|A fin whale surfaces in the Kenai Fjords, Alaska|
|Size compared to an average human|
|Fin whale range|
The fin whale (Balaenoptera physalus), also called the finback whale, razorback, or common rorqual, is a marine mammal belonging to the suborder of baleen whales. It is the second-largest animal after the blue whale. The largest reportedly grow to 27.3 m (89.6 ft) long with a maximum confirmed length of 25.9 m (85 ft), a maximum recorded weight of nearly 74 tonnes (73 long tons; 82 short tons), and a maximum estimated weight of around 120 tonnes (132.5 tons). American naturalist Roy Chapman Andrews called the fin whale "the greyhound of the sea... for its beautiful, slender body is built like a racing yacht and the animal can surpass the speed of the fastest ocean steamship."
The fin whale's body is long and slender, coloured brownish-grey with a paler underside.The fin whale is a large baleen whale that belongs to the cetacean order, which is composed of all species of whale, dolphin and porpoise. At least two recognized subspecies exist, in the North Atlantic and the Southern Hemisphere. It is found in all the major oceans, from polar to tropical waters. It is absent only from waters close to the ice pack at the poles and relatively small areas of water away from the open ocean. The highest population density occurs in temperate and cool waters. Its food consists of small schooling fish, squid, and crustaceans including copepods and krill.
Like all other large whales, the fin whale was heavily hunted during the 20th century and is an endangered species. Over 725,000 fin whales were reportedly taken from the Southern Hemisphere between 1905 and 1976, as of 1997 survived by only 38,000.
The International Whaling Commission (IWC) issued a moratorium on commercial hunting of this whale, although Iceland and Japan have resumed hunting. The species is also hunted by Greenlanders under the IWC's Aboriginal Subsistence Whaling provisions. Global population estimates range from less than 100,000 to roughly 119,000.
- 1 Taxonomy
- 2 Anatomy
- 3 Life history
- 4 Ecology
- 5 Human interaction
- 6 Conservation
- 7 See also
- 8 Footnotes
- 9 References
- 10 External links
The fin whale was first described by Friderich Martens in 1675 and then again by Paul Dudley in 1725. The former description was used as the primary basis of the species Balaena physalus by Carl Linnaeus in 1758. In 1804, Bernard Germain de Lacépède reclassified the species as Balaenoptera rorqual, based on a specimen that had stranded on Île Sainte-Marguerite (Cannes, France) in 1798. In 1830, Louis Companyo described a specimen that had stranded near Saint-Cyprien, southern France, in 1828 as Balaena musculus. Most later authors followed him in using the specific name musculus, until Frederick W. True (1898) showed that it referred to the blue whale. In 1846, British taxonomist John Edward Gray described a 16.7 m (55 ft) specimen from the Falkland Islands as Balaenoptera australis. In 1865, German naturalist Hermann Burmeister described a roughly 15 m (49 ft) specimen found near Buenos Aires about 30 years earlier as Balaenoptera patachonicus. In 1903, Romanian scientist Emil Racoviță placed all these designations into Balaenoptera physalus. The word physalus comes from the Greek word physa, meaning "blows", referring to the prominent blow of the species (as described by Martens [1675, p. 132]: "They know the finn-fish by the... vehement blowing and spouting up of the water...").
Fin whales are rorquals, members of the family Balaenopteridae, which also includes the humpback whale, the blue whale, Bryde's whale, the sei whale, and the minke whales. The family diverged from the other baleen whales in the suborder Mysticeti as long ago as the middle Miocene, although it is not known when the members of these families further evolved into their own species.
Recent DNA evidence indicates the fin whale may be more closely related to the humpback whale (Megaptera novaeangliae) and in at least one study the gray whale (Eschrichtius robustus), two whales in different genera, than it is to members of its own genus, such as the minke whales. As of 2006, two subspecies are named, each with distinct physical features and vocalizations. The northern fin whale, B. p. physalus (Linnaeus 1758) inhabits the North Atlantic and the southern fin whale, B. p. quoyi (Fischer 1829) occupies the Southern Ocean. Most experts consider the fin whales of the North Pacific to be a third, as yet unnamed subspecies – this was supported by a 2013 study, which found that the Northern Hemisphere B. p. physalus was not composed of a single subspecies. The three groups mix at most, rarely.
