maximum of 13.18 mg m−3, and the period with the lowest chlorophyll was between October and December, with a maximum of 1.85 mg m−3. In contrast, in 2021, the highest chlorophyll concentration occurred from October to December, reaching 10.16 mg m−3, while the lowest concentration was 0.97 mg m−3 between April and June. In 2022, the highest chlorophyll levels were also from October to December, with a maximum of 18.26 mg m−3, while the lowest levels were recorded between July and September, at 5.78 mg m−3. Finally, in 2023, the highest chlorophyll concentration was 8.45 mg m−3 between January and March, and the lowest was between October and December, with a maximum of 0.83 mg m−3 (Figure 6). Coinciding with chlorophyll, primary productivity was lower in 2023 compared to the previous three years. In 2020, the maximum primary productivity was between July and September, with 2809 mg C m−2, and the minimum was between January and March, with a 1466 mg C m−2 peak. In 2021, the maximum was in the first four-month period of the year, with a maximum of 2122 mg C m−2, and the period with the lowest primary productivity was between July and September, with a maximum of 1484 mg C m−2. In 2022, the months with the highest primary productivity were between July and September, with a maximum of 2797 mg C m−2, and the minimum was between January and March. Finally, in 2023, the maximum was between January and March, which peaked at 1831 mg C m−2, while the minimum was between April and June, with a maximum of 1185 mg C m−2 (Figure 7).
Regarding SST, it was observed that 2023 was warmer than previous years. The coldest months were July to September 2021 and July to September 2022, whereas in 2023, it was considerably warmer across the years, reaching a peak of 29 °C. In 2020, sea surface temperatures (SST) peaked from April to June at 29 °C, with the lowest recorded in July to September at 21 °C. In 2021, the highest temperature occurred between January and March, reaching 27 °C, while the lowest was between July and September, ranging from 25 °C to 17 °C. Similarly, in 2022, the peak was from January to March at 27 °C, and the lowest temperature occurred between July and September, ranging from 25 °C to 15 °C. Notably, temperatures soared in 2023, peaking at 29 °C between January and March and April to June, with the lowest temperature observed from July to September at 22 °C, surpassing any values recorded in the previous four years (Figure 8).
Additionally, the ONI data indicated that during the period from July to August 2023, the ONI was at a moderate level. However, from September to November 2023, the ONI was strong, reaching very strong levels in November. For the remaining years, the ONI showed La Niña conditions, except for 2020, where the early months exhibited weak El Niño conditions (Figure 9).

4. Discussion

This study aimed to elucidate blue whales’ poorly understood movement patterns in the Galapagos archipelago and beyond. It is the first to employ satellite tagging of blue whales within the Galapagos. By integrating data from these tags with the remote sensing of productivity proxies, we sought to understand the influence of these factors on their migratory and foraging behavior. It was previously believed that blue whales use the Galapagos during the cooler seasons (austral winter and spring) for breeding and return to their southern feeding grounds off Chile and Peru during the austral summer [31,57]. However, occasional sightings of blue whales in the Galapagos during the warmer season indicated a year-round presence [36,58]. Our findings indicate that most tagged whales remained near the islands for the duration of the transmission period. However, due to the temporal constraints of the transmission data, we could not definitively confirm continuous year-round residency. Nevertheless, our data underscore the significance of the Galapagos archipelago as a critical foraging area for these blue whales.
The Galapagos Islands are renowned for their marine mammal diversity, particularly cetaceans, with 23 species documented, some of which are residents [59]. Historically, the Galapagos archipelago was a major hotspot for whaling in the late 18th and 19th centuries [31,50,51,52,53,54,55,56,57,58], further emphasizing its longstanding significance as a breeding and foraging ground for resident and migratory whales. The region’s unique hydrographic conditions create a transition zone between tropical and subtropical waters, characterized by strong local and seasonal upwelling [60]. This increases primary productivity, particularly in the western part [60,61], leading to higher cetacean densities in this area [62]. Our results corroborate this, showing that whales predominantly use the western part of the archipelago, yet with the highest occurrences around Isabela Island rather than the previously described Canal Bolivar (Figure 1) [36,58]. This information is crucial for managing tourist operations to minimize disturbances to the animals’ feeding and calving behaviors and to mitigate the risk of ship strikes.
While most individuals remained close to the Galapagos, two foraged in the Ecuador EEZ and one (#178968) off Peru, indicating linkages to the SEP, as previously shown [23,29,30,38,39]. However, recent evidence from Guzman and Estevez [39] indicates that the Galapagos may also serve as a stepping stone, connecting northern and southern Pacific blue whale populations.
Overall, blue whale migratory routes have been shown to align with the trajectories of dense krill aggregations [54,55,56,63,64]. Long-term memory likely facilitates the annual return of blue whales to foraging grounds, where food availability remains consistently high over extended periods [63]. Submarine geomorphic features such as ridges, canyons, seamounts, and oceanic islands may also serve as navigation cues for baleen whales [65,66,67,68]. These features influence hydrographic conditions, resulting in local upwelling and changes in nutrient and SST (e.g., El Niño) levels supporting substantial krill populations [28,55,56,69,70]. Moreover, they could serve as potential navigational landmarks during long-distance migrations, though this aspect remains inadequately understood [67,71,72].
We observed associations between geomorphic features and foraging behaviors, including migrations along continental shelf edges and ridges, i.e., the Carnegie and Nazca ridges, previously identified as critical migratory routes for blue whales; the Salas y Gómez and Nazca ridges are recognized as regular migratory pathways for the Chilean blue whale en route to the Galapagos Islands for feeding [23,73,74,75]. The Carnegie Ridge has been recently declared an Important Marine Mammal Area of 459,869 km2 (https://www.marinemammalhabitat.org/factsheets/carnegie-ridge-galapagos-to-mainland-imma/ [accessed on 20 June 2024]). Whales in our study utilized the Nazca and Carnegie ridges for feeding, likely due to the high productivity in these regions. Northern Peru benefits from the nutrient influx driven by the northern Humboldt Current system [76] and the Nazca Ridge exhibits increased biological productivity [77]. Meanwhile, Carnegie Ridge, a transition area between the Humboldt Current and the eastern Pacific equatorial front, exhibits high surface productivity due to divergent equatorial upwelling and the advection of cool, nutrient-rich waters [78].
Blue whales show a distinct preference for feeding in various bathymetric zones, notably favoring deeper waters. This depth preference is likely a reflection of the role bathymetric features play in concentrating planktonic organisms, which attract blue whales to these highly productive areas [79,80]. Nevertheless, this does not necessarily mean that the whales are feeding at greater depths directly; rather, it suggests an association with regions where bathymetric conditions enhance overall productivity. Thus, while blue whale feeding behavior is linked to deeper waters, it is the increased productivity facilitated by these bathymetric features that likely drives their foraging preferences.
Our study established a link between environmental correlates—specifically sea surface temperature (SST), chlorophyll-a (Chl-a) concentrations, and productivity—and the movement behavior of blue whales. Foraging activity was notably more prevalent in regions with lower SST and higher Chl-a concentrations and productivity, indicative of high prey densities (e.g., [53,54,55,81]). This correlation suggests a feedback loop, where productive foraging areas also exhibit high whale densities, reinforcing the importance of these regions as critical habitats for blue whales. This relationship is important as it implies that environmental correlates can be utilized to predict areas of probable whale occurrence, thereby aiding in identifying critical habitats essential for managing and conserving endangered species [82].
Blue whales also demonstrate the ability to adapt temporally [83,84] and spatially [64] to their prey’s patchy and ephemeral nature. For example, Szesciorka et al. [83] discovered that seasonal variations in SST in the California Current Ecosystem led to blue whales arriving earlier for feeding. Cooler temperatures were associated with higher krill biomass in the following season, demonstrating the whales’ ability to adjust their migratory timing in response to interannual environmental changes. SST, therefore, acts as a migratory cue influencing their behavior [53,54,55]. Understanding these patterns is key for conservation, particularly in timing the whales’ arrival at feeding and breeding grounds, which can inform temporal conservation measures [83]. Conducted during a strong ENSO year (2023), our study identified substantial changes in SST and surface primary production. Despite the lack of discernible behavioral differences—likely due to the limited sample size of only two tagged whales in 2023—the environmental perturbations driven by the ENSO could significantly impact resource availability. Conversely, the limited number of specimens tagged, despite intensified efforts this year, suggests potential changes in whale presence or behavior during significant ENSO events. As more frequent and extreme ENSO events are predicted (e.g., [85]), these changes can impact blue whale behavior, habitat utilization, and reproductive success [83,86].

