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1 eric slow-wave sleep of odontocetes (toothed whales).
2 ately 44 minutes of recordings from a single whale.
3 dontocete cetaceans are present in the minke whale.
4 ed Australian and New Zealand southern right whale.
5 erea marginata, is the most enigmatic living whale.
6 ct from the typical lunge feeding of rorqual whales.
7 ifestyle different from that of other extant whales.
8 rns in FOSA concentrations measured in pilot whales.
9 multichannel rod-based signaling in balaenid whales.
10  shifts in the densities of migratory baleen whales.
11 ales reaching maximum gape earlier than blue whales.
12 ue long-term dataset on wild resident killer whales.
13 ra musculus) and fin (Balaenoptera physalus) whales.
14  known about the risk of exposure for beluga whales.
15 ys and stem teleost fishes, and in mysticete whales.
16 were associated with MeHg exposure in beluga whales.
17 ers exposed to MeHg predominantly from pilot whales.
18 cializations and feeding strategies in early whales.
19 ly within a clade removed from modern baleen whales.
20 ced by a variety of animals including baleen whales.
21 sitions between states in short-finned pilot whales.
22  for this low diversity, especially in sperm whales.
23 y recovering pinnipeds and endangered killer whales.
24 luding commercially important fish and great whales.
25 p to 61.5% for bigeyes and 87.4% for Bryde's whales.
26  and reproductive success in resident killer whales [9, 10].
27 enome sequences of three minke whales, a fin whale, a bottlenose dolphin and a finless porpoise.
28 iencephalon, midbrain, and pons of the minke whale, a mysticete cetacean.
29 as the whole-genome sequences of three minke whales, a fin whale, a bottlenose dolphin and a finless
30 ope profiles of 66 Australian southern right whales, a proxy for feeding ground location, and both mt
31  provide strong evidence of declining beaked whale abundance in the study area.
32 examination of the power to detect trends in whale abundance or predict ecosystem responses to climat
33 acific calving grounds remain at <10% of pre-whaling abundance.
34                       During engulfment, the whale accelerates, opens its jaw until it is almost perp
35  whale scat samples collected from 54 unique whales across a 4 year sampling period (2010-2013) were
36 he dorsal raphe nuclear complex of the minke whale, all indicate that the suite of neural characteris
37 d be detrimental to the North Atlantic Right Whale and a host of important fishery species.
38  means of sound generation and transmission, whales and bats adaptively change their FOV, suggesting
39                                              Whales and dolphins (Cetacea) have excellent social lear
40 nchronous changes in song patterns of baleen whales and experimental work on toothed whales in captiv
41  can help explain why female resident killer whales and humans continue to live long after they have
42  were observed on 58 occasions, involving 31 whales and including eight adult-calf pairs.
43 s transitional between raptorial archaeocete whales and modern mysticetes.
44 emical variation in the cerebellum of beluga whales and Se may partially protect from MeHg-associated
45 torical abundances of large animals, such as whales and sea turtles, is well known.
46 al-based demographic data in resident killer whales and show that when mothers and daughters co-breed
47               The strong association between whales and the dynamic, changing sea ice requires reexam
48  canyons that are suitable for Gray's beaked whales and their prey.
49 nternational Convention on the Regulation of Whaling and the failure to successfully regulate whaling
50 hanisms underlying song learning in humpback whales, and comparative perspectives on the evolution of
51 of canyons and seamounts to beaked and sperm whales, and quantified seasonal shifts in the densities
52 nternational Convention on the Regulation of Whaling, and the International Whaling Commission in par
53 sity of the completely helical protein sperm whale apomyoglobin (sw ApoMb) for amyloid formation from
54                                          Fin whales appear to synchronize and gradually modify song r
55 rgence of Odontocetes and Mystocetes (baleen whales) approximately 33-37 Mya.
56  in the liver and brain of long-finned pilot whales are attached to Se-rich structures and possibly a
57                                       Beaked whales are deep diving elusive animals, difficult to cen
58 trends is problematic, in part because minke whales are frequently sighted within Antarctic sea ice w
59 erves in the floor of the oral cavity of fin whales are highly extensible.