Clarke (2004) proposed a "pygmy" subspecies (B. p. patachonica, Burmeister, 1865) that is purportedly darker in colour and has black baleen. He based this on a single physically mature 19.8 m (65 ft) female caught in the Antarctic in 1947–48, the smaller average size (a few feet) of sexually and physically mature fin whales caught by the Japanese around 50°S, and smaller, darker sexually immature fin whales caught in the Antarctic which he believed were a "migratory phase" of his proposed subspecies. His proposal is not widely accepted and no genetic evidence for their existence is available.
The genetic distance between blue and fin whales has been compared to that between a gorilla and human (3.5 million years on the evolutionary tree.) Nevertheless, hybrid individuals between blue and fin whales with characteristics of both are known to occur with relative frequency in both the North Atlantic and North Pacific.
The fin whale is usually distinguished by its tall spout, long back, prominent dorsal fin, and asymmetrical colouration.
In the Northern Hemisphere, the average size of adult males and females is about 18.5 m (61 ft) and 20 m (66 ft), respectively, averaging 38.5 and 50.5 tonnes (42.5 and 55.5 tons) while in the Southern Hemisphere, it is 20.5 m (67 ft) and 22 m (72 ft), weighing 52.5 and 63 tonnes (58 and 69.5 tons).
In the North Atlantic, the longest reported were a 24.4 m (80 ft) male caught off Shetland in 1905 and a 25 m (82 ft) female caught off Scotland sometime between 1908 and 1914, while the longest reliably measured were three 20.7 m (68 ft) males caught off Iceland in 1973–74 and a 22.5 m (74 ft) female also caught off Iceland in 1975. Mediterranean population are generally smaller, reaching just above 20 m (65.5 ft) at maximum, or may possibly up to 21 m (69 ft) - 23 m (75.5 ft).
In the North Pacific, the longest reported were three 22.9 m (75 ft) males, two caught off California between 1919 and 1926 and the other caught off Alaska in 1925, and a 24.7 m (81 ft) female also caught off California, while the longest reliably measured were a 21 m (69 ft) male caught off British Columbia in 1959 and a 22.9 (75 ft) female caught off central California between 1959 and 1970.
In the Southern Hemisphere, the longest reported for each sex were 25 m (82 ft) and 27.3 m (89.5 ft), while the longest measured by Mackintosh and Wheeler (1929) were 22.65 m (74.5 ft) and 24.53 m (80.5 ft). Major F. A. Spencer, while whaling inspector of the factory ship Southern Princess (1936–38), confirmed the length of a 25.9 m (85.0 ft) female caught in the Antarctic south of the southern Indian Ocean; scientist David Edward Gaskin also measured a 25.9 m (85.0 ft) female while whaling inspector of the British factory ship Southern Venturer in the Southern Ocean in the 1961–62 season. Terence Wise, who worked as a winch operator aboard the British factory ship Balaena, claimed that "the biggest fin [he] ever saw" was a 25.6 m (84.0 ft) specimen caught near Bouvet Island in January 1958. The largest fin whale ever weighed (piecemeal) was a 22.7 m (74.5 ft) pregnant female caught by Japanese whalers in the Antarctic in 1948 which weighed 69.5 tonnes (68.4 long tons; 76.6 short tons), not including 6% for loss of fluids during the flensing process. An individual over 27 m (88.6 ft) is estimated to weigh in excess of 120 tonnes (120 long tons; 130 short tons).
A newborn fin whale measures about 6.0–6.5 m (20–21 ft) in length and weighs about 1,800 kilograms (4,000 lb).
