Killer whales (Orcinus orca) attack and kill a Bryde's whale (Balaenoptera edeni)

1990 ◽  
Vol 68 (7) ◽  
pp. 1603-1606 ◽  
Author(s):  
Gregory K. Silber ◽  
Michael W. Newcomer ◽  
Héctor Pérez-Cortés M.

On 3 May 1988, we observed a group of killer whales that pursued, killed, and partially consumed a Bryde's whale in the northern Gulf of California, Mexico (31°01′N, 114°15′W). The attack was observed from 06:54 to 08:53 while circling in a single-engine aircraft at an altitude of 160 m. The group comprised about 15 killer whales, including two adult males and at least two calves. Females and (or) subadult males pressed the attack most intently. The killer whales tore skin and blubber from the right flank of the Bryde's whale, and on 11 occasions the killer whales swam onto the head or back of the Bryde's whale, which hindered its breathing. The respiration intervals of the Bryde's whale were short and irregular, and blow rates differed significantly from those of undisturbed Bryde's whales. Fatiguing the whale may have facilitated an easier kill by asphyxiation. After the death of the Bryde's whale, the two adult male killer whales surfaced slowly about 200–300 m away from the remainder of the group, which presumably fed on the submerged Bryde's whale carcass. Two days later, the drifting Bryde's whale carcass was located. A large wound was visible on the abdomen, and sections of the lower jaw had been removed. Like those of canids and some felids that hunt cooperatively when preying on ungulates, attacks by Orcinus orca exhibit coordination of activities and efficiency in dispatching prey.

ARCTIC ◽  
2009 ◽  
Vol 61 (1) ◽  
pp. 102 ◽  
Author(s):  
Martin Renner ◽  
Kevin Bell

We observed a white adult male killer whale (Orcinus orca) on 7 August 2000 off the north side of Adak Island, Aleutians. An open saddle and a rounded dorsal fin tip suggest that this whale belongs to the fish-eating (“resident”) ecotype. A circular scar matching a cookie-cutter shark (Isistius sp.) bite mark suggested that the animal originated in warmer waters. Photographs and description provided here should enable individual identification should this animal be seen again.


2006 ◽  
Vol 32 (3) ◽  
pp. 265-272 ◽  
Author(s):  
Mercedes Guerrero-Ruiz ◽  
Héctor Pérez-Cortés M. ◽  
Mario Salinas Z. ◽  
Jorge Urbán R.

Author(s):  
Sanna Kuningas ◽  
Tiu Similä ◽  
Philip S. Hammond

A long-term photo-identification study of killer whales (Orcinus orca) in northern Norway was initiated in 1986, when their prey the Norwegian spring-spawning herring (Clupea harengus) started to winter in a complex fjord system. The aim of this work was to estimate population size and apparent survival rates in this killer whale population using photo-identification and mark–recapture techniques with data collected during October–December 1986–2003. Total population size was estimated to be highest in 2003: 731 individuals (SE = 139, 95% CI = 505–1059) using a model taking heterogeneity of capture probabilities into account. Apparent survival of adult males and adult females was estimated using the Cormack–Jolly–Seber model as 0.971 (SE = 0.008) and 0.977 (SE = 0.009), respectively. Calving intervals ranged from 3 to 14 years (mean = 5.06, SE = 0.722). These are the first estimates of northern Norwegian killer whale population parameters, allowing their dynamics to be investigated and comparisons to be made with killer whale populations globally.


2013 ◽  
Vol 30 (3) ◽  
pp. 1229-1237 ◽  
Author(s):  
Graham A. J. Worthy ◽  
Tamara A. M. Worthy ◽  
Pamela K. Yochem ◽  
Christopher Dold

2010 ◽  
Vol 88 (11) ◽  
pp. 1103-1112 ◽  
Author(s):  
Patrick James O’Malley Miller ◽  
Ari Daniel Shapiro ◽  
Volker Bernt Deecke

Mammal-eating killer whales ( Orcinus orca (L., 1758)) are a rare example of social predators that hunt together in groups of sexually dimorphic adults and juveniles with diverse physiological diving capacities. Day–night ecological differences should also affect diving as their prey show diel variation in activity and mammal-eating killer whales do not rely on echolocation for prey detection. Our objective was to explore the extent to which physiological aerobic capacities versus ecological factors shape the diving behaviour of this breath-hold diver. We used suction-cup-attached depth recorders (Dtags) to record 7608 dives of 11 animals in southeast Alaska. Analysis of dive sequences revealed a strong bout structure in both dive depth and duration. Day–night comparisons revealed reduced rates of deep dives, longer shallow dives, and shallower long-duration dives at night. In contrast, dive variables did not differ by age–sex class. Estimates of the aerobic dive limit (cADL) suggest that juveniles exceeded their cADL during as much as 15% of long dives, whereas adult males and females never exceeded their cADL. Mammal-eating killer whales in this area appear to employ a strategy of physiological compromise, with smaller group members diving nearer their physiological limits and large-bodied males scaling down their physiological performance.


2019 ◽  
Vol 133 (2) ◽  
pp. 252-261 ◽  
Author(s):  
Yulán Úbeda ◽  
Sara Ortín ◽  
Judy St. Leger ◽  
Miquel Llorente ◽  
Javier Almunia

1973 ◽  
Vol 72 (2) ◽  
pp. 330-344 ◽  
Author(s):  
Peter Doerr

ABSTRACT A hapten-radioimmunoassay for plasma oestradiol is described and information about the reliability of the method is given in detail. Oestradiol-3-hemisuccinate coupled to keyhole limpet haemocyanin is used for immunization of rabbits. The antiserum utilized for the assay is characterized by its titer, affinity and specificity. Following ether extraction and NaOH-light petroleum partition oestradiol is separated from crossreacting oestrogens by TLC. Oxidation of oestradiol on the plate is prevented by mercaptoethanol. To separate free and antibody bound ligand 250 μg dextran-coated charcoal per tube is used in the presence of bovine serum gammaglobulin (1 mg/ml). The between-assay precision based on 15 different determinations of control samples from normal adult male plasma was 9.4% (C. V.). The mean reagent blank value of 31 determinations was equivalent to 0.3 pg oestradiol and the detection limit in terms of the 99% confidence limit for a single blank value, was equivalent to 4.3 pg oestradiol. A procedure for detecting plasma blanks is described. Plasma oestradiol is separated from approximately all concomitant substances originally present in the sample by enzymatic conversion into oestrone and a second TLC. No plasma blanks could be detected with respect to normal adult male plasma. Normal values for adult males based on 51 subjects were characterized by a median of 17.2 pg/ml and the 95 percentiles of 9.5–27.6.


2019 ◽  
Vol 8 (2) ◽  
Author(s):  
Takashi Matsushita ◽  
Tomoyasu Kumano ◽  
Kazuhiko Takehara

Primary cutaneous follicle center lymphoma (PCFCL) accounts for the majority of primary cutaneous B-cell lymphomas. We report a 60-year-old womanwith PCFCL. She had a red nodule (25 × 25 mm) on the right side of the lower jaw. She was diagnosed with PCFCL by skin biopsy. And then, she was treated with radiation therapy (total 30.6 Gy), which completely eliminated the nodule. Our case suggests that radiation therapy may be a first choice for PCFCL patients with a solitary lesion or localized lesions.    


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