60                                       Beaked whales are hypothesized to be particularly sensitive to
61                        The songs of humpback whales are one of the most striking examples of the tran
62            The social relationships of sperm whales are organized in a multilevel society with an upp
63 nformation for monitoring of health in right whales, as well as a framework for integrating observati
64 ismatic marine megafauna from albatrosses to whales, as well as consuming carbon dioxide and producin
65  in ice conditions, affect the proportion of whales available to be counted by traditional shipboard
66 fundamental and overtone frequencies of blue whale B calls can be well modeled using a series of shor
67 . borealis), Bryde's whale (B. edeni), minke whale (B. acutorostrata), and humpback whale (Megaptera
68 tera musculus), fin whale (B. physalus), sei whale (B. borealis), Bryde's whale (B. edeni), minke wha
69  physalus), sei whale (B. borealis), Bryde's whale (B. edeni), minke whale (B. acutorostrata), and hu
70  the blue whale (Balaenoptera musculus), fin whale (B. physalus), sei whale (B. borealis), Bryde's wh
71 ed the retina of the closely related bowhead whale (Balaena mysticetus; family Balaenidae) to determi
72 se on the communication space of the Bryde's whale Balaenoptera edeni, an endangered species which vo
73 whales (Balaenopteridae), including the blue whale (Balaenoptera musculus), fin whale (B. physalus),
74 en reconstructed for an individual male blue whale (Balaenoptera musculus, Linnaeus 1758) using the e
75 y fitting tri-axial movement sensors to blue whales (Balaenoptera musculus), and by recording the dir
76                                      Rorqual whales (Balaenopteridae) are among the largest vertebrat
77 any previous studies have shown that rorqual whales (Balaenopteridae), including the blue whale (Bala
78 ble to filter-feeding duck beak lamellae and whale baleen plates, as well as the fluid mechanics of v
79                                    The minke whale-based feed contained a summation operatorPOPs conc
80 redominantly occurred at depth (>70 m), with whales being more likely to rotate clockwise around thei
81  the underwater behavior of a Baird's beaked whale (Berardius bairdii) from the first deployment of a
82  were given a diet of POP-contaminated minke whale blubber, whereas their eight male siblings were fe
83  our analysis of these features in the minke whale brain.
84 n and flowed passively into the mouth of the whale by the current created by the lower mandible break
85           Nerves in the mouth of the rorqual whale can double in length during feeding, without incur
86  but a few species such as humans and killer whales can live decades after their last reproduction.
87                    Our study also shows that whales can modulate their responses to fluctuating level
88                              The pygmy right whale, Caperea marginata, is the most enigmatic living w
89 a small species (~2.5 cm long), found near a whale carcass at 631 m depth in Monterey Submarine Canyo
90                                              Whales caught their prey using a series of coordinated m
91 ere significantly higher than those found in whales collected around the world prior to the spill.
92 Regulation of Whaling, and the International Whaling Commission in particular, for other internationa
93 minke whales is central to the International Whaling Commission's conservation and management work an
94                            Mediterranean fin whales comprise a genetically distinct population, liste
95 ss the regions in our model, overall, killer whales consume the largest biomass of Chinook salmon, bu
96 aling regulation after World War II, illegal whaling continued for decades [3].
97 ds, and large-scale redistributions of sperm whale cultural clans in the Pacific have likely changed
98          An annual increase in the number of whale deaths comparable to that observed during the summ
99 zone wedges (GZWs) on the outer shelf of the Whales Deep Basin.
100             High trophic level arctic beluga whales (Delphinapterus leucas) are exposed to persistent
101 ions have increased in western Arctic beluga whales (Delphinapterus leucas) since the industrial revo
102  been investigated for Pacific Arctic beluga whales (Delphinapterus leucas) that follow matrilineally
103 ntify the role of prey availability on right whale demographic transitional probabilities and use a c
104 gradient of ice conditions to estimate minke whale density in the Weddell Sea.