Colouration and markings
The fin whale is brownish to dark or light gray dorsally and white ventrally. The left side of the head is dark gray, while the right side exhibits a complex pattern of contrasting light and dark markings. On the right lower jaw is a white or light gray "right mandible patch", which sometimes extends out as a light "blaze" laterally and dorsally unto the upper jaw and back to just behind the blowholes. Two narrow dark stripes originate from the eye and ear, the former widening into a large dark area on the shoulder — these are separated by a light area called the "interstripe wash". These markings are more prominent on individuals in the North Atlantic than in the North Pacific, where they can appear indistinct. The left side exhibits similar but much fainter markings. Dark, oval-shaped areas of pigment called "flipper shadows" extend below and posterior to the pectoral fins. This type of asymmetry is seen in Omura's whale and occasionally in minke whales. It was thought to have evolved because the whale swims on its right side when surface lunging and it sometimes circles to the right while at the surface above a prey patch. However, the whales just as often circle to the left. No accepted hypothesis explains the asymmetry. It has paired blowholes on a prominent splashguard and a broad, flat, V-shaped rostrum. A single median ridge stops well short of the rostrum tip. A light V-shaped marking, the chevron, begins behind the blowholes and extends back and then forward again. The whale has a series of 56–100 pleats or grooves along the bottom of the body that run from the tip of the chin to the navel that allow the throat area to expand greatly during feeding. It has a curved, prominent dorsal fin that ranges in height from 26–75 cm (10–30 in) (usually 45–60 cm (18–24 in)) and averages about 51 cm (20 in), lying about three-quarters of the way along the back. Its flippers are small and tapered and its tail is wide, pointed at the tip, and notched in the centre.
When the whale surfaces, the dorsal fin is visible soon after the spout. The spout is vertical and narrow and can reach heights of 6 m (20 ft) or more.
Fin whales have very stretchy nerves.
Mating occurs in temperate, low-latitude seas during the winter, followed by an 11- to 12-month gestation period. A newborn weans from its mother at 6 or 7 months of age when it is 11 to 12 m (36 to 39 ft) in length, and the calf accompanies the mother to the summer feeding ground. Females reproduce every 2 or 3 years, with as many as six fetuses being reported, but single births are far more common. Females reach sexual maturity between 6 and 12 years of age at lengths of 17.7–19 m (58–62 ft) in the Northern Hemisphere and 20 m (66 ft) in the Southern Hemisphere.
The fin whale is one of the fastest cetaceans and can sustain speeds between 37 km/h (23 mph) and 41 km/h (25 mph) and bursts up to 46 km/h (29 mph) have been recorded, earning the fin whale the nickname "the greyhound of the sea".
Fin whales are more gregarious than other rorquals, and often live in groups of 6–10, although feeding groups may reach up to 100 animals.
|Multimedia relating to the fin whale
Note that the whale calls have been sped up 10x from their original speed.
Like other whales, males make long, loud, low-frequency sounds. The vocalizations of blue and fin whales are the lowest-frequency sounds made by any animal. Most sounds are frequency-modulated (FM) down-swept infrasonic pulses from 16 to 40 hertz frequency (the range of sounds that most humans can hear falls between 20 hertz and 20 kilohertz). Each sound lasts one to two seconds, and various sound combinations occur in patterned sequences lasting 7 to 15 minutes each. The whale then repeats the sequences in bouts lasting up to many days. The vocal sequences have source levels of up to 184–186 decibels relative to 1 micropascal at a reference distance of one metre and can be detected hundreds of miles from their source.
When fin whale sounds were first recorded by US biologists, they did not realize that these unusually loud, long, pure and regular sounds were being made by whales. They first investigated the possibilities that the sounds were due to equipment malfunction, geophysical phenomena, or even part of a Soviet Union scheme for detecting enemy submarines. Eventually, biologists demonstrated that the sounds were the vocalizations of fin whales.
Direct association of these vocalizations with the reproductive season for the species and that only males make the sounds point to these vocalizations as possible reproductive displays. Over the past 100 years, the dramatic increase in ocean noise from shipping and naval activity may have slowed the recovery of the fin whale population, by impeding communications between males and receptive females.
When feeding, they blow 5–7 times in quick succession, but while traveling or resting will blow once every minute or two. On their terminal (last) dive they arch their back high out of the water, but rarely raise their flukes out of the water. It then dives to depths of up to 470 metres (1,540 ft) when feeding or a few hundred feet when resting or traveling. The average feeding dive off California and Baja lasts 6 minutes, with a maximum of 17 minutes; when traveling or resting they usually dive for only a few minutes at a time.
Range and habitat
Like many large rorquals, the fin whale is a cosmopolitan species. It is found in all the world's major oceans and in waters ranging from the polar to the tropical. It is absent only from waters close to the ice pack at both the north and south extremities and relatively small areas of water away from the large oceans, such as the Red Sea and the Baltic Sea. The highest population density occurs in temperate and cool waters. It is less densely populated in the warmest, equatorial regions.