5. Conclusions

Our findings highlight the importance of understanding blue whale migratory and foraging patterns to inform conservation strategies. The alignment of blue whale migratory routes with high-productivity areas underscores the necessity of protecting key foraging grounds that provide consistent food resources. As environmental changes, such as ENSO events alter chlorophyll, primary productivity, and SST, blue whales may have to adapt their migratory and foraging behaviors. This adaptability suggests a need for dynamic conservation measures that can respond to shifting environmental conditions.
Additionally, heavy ship traffic along migratory routes, particularly the presence of tourist vessels in areas of high whale density like Isla Isabela in the Galapagos [87], may pose a significant threat to blue whales (see also [88]). Implementing measures to mitigate ship strikes, such as limiting the number of boats or their proximity to whales, altering shipping lanes, and enforcing speed restrictions in critical habitats, is essential to reduce mortality risks (e.g., [89,90]). Conservation efforts must also account for the impacts of climate change, which could further affect the availability and distribution of prey, necessitating a comprehensive approach to ensure the long-term survival of blue whale populations. By integrating environmental correlates into conservation planning, we can better predict whale occurrence and protect essential habitats [33,82]. Continued research and monitoring are vital to adapting conservation strategies to the dynamic nature of marine ecosystems, ultimately supporting the preservation of these magnificent ocean giants.

Author Contributions

Conceptualization, H.M.G.; methodology, H.M.G.; formal analysis, R.M.E.; investigation, H.M.G., R.M.E. and S.K.; data curation, R.M.E.; writing—original draft preparation, H.M.G., R.M.E. and S.K.; writing—review and editing, H.M.G., R.M.E. and S.K.; project administration, H.M.G.; funding acquisition, H.M.G. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Smithsonian Tropical Research Institute, the Isla Secas Foundation (No. 505394, 27 September 2023), donations from the Anne Page Chiapella Family, and the Sistema Nacional de Investigadores (SNI) from SENACYT, Panama.

Institutional Review Board Statement

The study was conducted in accordance with the Smithsonian Institution’s general guidelines. The Smithsonian Tropical Research Institute Animal and Care Committee reviewed and approved the animal study (No. 2017-0915-2019, 16 June 2016; No. 2020-0305-2023, 5 March 2020; SI-23043, 30 August 2023).

Informed Consent Statement

Not applicable.

Data Availability Statement

The data supporting this study’s findings are available from the first author [HMG] upon reasonable request due to privacy restrictions.