105                        In contrast, humpback whale diets are dominated by schooling fish when the NPG
106                                     Humpback whale diets captured two major shifts in oceanographic a
107 tion of predator vocalizations by male sperm whales disrupted functional behaviours and mediated prev
108 red with other feeding behaviors because the whales do not swim forward in pursuit of prey during the
109                         Odontocetes (toothed whales, dolphins and porpoises) hunt and navigate throug
110                    The exception is Cetacea (whales, dolphins, and porpoises), in which DG size, conv
111 aled diverse microbial communities in kogiid whales dominated by Firmicutes and Bacteroidetes.
112 d hosts compared to other toothed and baleen whales, driven by differences in symbiont membership.
113 ondition of these ice edge-associated beluga whales during these two years.
114                                 The use of a whale earplug to reconstruct lifetime chemical profiles
115 In this report, we describe a new xenorophid whale (Echovenator sandersi, gen. et sp.nov.) from the O
116 sent-day populations of North Pacific killer whale ecotypes have a complex ancestry, confounding the
117 genomic variation among North Pacific killer whale ecotypes resulting from multiple colonisation even
118 nalysing population genomic data from killer whale ecotypes, which we estimate have globally radiated
119 mediately before prey capture, both bats and whales emit a buzz with such high emission rates (>/= 18
120                                     In these whales, engulfment coincided largely with body decelerat
121                   Sequence analysis of right whale (Eubalaena glacialis; family Balaenidae) cDNA deri
122                                      Rorqual whales exhibit an extreme lunge filter-feeding strategy
123              Krill-feeding blue and humpback whales exhibited temporally distinct acceleration and en
124           The ventral grooved blubber in fin whales expands by an estimated 162% in the circumferenti
125  Most notably, we report evidence of bowhead whale exploitation by the Saqqaq culture 4,000 years ago
126                       After the discovery of whale fall communities in modern oceans, it has been hyp
127 ones prior to final burial, unlike in modern whale falls where organisms such as the ubiquitous bone-
128 ulfilled similar ecological roles to shallow whale falls, and did not support specialized chemosynthe
129  Mass stranding of several species of beaked whales (family Ziphiidae) associated with exposure to an
130  that have ever lived on Earth (Blue and Fin whales) feed in the Arctic and Southern Oceans.
131 oth the downward and upward direction of the whale (Figure S1).
132 al function for the uniquely shaped humpback whale flipper.
133 t by synchronously tracking predator (killer whales, [Formula: see text] = 1; representing a family g
134 he paleotopographic implications of a beaked whale fossil (Ziphiidae) from the Turkana region of Keny
135 re not significant, supporting the idea that whales from different calving grounds mix in migratory c
136 nearities in the song repertoire of humpback whales from the Ste Marie channel (Madagascar) to provid
137 sue was sampled from hunter-harvested beluga whales from the western Canadian Arctic in 2008 and 2010
138                   Here, we sequenced the fin whale genome and analysed FGFs from 8 cetaceans.
139 sequencing and de novo assembly of the minke whale genome, as well as the whole-genome sequences of t
140                                  Overall the whale-genome sequences exhibited distinct features that
141 whales (Orcinus orca) and short-finned pilot whales (Globicephala macrorhynchus) [3, 4]-have comparab
142 scle from juvenile male North Atlantic pilot whales (Globicephala melas) harvested between 1986 and 2
143 g activity to free-ranging long-finned pilot whales (Globicephala melas).
144 ey availability and/or an expansion of right whale habitat into unprotected waters.
145  GOM site, both Gervais' and Cuvier's beaked whales had a high density throughout the monitoring peri
146 ured the duration of feeding events when the whales had a wide-open mouth mostly above the sea surfac
147 -reproductive females can explain why killer whales have evolved the longest post-reproductive lifesp
148 ses in Arctic killer whale sightings, killer whales have the potential to reshape Arctic marine mamma
149 ansduces the lowest frequencies of the pilot whales hearing spectrum.
150 sandersi, 2 hippos, and 23 fossil and extant whales in a phylogenetic context, we conclude that ultra
151 leen whales and experimental work on toothed whales in captivity.
152 markers in different brain regions of beluga whales in order to assess potential neurotoxicological r
153 rom two mass strandings of long-finned pilot whales in Scotland were processed for scanning electron
154 nd shows that the resulting SPPR for toothed whales in the Icelandic marine ecosystem is 2.8 times hi
155 he past was a world of giants, with abundant whales in the sea and large animals roaming the land.