The North Atlantic fin whale has an extensive distribution, occurring from the Gulf of Mexico and Mediterranean Sea, northward to Baffin Bay and Spitsbergen. In general, fin whales are more common north of approximately 30°N latitude, but considerable confusion arises about their occurrence south of 30°N latitude because of the difficulty in distinguishing fin whales from Bryde's whales. Extensive ship surveys have led researchers to conclude that the summer feeding range of fin whales in the western North Atlantic is mainly between 41°20'N and 51°00'N, from shore seaward to the 1,000 fathoms (1,800 m) contour.
Summer distribution of fin whales in the North Pacific is the immediate offshore waters from central Baja California to Japan and as far north as the Chukchi Sea bordering the Arctic Ocean. They occur in high densities in the northern Gulf of Alaska and southeastern Bering Sea between May and October, with some movement through the Aleutian passes into and out of the Bering Sea. Several whales tagged between November and January off southern California were killed in the summer off central California, Oregon, British Columbia, and in the Gulf of Alaska. Fin whales have been observed feeding 250 miles south of Hawaii in mid-May, and several winter sightings have been made there. Some researchers have suggested that the whales migrate into Hawaiian waters primarily in the autumn and winter.
Although fin whales are certainly migratory, moving seasonally in and out of high-latitude feeding areas, the overall migration pattern is not well understood. Acoustic readings from passive-listening hydrophone arrays indicate a southward migration of the North Atlantic fin whale occurs in the autumn from the Labrador-Newfoundland region, south past Bermuda, and into the West Indies. One or more populations of fin whales are thought to remain year-round in high latitudes, moving offshore, but not southward in late autumn. In the Pacific, migration patterns are poorly characterized. Although some fin whales are apparently present year-round in the Gulf of California, there is a significant increase in their numbers in the winter and spring. Southern fin whales migrate seasonally from relatively high-latitude Antarctic feeding grounds in the summer to low-latitude breeding and calving areas in the winter. The location of winter breeding areas is still unknown, since these whales tend to migrate in the open ocean.
Population and trends
North Atlantic fin whales are defined by the International Whaling Commission to exist in one of seven discrete population zones: Nova Scotia-New England, Newfoundland-Labrador, western Greenland, eastern Greenland-Iceland, North Norway, West Norway-Faroe Islands, and Ireland-Spain-United Kingdom-Portugal. Results of mark-and-recapture surveys have indicated that some movement occurs across the boundaries of these zones, suggesting that they are not entirely discrete and that some immigration and emigration does occur. Sigurjónsson estimated in 1995 that total pre-exploitation population size in the entireNorth Atlantic ranged between 50,000 and 100,000 animals, but his research is criticized for lack of supporting data and an explanation of his reasoning. In 1977, D.E. Sergeant suggested a "primeval" aggregate total of 30,000 to 50,000 throughout the North Atlantic. Of that number, 8,000 to 9,000 would have resided in the Newfoundland and Nova Scotia areas, with whales summering in U.S. waters south of Nova Scotia presumably omitted. J.M. Breiwick estimated that the "exploitable" (above the legal size limit of 50 ft) component of the Nova Scotia population was 1,500 to 1,600 animals in 1964, reduced to only about 325 in 1973. Two aerial surveys in Canadian waters since the early 1970s gave numbers of 79 to 926 whales on the eastern Newfoundland-Labrador shelf in August 1980, and a few hundred in the northern and central Gulf of Saint Lawrence in August 1995 – 1996. Summer estimates in the waters off western Greenland range between 500 and 2,000, and in 1974, Jonsgard considered the fin whales off Western Norway and the Faroe Islands to "have been considerably depleted in postwar years, probably by overexploitation". The population around Iceland appears to have fared much better, and in 1981, appeared to have undergone only a minor decline since the early 1960s. Surveys during the summers of 1987 and 1989 estimated of 10,000 to 11,000 between eastern Greenland and Norway. This shows a substantial recovery when compared to a survey in 1976 showing an estimate of 6,900, which was considered to be a "slight" decline since 1948. A Spanish NASS survey in 1989 of the France-Portugal-Spain sub-area estimated a summer population range at 17,355. The aggregate population level in the Mediterranean basin is estimated to be between 40,000 and 56,000 individuals. Satellite tracking revealed that those found in Pelagos Sanctuary migrate southward to off Tunisia, Malta, Pantelleria, and Sicily, and also possibly winter off coastal southern Italy, Sardinia, within the Strait of Messina, Aeolian Islands, and off Libya, Kerkennah Islands, Lampedusa, and whales may recolonize out of the Ligurian Sea to other areas such as in Ionian and in Adriatic Sea. Biology of the species along southern and southeastern parts of the basin such as off Libya, Algeria, and northern Egypt, is unclear due to lacks of scientific approaches although whales have been confirmed off the furthermost of the basin such as along Levantine Sea including Israel, Lebanon, and Cyprus. Documented records within Turkish waters have been in very small numbers; one sighting off Antalya in 1994 and 5 documented strandings as of 2016.