Acknowledgments

The authors thank the Government of Ecuador and the Galapagos Park Service, particularly Jenifer Suarez, for providing the research permits and institutional support. We gratefully acknowledge Captain Yuri Revelo’s help maneuvering the boat while tagging and the crew of the FV Yualka II for invaluable logistical and field support. We also thank Daniela Alarcon and Fernando Rivera for institutional and field assistance. We thank the three anonymous reviewers who provided comments and insights to improve the manuscript.

Conflicts of Interest

The authors declare no conflicts of interest. The funders had no role in the study’s design, data collection, analysis, interpretation, manuscript writing, or decision to publish the results.

References

  1. Jackson, J. Ecological extinction and evolution in the brave new ocean. Proc. Natl. Acad. Sci. USA 2008, 105 (Suppl. S1), 11458–11465. [Google Scholar] [CrossRef]
  2. O’Hara, C.; Frazier, M.; Halpern, B. At-risk marine biodiversity faces extensive, expanding, and intensifying human impacts. Science 2021, 372, 84–87. [Google Scholar] [CrossRef] [PubMed]
  3. Selig, E.; Turner, W.; Troëng, S.; Wallace, B.; Halpern, B.; Kaschner, K.; Lascelles, B.; Carpenter, K.; Mittermeier, R. Global priorities for marine biodiversity conservation. PLoS ONE 2014, 9, e82898. [Google Scholar] [CrossRef]
  4. Sandifer, P.; Sutton-Grier, A. Connecting stressors, ocean ecosystem services, and human health. Nat. Resour. Forum 2014, 38, 157–167. [Google Scholar] [CrossRef]
  5. Chami, R.; Cosimano, T.; Fullenkamp, C.; Oztosun, S. Nature’s solution to climate change. Financ. Dev. 2019, 56, 34–38. [Google Scholar]
  6. Menegotto, A.; Rangel, T. Mapping knowledge gaps in marine diversity reveals a latitudinal gradient of missing species richness. Nat. Commun. 2018, 9, 4713. [Google Scholar] [CrossRef]
  7. Attard, C.; Beheregaray, L.; Möller, L. Towards population-level conservation in the critically endangered Antarctic blue whale: The number and distribution of their populations. Sci. Rep. 2016, 6, 22291. [Google Scholar] [CrossRef]
  8. Cooke, J. Balaenoptera musculus (Errata Version Published in 2019). The IUCN Red List of Threatened Species. 2018. Available online: https://dx.doi.org/10.2305/IUCN.UK.2018-2.RLTS.T2477A156923585.en (accessed on 15 February 2019).
  9. Branch, T.A.; Matsuoka, K.; Miyashita, T. Evidence for increases in Antarctic blue whales based on Bayesian modelling. Mar. Mammal Sci. 2004, 20, 726–754. [Google Scholar] [CrossRef]
  10. Branch, T.; Stafford, K.; Palacios, D.; Allison, C.; Bannister, J.; Burton, C.; Cabrera, E.; Carlson, C.; Galletti Vernazzani, B.; Gill, P.; et al. Past and present distribution, densities and movements of blue whales Balaenoptera musculus in the Southern Hemisphere and northern Indian Ocean. Mammal Rev. 2007, 37, 116–175. [Google Scholar] [CrossRef]
  11. National Marine Fisheries Service. Draft Recovery Plan for the Blue Whale (Balaenoptera musculus)—Revision; National Marine Fisheries Service, Office of Protected Resources: Silver Spring, MD, USA, 2018.
  12. Reeves, R.; Clapham, P.; Brownell, R.; Silber, G. Recovery Plan for the Blue Whale (Balaenoptera musculus); Office of Protected Resources, National Marine Fisheries Service: Silver Spring, MD, USA, 1998; p. 42. [Google Scholar]
  13. Calambokidis, J.; Barlow, J. Abundance of blue and humpback whales in the eastern North Pacific estimated by capture-recapture and line-transect methods. Mar. Mammal Sci. 2004, 20, 63–85. [Google Scholar] [CrossRef]
  14. LeDuc, R.G.; Archer, E.; Lang, A.; Martien, K.; Hancock-Hanser, B.; Torres-Florez, J.; Hucke-Gaete, R.; Rosenbaum, H.; Van Waerebeek, K.; Brownell, R.; et al. Genetic variation in blue whales in the Eastern Pacific: Implication for taxonomy and use of common wintering grounds. Mol. Ecol. 2017, 26, 740–751. [Google Scholar] [CrossRef] [PubMed]
  15. Ichihara, T. The pygmy blue whale, Balaenoptera musculus brevicauda, a new subspecies from the Antarctic. In Whales, Dolphins, and Porpoises; Norris, K.S., Ed.; University of California Press: Berkeley, CA, USA, 1966; pp. 79–111. [Google Scholar]
  16. Rice, D. Marine Mammals of the World: Systematics and Distribution; The Society for Marine Mammalogy: Lawrence, KS, USA, 1998. [Google Scholar]
  17. Attard, C.; Beheregaray, L.; Jenner, K.; Gill, P.; Jenner, M.; Morrice, M.; Peter, R.; Möller, L. Low genetic diversity in pygmy blue whales is due to climate-induced diversification rather than anthropogenic impacts. Biol. Lett. 2015, 11, 20141037. [Google Scholar] [CrossRef]
  18. Anderson, R.; Branch, T.; Alagiyawadu, A.; Baldwin, R.; Marsac, F. Seasonal distribution, movements and taxonomic status of blue whales (Balaenoptera musculus) in the northern Indian Ocean. J. Cetacean Res. Manag. 2012, 12, 203–218. [Google Scholar] [CrossRef]