156  ppm in tissue collected from Gulf of Mexico whales in the wake of the crisis.
157 RPA I, JARPA II) and the origins of the case Whaling in the Antarctic (Australia v.
158             Generally, all species of baleen whale, including rorqual whales, show active chasing and
159 nfunctional in Odontoceti cetaceans (toothed whales, including dolphins and orcas).
160 thin 3 minutes of exposure onset, the tagged whale increased swim speed and body movement, and contin
161 nook salmon consumed by pinnipeds and killer whales increased from 6,100 to 15,200 metric tons (from
162  become silent (21% of cases), whereas pilot whales increased surface resting during sonar exposure.
163  The surveys revealed substantial numbers of whales inside the sea ice.
164          Culture seems to have driven killer whales into distinct ecotypes, which may be incipient sp
165 ssion seems key in the partitioning of sperm whales into sympatric clans.
166      Estimating abundance of Antarctic minke whales is central to the International Whaling Commissio
167 t subsurface behaviour in short-finned pilot whales is more complex than a simple dichotomy of deep a
168       Diving behaviour of short-finned pilot whales is often described by two states; deep foraging a
169 ts role in attenuating Hg toxicity in beluga whales is poorly understood.
170  during a lunge can exceed the volume of the whale itself [2].
171                                       When a whale kept its upper jaw above the sea surface, many anc
172 old and represents the oldest derived beaked whale known, consistent with molecular estimates of the
173 polar bears (PB; Ursus maritimus) and killer whales (KW; Orcinus orca) were used for in vitro concent
174 (SDs), bottlenose dolphins (BNDs) and killer whales (KWs) had mean PCB levels that markedly exceeded
175 , mirroring the empirical clans, emerge when whales learn preferentially the most common codas (confo
176                                 While baleen whales like many vocal learners use this skill in song d
177 ly, Caperea represents the only major baleen whale lineage entirely restricted to the Southern Ocean.
178 omic analysis identified an expansion in the whale lineage of gene families associated with stress-re
179 pecies of larger mammal bones such as bison, whale, llama, etc., the calibration curve showed a slowe
180                             The evolution of whales marks one of the major transitions in the history
181    Introduction of a nonaxial His into sperm whale Mb at the topologically equivalent position and in
182         HNE became covalently bound to sperm whale Mb at up to five sites based on ESI-MS analysis.
183 mussel tissue, squid muscle, crab claw meat, whale meat, cod muscle, Greenland halibut muscle and dog
184 minke whale (B. acutorostrata), and humpback whale (Megaptera novaeangliae), employ a strategy called
185        Compared to other cetaceans, humpback whales (Megaptera novaeangliae) have disproportionately
186 il feeding, through a population of humpback whales (Megaptera novaeangliae) over a period of 27 year
187 el of the human tooth and the rostrum of the whale Mesoplodon densirostris are two highly mineralized
188 yptic deep ocean cetacean, the Gray's beaked whale (Mesoplodon grayi).
189 tes of the emergence of modern strap-toothed whales (Mesoplodon).
190 tial amino acid synthesis pathways in baleen whale microbiomes more closely resemble those of terrest
191 he first phenological study examining beluga whale migrations within the context of their rapidly tra
192 cies (Chinese hamster, elephant shark, minke whale), 'mined the web' for DNA sequences and expanded t
193 o understanding and tracking shifts in large whale movements over long time scales.
194                                       In fin whales, multiple lunges can occur during a single dive,
195 housand in delta(202)Hg values between pilot whale muscle tissue and Faroese whalers' hair but no mas
196                 Engineered variants of sperm whale myoglobin catalyze this synthetically valuable C-C
197  site within the heme distal pocket of sperm whale myoglobin has offered well-defined diiron clusters
198  3-dimensional structure of a protein, sperm-whale myoglobin, worthy of a Nobel Prize in Chemistry in
199 iverged from the ancestors of filter-feeding whales (mysticetes).