The total historical North Pacific population was estimated at 42,000 to 45,000 before the start of whaling. Of this, the population in the eastern portion of the North Pacific was estimated to be 25,000 to 27,000. By 1975, the estimate had declined to between 8,000 and 16,000. Surveys conducted in 1991, 1993, 1996, and 2001 produced estimates between 1,600 and 3,200 off California and 280 and 380 off Oregon and Washington. The minimum estimate for the California-Oregon-Washington population, as defined in the U.S. Pacific Marine Mammal Stock Assessments: 2005, is about 2,500. Surveys in coastal waters of British Columbia in summers 2004 and 2005 produced abundance estimates of approximately 500 animals. Surveys near the Pribilof Islands in the Bering Sea indicated a substantial increase in the local abundance of fin whales between 1975–1978 and 1987–1989. In 1984, the entire population was estimated to be less than 38% of its historic carrying capacity. Fin whales might have started returning to the coastal waters off British Columbia (a sighting occurred in Johnstone Strait in 2011) and Kodiak Island. Size of the local population migrating to Hawaiian Archipelago is unknown. Historically, several other wintering grounds were scattered in the North Pacific in the past, such as off the Northern Mariana Islands, Bonin Islands, and Ryukyu Islands (for other possible habitats, see blue whale as their habitat preferences may correspond).
For Asian stocks, resident groups may exist in the Yellow Sea and East China Sea, and the Sea of Japan (though these populations are critically endangered and the population off China, Korea, and Japan are either near extinction or in very small numbers). Very small increases in sightings have been confirmed off Shiretoko Peninsula, Abashiri, and Kushiro in Hokkaido, Tsushima, Sado Island, off Maiduru in the Sea of Japan since in late 2000s as whales in Sea of Okhotsk might have started recolonizing into former habitats (for coastal Sakhalin, as well). Whales possibly used to migrated into Seto Inland Sea.
Studies of historical catches suggest several resident groups once existed in the North Pacific - the Baja California group and the Yellow Sea–East China Sea (including Ryukyu Islands and western Kyusyu) group. Additionally, respective groups in northern Sea of Japan and the group along Pacific coasts of Japan from Hokkaido to Sanriku might have been resident or less migratory, as well. Recent sightings of large whales exceeding 20 m in length, likely to be fin whales, as blue whales in coastal northeast Asia are considered to be extinct, indicate that remnants of the Sea of Japan or the Yellow– ohai Sea groups still pass through the Tsushima Strait where all the larger cetaceans are under threats of being struck by high-speed vessels. Southward migrations to Taiwan or East and South China Seas may still occur, but the whole scale of current migrations along Eurasian continent including population size is unclear. The only modern record among Ryukyu Islands was of a rotten carcass beached on Ishigaki Island in 2005.
There had been congregation areas among Sea of Japan to Yellow Sea such as in East Korea Bay, along eastern coasts of Korean Peninsula, and Ulleungdo, although recent occurrences into these locations are of unclear due to locational disorders.
- Fin whales in Yellow Sea could have been a unique form from outer Pacific populations due to their smaller size of around 20m or more at near maximum, and breeding season in these regions was mainly in winter.