  19. International Whaling Commission. Report of the Scientific Committee. Available online: https://archive.iwc.int/pages/view.php?ref=19277&k= (accessed on 20 August 2021).
  20. Pastene, L.; Acevedo, J.; Branch, T. Morphometric analysis of Chilean blue whales and implications for their taxonomy. Mar. Mammal Sci. 2020, 36, 116–135. [Google Scholar] [CrossRef]
  21. Gambell, R. The Blue Whale. Biologist 1979, 26, 209–215. [Google Scholar]
  22. Donovan, G. A review of IWC stock boundaries. Rep. Int. Whal. Commn 1991, 13, 39–68. [Google Scholar]
  23. Torres-Florez, J.; Hucke-Gaete, R.; LeDuc, R.; Lang, A.; Taylor, B.; Pimper, L.; Bedriñana-Romano, L.; Rosenbaum, H.; Figueroa, C. Blue whale population structure along the eastern South Pacific Ocean: Evidence of more than one population. Mol. Ecol. 2014, 29, 5998–6010. [Google Scholar] [CrossRef]
  24. McDonald, M.; Mesnick, S.; Hildebrand, J. Biogeographic characterisation of blue whale song worldwide: Using song to identify populations. J. Cetacean Res. Manag. 2006, 8, 55–65. [Google Scholar] [CrossRef]
  25. Buchan, S.; Hucke-Gaete, R.; Rendell, L.; Stafford, K. A new song recorded from blue whales in the Corcovado Gulf, Southern Chile, and an acoustic link to the Eastern Tropical Pacific. Endanger. Spec. Res. 2014, 23, 241–252. [Google Scholar] [CrossRef]
  26. Barlow, D.; Klinck, H.; Ponirakis, D.; Holt Colberg, M.; Torres, L. Temporal occurrence of three blue whale populations in New Zealand waters from passive acoustic monitoring. J. Mammal. 2023, 104, 29–38. [Google Scholar] [CrossRef]
  27. Cerchio, S.; Willson, A.; Leroy, E.; Muirhead, C.; Al Harthi, S.; Baldwin, R.; Cholewiak, D.; Collins, T.; Minton, G.; Rasoloarijao, T.; et al. A new blue whale song-type described for the Arabian Sea and Western Indian Ocean. Endanger. Spec. Res. 2020, 43, 495–515. [Google Scholar] [CrossRef]
  28. Croll, D.; Marinovic, B.; Benson, S.; Chavez, F.; Black, N.; Tershy, B. From wind to whales: Trophic links in an upwelling ecosystem. Mar. Ecol. Prog. Ser. 2005, 289, 117–130. [Google Scholar] [CrossRef]
  29. Palacios, D. Blue whale (Balaenoptera musculus) occurrence off the Galapagos Islands, 1978–1995. J. Cetacean Res. Manag. 1999, 1, 41–51. [Google Scholar] [CrossRef]
  30. Kawamura, A. A review of food of balaenopterid whales. Sci. Rep. Whales Res. Inst. 1980, 32, 155–170. [Google Scholar]
  31. Reilly, S.B.; Thayer, V.G. Blue whale (Balaenoptera musculus) distribution in the Eastern Tropical Pacific. Mar. Mammal Sci. 1990, 6, 265–277. [Google Scholar] [CrossRef]
  32. Findlay, K.; Pitman, R.; Tsurui, T.; Sakai, K.; Ensor, P.; Iwakami, H.; Ljungblad, D.; Shimada, H.; Thiele, D.; Van Waerebeek, K.; et al. 1997/1998 IWC-Southern Ocean Whale and Ecosystem Research (IWC-SOWER) Blue Whale Cruise, Chile; Paper SC/50/Rep2 presented to the IWC Scientific Committee April 1998 (unpublished); International Whaling Commission: Muscat, Oman, 1998. [Google Scholar]
  33. Hucke-Gaete, R.; Bedrinana-Romano, L.; Viddi, F.; Ruiz, J.; Torres-Florez, J.; Zerbini, A. From Chilean Patagonia to Galapagos, Ecuador: Novel insights on blue whale migratory pathways along the Eastern South Pacific. PeerJ 2018, 6, e4695. [Google Scholar] [CrossRef]
  34. Sirovic, A.; Hildebrand, J.; Wiggins, S.; McDonald, M.; Moore, S.; Thiele, D. Seasonality of blue and fin whale calls west of the Antarctic Peninsula. Deep Sea Res. II 2004, 51, 2327–2344. [Google Scholar] [CrossRef]
  35. Samaran, F.; Adam, O.; Guinet, C. Discovery of a mid-latitude sympatric area for two Southern Hemisphere blue whale subspecies. Endanger. Spec. Res. 2010, 12, 157–165. [Google Scholar] [CrossRef]
  36. Denkinger, J.; Douglas, A.; Biggs, D.; Sears, R.; Narvaez, M.; Alarcon, D. Year-round presence of northern and southern hemisphere blue whales (Balaenoptera musculus) at the Galapagos Archipelago. J. Cetacean Res. Manag. 2023, 24, 63–76. [Google Scholar] [CrossRef]
  37. Stafford, K.; Bohnenstiehl, D.; Tolstoy, M.; Chapp, E.; Mellinger, D.; Moore, S. Antarctic-type blue whale calls recorded at low latitudes in the Indian and eastern Pacific Oceans. Deep Sea Res. I 2004, 51, 1337–1346. [Google Scholar] [CrossRef]
  38. Stafford, K.; Nieukirk, S.; Fox, C. An acoustic link between blue whales in the eastern tropical Pacific and the northeast Pacific. Mar. Mammal Sci. 1999, 15, 1258–1268. [Google Scholar] [CrossRef]
  39. Guzman, H.M.; Estévez, R.M. Connectivity between Northeast and Southeast Pacific blue whale populations in the Galapagos Archipelago. Mar. Mammal Sci. 2024; in press. [Google Scholar]
  40. Alarcón-Ruales, D.; Denkinger, J.; Zurita-Arthos, L.; Herrera, S.; Díaz-Pazmiño, S.; Espinoza, E.; Muñoz Pérez, J.P.; Holmes, B.J.; Townsend, K.A. Cetaceans of the Galapagos Archipelago: Species in Constant Change and the Importance of a Standardized and Long-Term Citizen Science Program. In Island Ecosystems: Challenges to Sustainability; Springer International Publishing: Cham, Switzerland, 2023; pp. 335–355. [Google Scholar]