200            Rorquals differ from other baleen whales (Mysticeti) in possessing longitudinal furrows or
201 terns of the endangered North Atlantic right whale (NARW; Eubalaena glacialis) population in recent y
202                     Three ecotypes of killer whale occur in partial sympatry in the North Pacific.
203 rding tags (DTAGs) deployed on 20 individual whales off Cape Hatteras, North Carolina, USA.
204 nge of animals, from fruit flies to humpback whales, operating in either air or water, natural propul
205 s or Odontoceti (arginine at 156) and baleen whales or Mysticeti (glutamine at 156).
206 ineages uniquely associated with the toothed whales or Odontoceti (arginine at 156) and baleen whales
207                Only two other species-killer whales (Orcinus orca) and short-finned pilot whales (Glo
208 ion by three species of pinnipeds and killer whales (Orcinus orca) on Chinook salmon (Oncorhynchus ts
209 fferentiated sympatric populations of killer whales (Orcinus orca).
210 s in the endangered Southern Resident killer whale population by addressing modulation by prey availa
211                     The North Atlantic right whale population is currently the focus of conservation
212  Contrary to previous predictions, the right whale population is projected to recover in the future a
213 tically endangered, Southern Resident killer whale population of the northeastern Pacific Ocean provi
214 ry and ecological importance of songs to fin whale populations is needed.
215 nd widespread population reductions in great whale populations over the past few centuries.
216 che modelling, and showed that 80% of tagged whale positions was near (<7 km) the closest suitable ha
217 ts indicate a northward range shift in right whale prey, potentially resulting in decreased prey avai
218 ly with body deceleration; however, humpback whales pursuing more agile fish demonstrated highly vari
219           This strategy involves the rorqual whale rapidly engulfing a huge volume of prey-laden wate
220 Testosterone profiles suggest this male blue whale reached sexual maturity at approximately 10 y of a
221 eration and engulfment phases, with humpback whales reaching maximum gape earlier than blue whales.
222 ita, at 1.4 meters and the largest, the blue whale, reaching 33 meters.
223                                      Despite whaling regulation after World War II, illegal whaling c
224                         Odontocetes (toothed whales) rely upon echoes of their own vocalizations to n
225  steadily for 10 d, the duration that killer whales remained in Admiralty Inlet.
226  discovery of tread-water feeding in Bryde's whales represents the first report of passive feeding in
227                 I then describe the Japanese Whale Research Programs Under Special Permit in the Anta
228                          We examine humpback whale response to environmental variability through stab
229  strategy that conveys information about the whale's body size and physical fitness, and thus may be
230 efficiency of foraging is driven both by the whale's engulfment capacity and the comparative locomoto
231 ow-dimensional biomechanical modeling of the whale's U-fold (vocal folds homolog) is used to relate s
232                        A total of 140 killer whale scat samples collected from 54 unique whales acros
233                                          The whale shark (Rhincodon typus) is the largest extant spec
234 es of Fauna and Flora (CITES), including the whale shark (Rhincodon typus), which was surprisingly fo
235 tion, number and arrangement of the genes in whale shark mitogenome are the same as found in the mito
236 niformes and Carcharhiniformes, although the whale shark mitogenome had a slightly longer control reg
237 e also performed comparative analysis of the whale shark mitogenome to the available mitogenome seque
238 the mitochondrial genome (mitogenome) of the whale shark obtained by next-generation sequencing metho
239   The availability of mitogenome sequence of whale shark will aid studies of molecular systematics, b
240 spension-feeding fishes such as goldfish and whale sharks retain prey without clogging their oral fil
241 M sleep, it is unclear whether the mysticete whales show a similar sleep pattern.
242                                       Killer whales show strong specialization on prey choice in popu
243 l species of baleen whale, including rorqual whales, show active chasing and feeding, i.e., skimming,
244                                              Whales showing this behavior were observed on 58 occasio
245 t has been suggested that the lack of beaked whale sightings is the result of their low abundance, bu
246 ns in sea ice and increases in Arctic killer whale sightings, killer whales have the potential to res
247                                          Fin whale songs were analyzed from data collected from 2000-
248                                          Fin whale songs, which consist of short pulses repeated at r
249 us may be an important component of humpback whale songs.