Modern sightings around Commander Islands have been annual but not in great numbers, and whales likely to migrate through the areas rather than summering. Possibilities of whales seen in Commander Islands might mix with other populations among Asian and eastern Pacific populations has been considered.
Very little information has been revealed about the ecology of current migration from Antarctic waters are unknown, but small increases in sighting rates are confirmed off New Zealand, such as off Kaikoura, and wintering grounds may exist in further north such as in Papua New Guinea, Fiji, and off East Timor. Confirmations in Rarotonga have been increased recently where interactions with humpback whales occur on occasions. Finbacks are also relatively abundant along the coast of Peru and Chile (in Chile, most notably off Los Lagos region such as Gulf of Corcovado in Chiloé National Park, Punta de Choros, port of Mejillones, and Caleta Zorra. Year-round confirmations indicate possible residents off pelagic north eastern to central Chile such as around coastal Caleta Chañaral and Pingüino de Humboldt National Reserve, east of Juan Fernández Islands, and northeast of Easter Island and possible wintering ground exist for eastern south Pacific population. They are known to make mixed groups with other rorquals such as blue whales and sei whales. Their recovery is confirmed vicinity to various subantarctic islands such as South Georgia and Falkland, but unknown in other historical habitats including Campbell Island, Kermadec to Chatham Islands, Tristan da Cunha, and Gough Island.
Relatively little is known about the historical and current population levels of the Southern fin whale. The IWC officially estimates that the Southern Hemisphere pre-whaling population was 400,000 whales and that the population in 1979 (at the cessation of Antarctic large scale whaling) was 85,200. Both the current and historical estimates should be considered as poor estimates because the methodology and data used in the study are known to be flawed. Other estimates cite current size to be between 15,000 (1983) and 38,000 (1997). As of 2006, there is no scientifically accepted estimate of current population or trends in abundance.
The only known predator of the fin whale is the killer whale, with at least 20 eyewitness and second-hand accounts of attack or harassment. They usually flee and offer little resistance to attack. Only a few confirmed fatalities have occurred. In October 2005, 16 killer whales attacked and killed a fin whale in the Canal de Ballenas, Gulf of California, after chasing it for about an hour. They fed on its sinking carcass for about 15 minutes before leaving the area. In June 2012, a pod of killer whales was seen in La Paz Bay, in the Gulf of California, chasing a fin whale for over an hour before finally killing it and feeding on its carcass. The whale bore numerous tooth rakes over its back and dorsal fin; several killer whales flanked it on either side, with one individual visible under water biting at its right lower jaw. In July 1908, a whaler reportedly saw two killer whales attack and kill a fin whale off western Greenland. In January 1984, seven were seen from the air circling, holding the flippers, and ramming a fin whale in the Gulf of California, but the observation ended at nightfall.
In the North Pacific, they feed on euphausiids in the genera Euphausia, Thysanoessa, and Nyctiphanes, large copepods in the genus Neocalanus, small schooling fish (e.g. the genera Engraulis, Mallotus, Clupea, and Theragra), and squid. Based on stomach content analysis of over 19,500 fin whales caught by the Japanese whaling fleet in the North Pacific from 1952 to 1971, 64.1% contained only krill, 25.5% copepods, 5.0% fish, 3.4% krill and copepods and 1.7% squid. Nemoto (1959) analysed the stomach contents of about 7500 fin whales caught in the northern North Pacific and Bering Sea from 1952 to 1958, found that they mainly preyed on euphausiids around the Aleutian Islands and in the Gulf of Alaska and schooling fish in the northern Bering Sea and off Kamchatka. In the northern Bering Sea (north of 58°N), their main prey species were capelin (Mallotus villosus), Alaska pollock (Theragra chalcogramma) and Pacific herring (Clupea pallasii); they also consumed saffron cod (Eleginus gracilis). Arctic krill (Thysanoessa raschii) was the only species of euphausiid found in the stomachs of fin whales in the northern Bering Sea. Off Kamchatka, they appeared to primarily feed on herring. They also took large quantities of the copepod Neocalanus cristatus around the Aleutian Islands and in Olyutorsky Bay off northeast Kamchatka, areas where the species was abundant. Five species of euphausiid (Euphausia pacifica, Thysanoessa spinifera, T. inermis, T. raschii, and T. longipes) were the predominant prey around the Aleutian Islands and in the Gulf of Alaska. Prey varied by region in the Kuril Islands area, with euphausiids (T. longipes, T. inermis, and T. raschii) and copepods (Neocalanus plumchrus and N. cristatus) being the main prey in the northern area and Japanese flying squid (Todarodes pacificus pacificus) and small schooling fish (e.g. Pacific saury, Cololabis saira; and Japanese anchovy, Engraulis japonicus) dominating the diet in the southern area.