  41. Guzman, H.M.; Gómez, C.; Guevara, C.; Kleivane, L. Potential vessel collisions with Southern Hemisphere humpback whales wintering off Pacific Panama. Mar. Mammal Sci. 2013, 29, 629–642. [Google Scholar] [CrossRef]
  42. Kleivane, L.; Kvadsheim, P.H.; Bocconcelli, A.; Øien, N.; Miller, P. Equipment to tag, track and collect biopsies from whales and dolphins: The ARTS, DFHorten and LKDart systems. Anim. Biotelemetry 2022, 10, 32. [Google Scholar] [CrossRef]
  43. Vincent, C.; McConnell, B.J.; Ridoux, V.; Fedak, M. Assessment of Argos location accuracy from satellite tags deployed on captive gray seals. Mar. Mammal Sci. 2002, 18, 156–166. [Google Scholar] [CrossRef]
  44. Guzman, H.M.; Félix, F. Movements and habitat use by Southeast Pacific humpback whales (Megaptera novaeangliae) satellite tracked at two breeding sites. Aquat. Mamm. 2017, 43, 139. [Google Scholar] [CrossRef]
  45. Douglas, D.C.; Weinzierl, R.; Davidson, S.C.; Kays, R.; Wikelski, M.; Bohrer, G. Moderating Argos location errors in animal tracking data. Methods Ecol. Evol. 2012, 3, 999–1007. [Google Scholar] [CrossRef]
  46. Hucke-Gaete, R.; Osman, L.; Moreno, C.; Findlay, K.; Ljungblad, D. Discovery of a blue whale feeding and nursing ground in southern Chile. Proc. R. Soc. Lond. B 2004, 271 (Suppl. S4), S1. [Google Scholar] [CrossRef]
  47. Jonsen, I.; McMahon, C.; Patterson, T.; Auger-Méthé, M.; Harcourt, R.; Hindell, M.; Bestley, S. Movement responses to environment: Fast inference of variation among southern elephant seals with a mixed effects model. Ecology 2019, 100, e02566. [Google Scholar] [CrossRef]
  48. Jonsen, I.; Grecian, W.; Phillips, L.; Carroll, G.; McMahon, C.; Harcourt, R.; Hindell, M.; Patterson, T. aniMotum, an R package for animal movement data: Rapid quality control, behavioral estimation and simulation. Methods Ecol. Evol. 2023, 17, 806–816. [Google Scholar] [CrossRef]
  49. R Core Team. R: A Language and Environment for Statistical Computing; R Foundation for Statistical Computing: Vienna, Austria, 2024; Available online: www.R-project.org/ (accessed on 1 February 2024).
  50. Michelot, T.; Langrock, R.; Patterson, T. moveHMM: An R package for the statistical modelling of animal movement data using hidden Markov models. Methods Ecol. Evol. 2016, 7, 1308–1315. [Google Scholar] [CrossRef]
  51. Mendelssohn, R. Xtractomatic: Accessing Environmental Data from ERD’s ERDDAP Server, R Package Version 3.4.2. 2018. Available online: https://cran.r-project.org/src/contrib/Archive/xtractomatic/ (accessed on 1 February 2024).
  52. Mayer, L.; Jakobsson, M.; Allen, G.; Dorschel, B.; Falconer, R.; Ferrini, V.; Lamarche, G.; Snaith, H.; Weatherall, P. The nippon foundation—GEBCO seabed 2030 project: The quest to see the world’s oceans completely mapped by 2030. Geosciences 2018, 8, 63. [Google Scholar] [CrossRef]
  53. Irvine, L.M.; Mate, B.R.; Winsor, M.H.; Palacios, D.M.; Bograd, S.J.; Costa, D.P.; Bailey, H. Spatial and temporal occurrence of blue whales off the US West Coast, with implications for management. PLoS ONE 2014, 9, e102959. [Google Scholar] [CrossRef] [PubMed]
  54. Nickels, C.F.; Sala, L.M.; Ohman, M.D. The euphausiid prey field for blue whales around a steep bathymetric feature in the southern California current system. Limnol. Oceanogr. 2019, 64, 390–405. [Google Scholar] [CrossRef]
  55. Benson, S.R.; Croll, D.A.; Marinovic, B.B.; Chavez, F.P.; Harvey, J.T. Changes in the cetacean assemblage of a coastal upwelling ecosystem during El Niño 1997–98 and La Niña 1999. Progr. Oceanogr. 2002, 54, 279–291. [Google Scholar] [CrossRef]
  56. Torres, L.G.; Barlow, D.R.; Hodge, K.; Klinck, H.; Steel, D.; Baker, C.S.; Chandler, T.; Gill, P.; Ogle, M.; Lilley, C.; et al. New Zealand blue whales: Recent findings and research progress. J. Cetacean Res. Manag. 2017, 1–22. [Google Scholar]
  57. Palacios, D.M. Marine Mammal Research in the Galápagos Islands: The 1993–1994 Odyssey Expedition; Galápagos National Park Service and Charles Darwin Research Station: Puerto Ayora, Galápagos, Ecuador, 1999. [Google Scholar]
  58. Denkinger, J.; Oña, J.; Alarcón, D.; Merlen, G.; Salazar, S.; Palacios, D.M. From whaling to whale watching: Cetacean presence and species diversity in the Galápagos Marine Reserve. In Science and Conservation in the Galapagos Islands: Frameworks & Perspectives; Harpp, K.S., Ed.; Springer: New York, NY, USA, 2013; pp. 217–235. [Google Scholar]
  59. Palacios, D.M.; Cantor, M. Priorities for ecological research on cetaceans in the Galápagos Islands. Front. Mar. Sci. 2023, 10, 1084057. [Google Scholar] [CrossRef]
