Baleen whales influence their ecosystems through immense prey consumption and nutrient recycling
. It is difficult to accurately gauge the magnitude of their current or historic ecosystem role ...without measuring feeding rates and prey consumed. To date, prey consumption of the largest species has been estimated using metabolic models
based on extrapolations that lack empirical validation. Here, we used tags deployed on seven baleen whale (Mysticeti) species (n = 321 tag deployments) in conjunction with acoustic measurements of prey density to calculate prey consumption at daily to annual scales from the Atlantic, Pacific, and Southern Oceans. Our results suggest that previous studies
have underestimated baleen whale prey consumption by threefold or more in some ecosystems. In the Southern Ocean alone, we calculate that pre-whaling populations of mysticetes annually consumed 430 million tonnes of Antarctic krill (Euphausia superba), twice the current estimated total biomass of E. superba
, and more than twice the global catch of marine fisheries today
. Larger whale populations may have supported higher productivity in large marine regions through enhanced nutrient recycling: our findings suggest mysticetes recycled 1.2 × 10
tonnes iron yr
in the Southern Ocean before whaling compared to 1.2 × 10
tonnes iron yr
recycled by whales today. The recovery of baleen whales and their nutrient recycling services
could augment productivity and restore ecosystem function lost during 20th century whaling
.
One of the lesser known species of baleen whales, the Bryde’s whale, also known as Eden’s whale (Balaenoptera edeni edeni and B. edeni brydei), although hunted as part of a North Pacific Japanese ...research programme , was not heavily exploited by commercial whaling and remains a data deficient species. Their taxonomic status is not fully resolved and they are often mistaken for other species leading to uncertainty about their true distribution, behavior and conservation status. Some populations are critically endangered, whilst others are small but have high genetic diversity suggesting wider connectivity. The species’ unpredictable coastal and offshore global distribution throughout warm-temperate waters has led to populations with unknown genetic variation, and facing different threats. Few areas are well-studied, but each study reveals often contrasting movement patterns, foraging strategies and vocal repertoires; there are considerable knowledge gaps for Bryde’s whales. There are few Bryde’s populations with abundance estimates but they typically number in the mid- to high-hundreds of individuals, with other populations small, <100 mature individuals, and exposed to high levels of anthropogenic impacts. Future research should focus on understanding the diversity within and between populations. Here, we suggest an integrative, comparative approach towards future work on Bryde’s whales, including acoustic monitoring, trophic interactions, telemetry tools, understanding their novel behaviors, and resolving their species status. This will inform conservation management of this unusual species of whale vulnerable to anthropogenic impacts.
The considerable power needed for large whales to leap out of the water may represent the single most expensive burst maneuver found in nature. However, the mechanics and energetic costs associated ...with the breaching behaviors of large whales remain poorly understood. In this study we deployed whale-borne tags to measure the kinematics of breaching to test the hypothesis that these spectacular aerial displays are metabolically expensive. We found that breaching whales use variable underwater trajectories, and that high-emergence breaches are faster and require more energy than predatory lunges. The most expensive breaches approach the upper limits of vertebrate muscle performance, and the energetic cost of breaching is high enough that repeated breaching events may serve as honest signaling of body condition. Furthermore, the confluence of muscle contractile properties, hydrodynamics, and the high speeds required likely impose an upper limit to the body size and effectiveness of breaching whales.
Despite their enormous size, whales make their living as voracious predators. To catch their much smaller, more maneuverable prey, they have developed several unique locomotor strategies that require ...high energetic input, high mechanical power output and a surprising degree of agility. To better understand how body size affects maneuverability at the largest scale, we used bio-logging data, aerial photogrammetry and a high-throughput approach to quantify the maneuvering performance of seven species of free-swimming baleen whale. We found that as body size increases, absolute maneuvering performance decreases: larger whales use lower accelerations and perform slower pitch-changes, rolls and turns than smaller species. We also found that baleen whales exhibit positive allometry of maneuvering performance: relative to their body size, larger whales use higher accelerations, and perform faster pitch-changes, rolls and certain types of turns than smaller species. However, not all maneuvers were impacted by body size in the same way, and we found that larger whales behaviorally adjust for their decreased agility by using turns that they can perform more effectively. The positive allometry of maneuvering performance suggests that large whales have compensated for their increased body size by evolving more effective control surfaces and by preferentially selecting maneuvers that play to their strengths.
Bryde’s whales (
Balaenoptera edeni
) are medium-sized balaenopterids with tropical and subtropical distribution. There is confusion about the number of species, subspecies and populations of Bryde’s ...whale found globally. Two eco-types occur off South Africa, the inshore and offshore forms, but with unknown relationship between them. Using the mtDNA control region we investigated the phylogenetic relationship of these populations to each other and other Bryde’s whale populations. Skin, baleen and bone samples were collected from biopsy-sampled individuals, strandings and museum collections. 97 sequences of 674 bp (bp) length were compared with published sequences of Bryde’s whales (n = 6) and two similar species, Omura’s (
B. omurai
) and sei (
B. borealis
) whales (n = 3). We found eight haplotypes from the study samples: H1–H4 formed a distinct, sister clade to pelagic populations of Bryde’s whales (
B. brydei
) from the South Pacific, North Pacific and Eastern Indian Ocean. H5–H8 were included in the pelagic clade. H1–H4 represented samples from within the distributional range of the inshore form. Pairwise comparisons of the percentage of nucleotide differences between sequences revealed that inshore haplotypes differed from published sequences of
B. edeni
by 4.7–5.5% and from
B. brydei
by 1.8–2.1%. Ten fixed differences between inshore and offshore sequences supported 100% diagnosability as subspecies. Phylogenetic analyses grouped the South African populations within the Bryde’s-sei whale clade and excluded
B. edeni
. Our data, combined with morphological and ecological evidence from previous studies, support subspecific classification of both South African forms under
B. brydei
and complete separation from
B. edeni
.