Of the fin whale stomachs sampled off British Columbia between 1963 and 1967, euphausiids dominated the diet for four of the five years (82.3 to 100% of the diet), while copepods only formed a major portion of the diet in 1965 (35.7%). Miscellaneous fish, squid, and octopus played only a very minor part of the diet in two of the five years (3.6 to 4.8%). Fin whales caught off California between 1959 and 1970 fed on the pelagic euphausiid Euphausia pacifica (86% of sampled individuals), the more neritic euphausiid Thysanoessa spinifera (9%), and the northern anchovy (Engraulis mordax) (7%); only trace amounts (<0.5% each) were found of Pacific saury (C. saira) and juvenile rockfish (Sebastes jordani). In the Gulf of California, they have been observed feeding on swarms of the euphausiid Nyctiphanes simplex.
In the North Atlantic, they prey on euphausiids in the genera Meganyctiphanes, Thysanoessa and Nyctiphanes and small schooling fish (e.g. the genera Clupea, Mallotus, and Ammodytes). Of the 1,609 fin whale stomachs examined at the Hvalfjörður whaling station in southwestern Iceland from 1967 to 1989 (caught between June and September), 96% contained only krill, 2.5% krill and fish, 0.8% some fish remains, 0.7% capelin (M. villosus), and 0.1% sandeel (family Ammodytidae); a small proportion of (mainly juvenile) blue whiting (Micromesistius poutassou) were also found. Of the krill sampled between 1979 and 1989, the vast majority (over 99%) was northern krill (Meganyctiphanes norvegica); only one stomach contained Thysanoessa longicaudata. Off West Greenland, 75% of the fin whales caught between July and October had consumed krill (family Euphausiidae), 17% capelin (Mallotus) and 8% sand lance (Ammodytes sp.). Off eastern Newfoundland, they chiefly feed on capelin, but also take small quantities of euphausiids (mostly T. raschii and T. inermis). In the Ligurian-Corsican-Provençal Basin in the Mediterranean Sea they make dives as deep as 470 metres (1,540 ft) to feed on the euphausiid Meganyctiphanes norvegica, while off the island of Lampedusa, between Tunisia and Sicily, they have been observed in mid-winter feeding on surface swarms of the small euphausiid Nyctiphanes couchi.
In the Southern Hemisphere, they feed almost exclusively on euphausiids (mainly the genera Euphausia and Thysanoessa), as well as taking small amounts of amphipods (e.g. Themisto gaudichaudii) and various species of fish. Of the more than 16,000 fin whales caught by the Japanese whaling fleet in the Southern Hemisphere between 1961 and 1965 that contained food in their stomachs, 99.4% fed on euphausiids, 0.5% on fish, and 0.1% on amphipods. In the Southern Ocean they mainly consume E. superba.
The animal feeds by opening its jaws while swimming at some 11 kilometres per hour (6.8 mph) in one study, which causes it to engulf up to 70 cubic metres (18,000 US gal; 15,000 imp gal) of water in one gulp. It then closes its jaws and pushes the water back out of its mouth through its baleen, which allows the water to leave while trapping the prey. An adult has between 262 and 473 baleen plates on each side of the mouth. Each plate is made of keratin that frays out into fine hairs on the ends inside the mouth near the tongue. Each plate can measure up to 76 centimetres (30 in) in length and 30 centimetres (12 in) in width.
The whale routinely dives to depths of more than 200 metres (660 ft) where it executes an average of four "lunges", to accumulate krill. Each gulp provides the whale with approximately 10 kilograms (22 lb) of food. One whale can consume up to 1,800 kilograms (4,000 lb) of food a day, leading scientists to conclude that the whale spends about three hours a day feeding to meet its energy requirements, roughly the same as humans. If prey patches are not sufficiently dense, or are located too deep in the water, the whale has to spend a larger portion of its day searching for food. One hunting technique is to circle schools of fish at high speed, frightening the fish into a tight ball, then turning on its side before engulfing the massed prey.