  60. Forryan, A.; Naveira Garabato, A.C.; Vic, C.; Nurser, A.G.; Hearn, A.R. Galápagos upwelling driven by localized wind–front interactions. Sci. Rep. 2021, 11, 1277. [Google Scholar] [CrossRef]
  61. Palacios, D.M. Seasonal patterns of sea-surface temperature and ocean color around the Galapagos: Regional and local influences. Deep-Sea Res. II 2004, 51, 43–57. [Google Scholar] [CrossRef]
  62. Alava, J.J. Carbon productivity and flux in the marine ecosystems of the Galapagos Marine Reserve based on cetacean abundances and trophic indices. Rev. Biol. Mar. Oceanogr. 2009, 44, 109–122. [Google Scholar] [CrossRef]
  63. Abrahms, B.; Hazen, E.L.; Aikens, E.O.; Savoca, M.S.; Goldbogen, J.A.; Bograd, S.J.; Mate, B.R. Memory and resource tracking drive blue whale migrations. Proc. Natl. Acad. Sci. USA 2019, 116, 5582–5587. [Google Scholar] [CrossRef]
  64. Ryan, J.P.; Benoit-Bird, K.J.; Oestreich, W.K.; Leary, P.; Smith, K.B.; Waluk, C.M.; Goldbogen, J.A. Oceanic giants dance to atmospheric rhythms: Ephemeral wind-driven resource tracking by blue whales. Ecol. Lett. 2022, 25, 2435–2447. [Google Scholar] [CrossRef]
  65. Rennie, S.; Hanson, C.E.; McCauley, R.D.; Pattiaratchi, C.; Burton, C.; Bannister, J.; Jenner, C.; Jenner, M.N. Physical properties and processes in the Perth Canyon, Western Australia: Links to water column production and seasonal pygmy blue whale abundance. J. Mar. Syst. 2009, 77, 21–44. [Google Scholar] [CrossRef]
  66. Lesage, V.; Gavrilchuk, K.; Andrews, R.D.; Sears, R. Foraging areas, migratory movements and winter destinations of blue whales from the western North Atlantic. Endanger. Spec. Res. 2017, 34, 27–43. [Google Scholar] [CrossRef]
  67. Prieto, R.; Tobeña, M.; Silva, M.A. Habitat preferences of baleen whales in a mid-latitude habitat. Deep-Sea Res. II 2017, 141, 155–167. [Google Scholar] [CrossRef]
  68. Derville, S.; Torres, L.G.; Zerbini, A.N.; Oremus, M.; Garrigue, C. Horizontal and vertical movements of humpback whales inform the use of critical pelagic habitats in the western South Pacific. Sci. Rep. 2020, 10, 4871. [Google Scholar] [CrossRef] [PubMed]
  69. Genin, A. Bio-physical coupling in the formation of zooplankton and fish aggregations over abrupt topographies. J. Mar. Syst. 2004, 50, 3–20. [Google Scholar] [CrossRef]
  70. Santora, J.A.; Zeno, R.; Dorman, J.G.; Sydeman, W.J. Submarine canyons represent an essential habitat network for krill hotspots in a large marine ecosystem. Sci. Rep. 2018, 8, 7579. [Google Scholar] [CrossRef]
  71. Luschi, P. Long-distance animal migrations in the oceanic environment: Orientation and navigation correlates. Int. Schol. Res. Notices 2013, 2013, 631839. [Google Scholar] [CrossRef]
  72. Thouless, C. Where the Whales Go: The Migration Routes of Humpbacks in the South West Atlantic. Master’s Thesis, The University of California, San Diego, CA, USA, 2021. Available online: https://escholarship.org/uc/item/1693m1b5 (accessed on 15 June 2024).
  73. Hucke-Gaete, R.; Lobo, A.; Yancovic-Pakarati, S.; Flores, M. Mamíferos marinos de la isla de pascua (Rapa Nui) e isla Salas y Gómez (Motu Motiro Hiva), Chile: Una revisión y nuevos registros. Lat. Am. J. Aquat. Res. 2014, 42, 743–751. [Google Scholar] [CrossRef]
  74. Buchan, S.; Hucke-Gaete, R.; Stafford, K.M.; Clark, C.W. Occasional acoustic presence of Antarctic blue whales on a feeding ground in southern Chile. Mar. Mammal Sci. 2017, 34, 440–458. [Google Scholar] [CrossRef]
  75. Convention on Biological Diversity (CBD). Ecologically or Biologically Significant Areas (EBSAs). 2017. Available online: https://chm.cbd.int/database/record?documentID=204100 (accessed on 10 June 2024).
  76. Massing, J.C.; Schukat, A.; Auel, H.; Auch, D.; Kittu, L.; Pinedo Arteaga, E.L.; Hagen, W. Toward a solution of the “Peruvian Puzzle”: Pelagic food-web structure and trophic interactions in the northern Humboldt current upwelling system off Peru. Front. Mar. Sci. 2022, 8, 759603. [Google Scholar] [CrossRef]
  77. Daneri, G.; Dellarossa, V.; Quiñones, R.; Jacob, B.; Montero, P.; Ulloa, O. Primary production and community respiration in the Humboldt Current System off Chile and associated oceanic areas. Mar. Ecol. Prog. Ser. 2000, 197, 41–49. [Google Scholar] [CrossRef]
  78. Faul, K.L.; Ravelo, A.C.; Delaney, M.L. Reconstructions of upwelling, productivity, and photic zone depth in the eastern equatorial Pacific Ocean using planktonic foraminiferal stable isotopes and abundances. J. Foraminifer. Res. 2000, 30, 110–125. [Google Scholar] [CrossRef]
  79. Buchan, S.J.; Quiñones, R.A. First insights into the oceanographic characteristics of a blue whale feeding ground in northern Patagonia, Chile. Mar. Ecol. Prog. Ser. 2016, 554, 183–199. [Google Scholar] [CrossRef]