Recent changes in the South African marine ecosystem and the introduction of an experimental octopus fishery have resulted in an unsustainably high rate of fatal Bryde's whale entanglements. Using ...suction‐cup attached bio‐loggers, we identified a previously undescribed feeding behavior used by Bryde's whales to catch prey, and this behavior may make them susceptible to entanglement and mortality in bottom‐mounted fishing gear. As they chase down their prey, inshore Bryde's whales sprint and maneuver along the seafloor for extended periods of time, making multiple direction changes, and reaching extraordinarily high swimming speeds. These findings assisted in the implementation of mandatory changes to octopus fishing gear that have drastically reduced the number of entanglements. The novel finding that Bryde's whales use high‐speed chases near the seafloor to catch their prey highlights the value of using species‐specific, behavioral information for making conservation recommendations.
Alloparental care is defined as any behavior by an individual towards non-descendant young that benefits the young. This can occur through indirect behaviors such as herding and sentinel behavior or ...directly through behaviors such as babysitting, provisioning, and adoption. The best-documented case of interspecific alloparental care in cetaceans involves the complete adoption of a melon-headed whale (Peponocephala electro) calf by a female common bottlenose dolphin (Tursiops truncatus) at Rangiroa atoll, French Polynesia. The association between the primiparous female, which had a dependant biological calf when the adoption occurred, and the adoptee continued for 4 years during winch time nursing was evident.
Celotno besedilo
Dostopno za:
DOBA, IZUM, KILJ, NUK, PILJ, PNG, SAZU, UILJ, UKNU, UL, UM, UPUK
Vagrant southern elephant seals (
Mirounga leonina
) are occasionally sighted along the coast of South Africa and are known to feed primarily on fish and squid. Phocid seals are not known to predate ...on mammals making the events described here exceptional. This note describes the successful and failed attempts of a vagrant male southern elephant seal (
M. leonina)
to consume Cape fur seal (
Arctocephalus pusillus pusillus)
pups in Plettenberg Bay, South Africa. Observations were made by crew and passengers aboard a commercial whale-watching vessel during November 2012. This is the first account of elephant seals eating anything other than fish, squid and penguins and suggests considerable plasticity in prey choice dictated by environmental conditions.
The biology of South African Bryde’s whales (Balaenoptera brydei/edeni), with a focus on the inshore form, was investigated through estimates of abundance and survival rate, seasonality of occurrence ...and variation in mitochondrial and nuclear DNA. Photographs, sightings data and biopsy samples were collected in Plettenberg Bay, on the south-east coast of South Africa. Additional genetic material was obtained from the Iziko South African Museum, Marine and Coastal Management, and the Port Elizabeth Museum. Mark-recapture methods applied to photo-identification data were used to estimate abundance and survival rate. Estimates of abundance ranged from 130 to 250 (CV = 0.07 - 0.38) and the estimated annual survival rate was 0.93 (CV = 0.047, 95% CI = 0.852 - 1.0). Seasonal increases in the encounter rate and number of individual whales were observed during summer and autumn, with a peak in April, which corresponded to increased feeding activity and larger average aggregation sizes. Chlorophyll-a, sea surface temperature and wind speed were all significant factors in explaining the variability in the occurrence of whales. No seasonality in the occurrence of calves was detected. Mitochondrial DNA control region sequences (685bp) were compared to published sequences. This confirmed the offshore form as Balaenoptera brydei and the inshore form as closely related to B.brydei, possibly at the sub-specific level, but excluded it as B.edeni. Phylogenetic analyses support complete separation between the two forms. The use of 10 polymorphic microsatellite loci revealed no population structure among the inshore samples (FST = 0.006). Pairwise estimates of relatedness found most individuals to be unrelated, with only a few distant relatives detected.
The biology of South African Bryde’s whales (Balaenoptera brydei/edeni), with a focus on the inshore form, was investigated through estimates of abundance and survival rate, seasonality of occurrence ...and variation in mitochondrial and nuclear DNA. Photographs, sightings data and biopsy samples were collected in Plettenberg Bay, on the south-east coast of South Africa. Additional genetic material was obtained from the Iziko South African Museum, Marine and Coastal Management, and the Port Elizabeth Museum. Mark-recapture methods applied to photo-identification data were used to estimate abundance and survival rate. Estimates of abundance ranged from 130 to 250 (CV = 0.07 - 0.38) and the estimated annual survival rate was 0.93 (CV = 0.047, 95% CI = 0.852 - 1.0). Seasonal increases in the encounter rate and number of individual whales were observed during summer and autumn, with a peak in April, which corresponded to increased feeding activity and larger average aggregation sizes. Chlorophyll-a, sea surface temperature and wind speed were all significant factors in explaining the variability in the occurrence of whales. No seasonality in the occurrence of calves was detected. Mitochondrial DNA control region sequences (685bp) were compared to published sequences. This confirmed the offshore form as Balaenoptera brydei and the inshore form as closely related to B.brydei, possibly at the sub-specific level, but excluded it as B.edeni. Phylogenetic analyses support complete separation between the two forms. The use of 10 polymorphic microsatellite loci revealed no population structure among the inshore samples (FST = 0.006). Pairwise estimates of relatedness found most individuals to be unrelated, with only a few distant relatives detected.
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