250 ponses of long-finned pilot whales to killer whale sound playbacks and two anthropogenic sources of d
251                                         Blue whale sound production has been thought to occur by Helm
252                                       Killer whale sounds elicited increased calling rates and the ag
253                                       Beaked whale species detected include: Gervais' (Mesoplodon eur
254                          The four key baleen whale species of the region: fin, humpback, blue and min
255 nsion with evidence that caribou, walrus and whale species played a more prominent role for the survi
256 rrent information, it seems that some beaked whale species require relatively high quality habitat in
257 tic foraging behavior in this largest beaked whale species, and the first experimental demonstration
258                 Our analysis also identified whale-specific mutations in genes encoding antioxidants
259 Sea, the endangered Southern Resident Killer Whale (SRKW) is a high trophic indicator of ecosystem he
260  models, we show that the presence of killer whales strongly alters the behavior and distribution of
261 ing and the failure to successfully regulate whaling that led to the commercial moratorium in 1986.
262                                    In killer whales the ecotype divisions, together with founding bot
263 f emerged by convergent evolution in toothed whales, the only other mammals with a prolonged post-rep
264 ordination, suggesting that, in social pilot whales, this could drive behavioural responses to distur
265 d for measuring POP concentrations in killer whales through scat employed in this study may improve t
266  investigated responses of long-finned pilot whales to killer whale sound playbacks and two anthropog
267 is an active sense enabling bats and toothed whales to orient in darkness through echo returns from t
268                                          The whale traveled from the Indian Ocean inland along an eas
269     These findings demonstrate that humpback whales trophically respond to ecosystem shifts, and as a
270                 Southern hemisphere humpback whales undertake the longest migrations and associated p
271                                          All whales undertook mid- to long-distance migrations, cross
272 at are involved in sexual selection, toothed whales use learned signals in individual recognition and
273                                      Toothed whales use sonar to detect, locate, and track prey.
274 esented for the density estimation of beaked whales, using passive acoustic monitoring data collected
275      This implies that the frequency of blue whale vocalizations might be directly proportional to th
276 hypothesis, we conducted playbacks of killer whale vocalizations recorded during herring-feeding acti
277  three species of marine mammals (the killer whale, walrus and manatee) from three mammalian orders t
278 he shift from terrestrial to aquatic life by whales was a substantial evolutionary event.
279  receptor variant found in the larger baleen whales was functionally less responsive to its endogenou
280 rom Beaufort Sea foraging regions by Chukchi whales was postponed in the late period.
281             For Gervais' and Cuvier's beaked whales, we estimated weekly animal density using two met
282 ci) and sex from 128 individually-identified whales, we find significant differentiation among winter
283 he oil, and their elevated concentrations in whales, we suggest that metal exposure is an important u
284  Yakut horse, Mammoth, Polar bear, and Minke whale were chosen.
285           Between 2012 and 2015 thirteen fin whales were equipped with satellite transmitters, 8 in t
286 ralization were related to where and how the whales were feeding in the water column.
287                                  When killer whales were present (within about 100 km), narwhal moved
288 t the monitoring period, but Cuvier's beaked whales were present only seasonally, with periods of low
289 wo sites in the western GOM, Gervais' beaked whales were present throughout the monitoring period, bu
290                Recordings of living humpback whales were searched for occurrences of vocal nonlineari
291  (Kogia breviceps) and dwarf (K. sima) sperm whales were used to characterize the gut microbiomes of
292 ue long-term dataset on wild resident killer whales, where females can live decades after their final
293 el is similar to those proposed for humpback whales, where valve open/closure and vocal fold oscillat
294 ed from those previously reported in toothed whales, which exhibited low diversity communities domina
295       In the upper Gulf of Thailand, Bryde's whales, which feed on small fish species [3], predominan
296 he first report of passive feeding in baleen whales, which indicates their flexible capacity to modif
297 escribes the head-lifting feeding by Bryde's whales, which is distinct from the typical lunge feeding
298                     Here we show that baleen whales, which prey on animals (fish and crustaceans), ha
299                          The five species of whale with matrilineal social systems have remarkably lo
300 he harbor porpoise were present in the minke whale, with no specific nuclei being absent, and no nove

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