  80. Buchan, S.J.; Pérez-Santos, I.; Narváez, D.; Castro, L.; Stafford, K.M.; Baumgartner, M.F.; Valle-Levinson, A.; Montero, P.; Gutiérrez, L.; Rojas, C.; et al. Intraseasonal variation in southeast Pacific blue whale acoustic presence, zooplankton backscatter, and oceanographic variables on a feeding ground in Northern Chilean Patagonia. Progr. Oceanogr. 2021, 199, 102709. [Google Scholar] [CrossRef]
  81. Hazen, E.L.; Friedlaender, A.S.; Goldbogen, J.A. Blue whales (Balaenoptera musculus) optimize foraging efficiency by balancing oxygen use and energy gain as a function of prey density. Sci. Adv. 2015, 1, e1500469. [Google Scholar] [CrossRef] [PubMed]
  82. Palacios, D.M.; Bailey, H.; Becker, E.A.; Bograd, S.J.; DeAngelis, M.L.; Forney, K.A.; Mate, B.R. Ecological correlates of blue whale movement behavior and its predictability in the California Current Ecosystem during the summer-fall feeding season. Mov. Ecol. 2019, 7, 26. [Google Scholar] [CrossRef]
  83. Szesciorka, A.R.; Ballance, L.T.; Širović, A.; Rice, A.; Ohman, M.D.; Hildebrand, J.A.; Franks, P.J.S. Timing is everything: Drivers of interannual variability in blue whale migration. Sci. Rep. 2020, 10, 7710. [Google Scholar] [CrossRef]
  84. Oestreich, W.K.; Abrahms, B.; McKenna, M.F.; Goldbogen, J.A.; Crowder, L.B.; Ryan, J.P. Acoustic signature reveals blue whales tune life-history transitions to oceanographic conditions. Funct. Ecol. 2022, 36, 882–895. [Google Scholar] [CrossRef]
  85. Lee, T.; McPhaden, M.J. Increasing intensity of El Niño in the central-equatorial Pacific. Geophys. Res. Lett. 2010, 37, L14603. [Google Scholar] [CrossRef]
  86. Truong, G.; Rogers, T.L. La Niña conditions influence interannual call detections of pygmy blue whales in the eastern Indian Ocean. Front. Mar. Sci. 2023, 9, 850162. [Google Scholar] [CrossRef]
  87. Denkinger, J.; Parra, M.; Muñoz, J.P.; Carrasco, C.; Murillo, J.C.; Espinosa, E.; Koch, V. Are boat strikes a threat to sea turtles in the Galapagos Marine Reserve? Ocean Coast. Manag. 2013, 80, 29–35. [Google Scholar] [CrossRef]
  88. Ransome, N.; Loneragan, N.R.; Medrano-González, L.; Félix, F.; Smith, J.N. Vessel strikes of large whales in the eastern tropical Pacific: A case study of regional underreporting. Front. Mar. Sci. 2021, 8, 675245. [Google Scholar] [CrossRef]
  89. Sitar, A.; McCauley, L.J.; Wright, A.J.; Peters-Burton, E.; Rockwood, L.; Parsons, E.C.M. Boat operators in Bocas del Toro, Panama display low levels of compliance with national whale-watching regulations. Mar. Policy 2016, 68, 221–228. [Google Scholar] [CrossRef]
  90. Guzman, H.M.; Hinojosa, N.; Kaiser, S. Ship’s compliance with a traffic separation scheme and speed limit in the Gulf of Panama and implications for the risk to humpback whales. Mar. Policy 2020, 120, 104113. [Google Scholar] [CrossRef]
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Figure 1. Kernel density of high-, medium-, and low-use areas used by blue whales tagged in the Galapagos Islands.
Figure 1. Kernel density of high-, medium-, and low-use areas used by blue whales tagged in the Galapagos Islands.
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Figure 2. Blue whale migration using the state–space model, tagged in 2021, 2022, and 2023. Lower gamma_t values (ranging from orange to purple) highlight regions where the whale is likely engaged in area-restricted search behavior, while higher gamma_t values (shifting from light orange to yellow) indicate areas where whales exhibit directed, rapid movements. Numbers indicate the whale’s identity.
Figure 2. Blue whale migration using the state–space model, tagged in 2021, 2022, and 2023. Lower gamma_t values (ranging from orange to purple) highlight regions where the whale is likely engaged in area-restricted search behavior, while higher gamma_t values (shifting from light orange to yellow) indicate areas where whales exhibit directed, rapid movements. Numbers indicate the whale’s identity.
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Figure 3. Migration (blue dots) and foraging (yellow dots) states of blue whales tagged in the Galapagos archipelago inferred by HMM modeling over GEBCO bathymetry [50].
Figure 3. Migration (blue dots) and foraging (yellow dots) states of blue whales tagged in the Galapagos archipelago inferred by HMM modeling over GEBCO bathymetry [50].
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Figure 4. Long-term probabilities of blue whales at different values of the covariates. Chlorophyll (A), productivity (B), and sea surface temperature (C) in each behavioral state, foraging (orange: state 1) and migrating (blue: state 2), with alpha = 0.9 confidence intervals.
Figure 4. Long-term probabilities of blue whales at different values of the covariates. Chlorophyll (A), productivity (B), and sea surface temperature (C) in each behavioral state, foraging (orange: state 1) and migrating (blue: state 2), with alpha = 0.9 confidence intervals.
