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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.
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
32 examination of the power to detect trends in whale abundance or predict ecosystem responses to climat
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
38 means of sound generation and transmission, whales and bats adaptively change their FOV, suggesting
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
44 emical variation in the cerebellum of beluga whales and Se may partially protect from MeHg-associated
46 al-based demographic data in resident killer whales and show that when mothers and daughters co-breed
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
56 in the liver and brain of long-finned pilot whales are attached to Se-rich structures and possibly a
58 trends is problematic, in part because minke whales are frequently sighted within Antarctic sea ice w
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
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
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
84 n and flowed passively into the mouth of the whale by the current created by the lower mandible break
86 but a few species such as humans and killer whales can live decades after their last reproduction.
89 a small species (~2.5 cm long), found near a whale carcass at 631 m depth in Monterey Submarine Canyo
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
95 ss the regions in our model, overall, killer whales consume the largest biomass of Chinook salmon, bu
97 ds, and large-scale redistributions of sperm whale cultural clans in the Pacific have likely changed
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
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
112 d hosts compared to other toothed and baleen whales, driven by differences in symbiont membership.
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
125 Most notably, we report evidence of bowhead whale exploitation by the Saqqaq culture 4,000 years ago
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
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
139 sequencing and de novo assembly of the minke whale genome, as well as the whole-genome sequences of t
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
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
150 sandersi, 2 hippos, and 23 fossil and extant whales in a phylogenetic context, we conclude that ultra
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.
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.
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
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
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
181 Introduction of a nonaxial His into sperm whale Mb at the topologically equivalent position and in
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
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
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
195 housand in delta(202)Hg values between pilot whale muscle tissue and Faroese whalers' hair but no mas
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
201 terns of the endangered North Atlantic right whale (NARW; Eubalaena glacialis) population in recent y
204 nge of animals, from fruit flies to humpback whales, operating in either air or water, natural propul
206 ineages uniquely associated with the toothed whales or Odontoceti (arginine at 156) and baleen whales
208 ion by three species of pinnipeds and killer whales (Orcinus orca) on Chinook salmon (Oncorhynchus ts
210 s in the endangered Southern Resident killer whale population by addressing modulation by prey availa
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
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
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.
226 discovery of tread-water feeding in Bryde's whales represents the first report of passive feeding in
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
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
243 l species of baleen whale, including rorqual whales, show active chasing and feeding, i.e., skimming,
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
250 ponses of long-finned pilot whales to killer whale sound playbacks and two anthropogenic sources of d
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
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.
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
269 These findings demonstrate that humpback whales trophically respond to ecosystem shifts, and as a
272 at are involved in sexual selection, toothed whales use learned signals in individual recognition and
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
279 receptor variant found in the larger baleen whales was functionally less responsive to its endogenou
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
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
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
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
300 he harbor porpoise were present in the minke whale, with no specific nuclei being absent, and no nove
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