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Figure 5. Environmental conditions during migration and foraging states modeled by a hidden Markov model. Blue whales preferred to forage when chlorophyll and primary productivity levels were higher and when sea surface temperature was lower. Stars indicate a significant difference.
Figure 5. Environmental conditions during migration and foraging states modeled by a hidden Markov model. Blue whales preferred to forage when chlorophyll and primary productivity levels were higher and when sea surface temperature was lower. Stars indicate a significant difference.
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Figure 6. Difference in quarterly chlorophyll concentration (mg m−3) per year (2020, 2021, 2022, and 2023).
Figure 6. Difference in quarterly chlorophyll concentration (mg m−3) per year (2020, 2021, 2022, and 2023).
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Figure 7. Difference in quarterly primary productivity (mg C m−2) per year (2020, 2021, 2022, and 2023).
Figure 7. Difference in quarterly primary productivity (mg C m−2) per year (2020, 2021, 2022, and 2023).
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Figure 8. Difference in sea surface temperature (°C) per year (2020, 2021, 2022, and 2023).
Figure 8. Difference in sea surface temperature (°C) per year (2020, 2021, 2022, and 2023).
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Figure 9. Oceanic Niño Index (ONI) from 2020 to 2023.
Figure 9. Oceanic Niño Index (ONI) from 2020 to 2023.
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Table 1. Summary of tracked blue whales tagged off the Galapagos Islands and their time within Ecuador’s economic exclusive zone (EEZ).
Table 1. Summary of tracked blue whales tagged off the Galapagos Islands and their time within Ecuador’s economic exclusive zone (EEZ).
IdTagging Date
(mm-dd-yyyy)		Last Date
(mm-dd-yyyy)		Transmissions
(Days)		Traveled Distance
(km)		EEZ
(Days)
17896810-02-202108-01-202298.1311,395.4723.08
17897010-03-202108-30-2022331.914341.434.04
17897208-03-202109-27-202154.551045.7754.55
19684910-07-202110-20-202113.594262.1413.59
19685010-04-202111-08-202134.993471.4233.88
19685210-04-202111-15-202142.153228.0212.04
19685310-02-202110-29-202127.493324.2913.02
19685410-05-202111-03-202128.823138.7528.82
19685510-02-202110-27-202124.522004.1224.52
19685611-06-202101-01-202256.004026.6526.32
17897109-26-202210-01-20225.152369.535.15
19686010-06-202211-18-202243.003139.7043.00
22811210-01-202211-04-202234.453076.1828.83
22811410-14-202210-29-202214.491424.571.94
22811509-27-202311-03-202337.512508.0837.51
22811909-23-202310-17-202323.772675.8417.4
Table 2. Parameter estimates for behavioral states in the blue whale hidden Markov model.
Table 2. Parameter estimates for behavioral states in the blue whale hidden Markov model.
Model ParameterBehavioral StateValue
Step Length (km)Migratory60 ± 10
Foraging20 ± 10
Turning AngleMigratory0
Foragingπ
Table 3. Percentage of whales’ distribution area with respect to depth (m) and states (foraging and migrating) as estimated by the HMM model.
Table 3. Percentage of whales’ distribution area with respect to depth (m) and states (foraging and migrating) as estimated by the HMM model.
Depth (m)Foraging (%)Migrating (%)
0–2006.448.14
201–5002.218.35
501–10005.636.59
1001–15003.426.37
>150082.3070.55
Table 4. Model coefficient of correlation between each environmental variable (HMM model covariate) to the probabilities of switching between behavioral states (foraging and migration), with confidence intervals.
Table 4. Model coefficient of correlation between each environmental variable (HMM model covariate) to the probabilities of switching between behavioral states (foraging and migration), with confidence intervals.
From Foraging to Migrating StateFrom Migrating to Foraging State
Intercept−1.957 (−2.354, −1.560)−2.569 (−2.963, −2.174)
Chl−0.069 (−0.415, 0.276)0.057 (−0.347, 0.460)
Prod0.062 (−0.166, 0.290)0.070 (−0.228, 0.368)
SST−0.174 (−0.545, 0.197)−0.405 (−0.895, 0.085)
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Guzman, H.M.; Estévez, R.M.; Kaiser, S. Insights into Blue Whale (Balaenoptera musculus L.) Population Movements in the Galapagos Archipelago and Southeast Pacific. Animals 2024, 14, 2707. https://doi.org/10.3390/ani14182707

AMA Style

Guzman HM, Estévez RM, Kaiser S. Insights into Blue Whale (Balaenoptera musculus L.) Population Movements in the Galapagos Archipelago and Southeast Pacific. Animals. 2024; 14(18):2707. https://doi.org/10.3390/ani14182707

Chicago/Turabian Style

Guzman, Hector M., Rocío M. Estévez, and Stefanie Kaiser. 2024. "Insights into Blue Whale (Balaenoptera musculus L.) Population Movements in the Galapagos Archipelago and Southeast Pacific" Animals 14, no. 18: 2707. https://doi.org/10.3390/ani14182707

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