Fin whales suffer from a number of pathological conditions. The parasitic copepod Pennella balaenopterae—usually found on the flank of fin whales—burrows into their blubber to feed on their blood, while the pseudo-stalked barnacle Xenobalanus globicipitis is generally found more often on the dorsal fin, pectoral fins, and flukes.
Other barnacles found on fin whales include the acorn barnacle Coronula reginae and the stalked barnacle Conchoderma auritum, which attaches to Coronula or the baleen. The harpacticid copepod Balaenophilus unisetus (heavy infestations of which have been found in fin whales caught off northwestern Spain) and the ciliate Haematophagus also infest the baleen, the former feeding on the baleen itself and the latter on red blood cells.
The remora Remora australis and occasionally the amphipod Cyamus balaenopterae can also be found on fin whales, both feeding on the skin. Infestations of the giant nematode Crassicauda boopis can cause inflammation of the renal arteries and potential kidney failure, while the smaller C. crassicauda infects the lower urinary tract.
An emaciated 13 m (43 ft) female fin whale, which stranded along the Belgian coast in 1997, was found to be infected with lesions of Morbillivirus. In January 2011, a 16.7 m (55 ft) emaciated adult male fin whale stranded dead on the Tyrrhenian coastline of Italy was found to be infected with Morbillivirus and the protozoa Toxoplasma gondii, as well as carrying heavy loads of organochlorine pollutants.
In the 19th century, the fin whale was occasionally hunted by open-boat whalers, but it was relatively safe, because it could easily outrun ships of the time and often sank when killed, making the pursuit a waste of time for whalers. However, the later introduction of steam-powered boats and harpoons that exploded on impact made it possible to kill and secure them along with blue and sei whales on an industrial scale. As other whale species became overhunted, the whaling industry turned to the still-abundant fin whale as a substitute. It was primarily hunted for its blubber, oil, and baleen. Around 704,000 fin whales were caught in Antarctic whaling operations alone between 1904 and 1975.
The introduction of factory ships with stern slipways in 1925 substantially increased the number of whales taken per year. In 1937–38 alone, over 29,000 fin whales were taken. From 1953–54 to 1961–62, the catch averaged over 30,000 per year. By 1962–63, sei whale catches began to increase as fin whales became scarce. By 1975–76, fewer than 1,000 fin whales were being caught each year. In the North Pacific, over 74,000 fin whales were caught between 1910 and 1975. Between 1910 and 1989, over 55,000 were caught in the North Atlantic. Coastal groups in northeast Asian waters, along with many other baleen species, were likely driven into serious perils or functional extinctions by industrial catches by Japan covering wide ranges of China and Korean EEZ within very short period in 20th century. Migrations of the species into Japanese EEZ and in East China Sea were likely to be exterminated relatively earlier, as the last catch records on Amami Oshima was between the 1910s and 1930s. After the cease of exploiting Asian stocks, Japan kept mass commercial and illegal hunts until 1975. Several thousand individuals were hunted from various stations mainly along coasts of Hokkaido, Sanriku, and the Gotō Islands.
The IWC prohibited hunting in the Southern Hemisphere in 1976. The Soviet Union engaged in the illegal killing of protected whale species in the North Pacific and Southern Hemisphere, over-reporting fin whale catches to cover up illegal takes of other species. In the North Pacific, they reported taking over 10,000 fin whales between 1961–79, while the true catch was less than 9,000. In the Southern Hemisphere, they reported taking nearly 53,000 between 1948 and 1973, when the true total was a little over 41,000. The fin whale was given full protection from commercial whaling by the IWC in the North Pacific in 1976, and in the North Atlantic in 1987, with small exceptions for aboriginal catches and catches for research purposes. All populations worldwide remain listed as endangered species by the US National Marine Fisheries Service and the International Conservation Union Red List. The fin whale is on Appendix 1 of CITES.
The IWC has set a quota of 19 fin whales per year for Greenland. Meat and other products from whales killed in these hunts are widely marketed within Greenland, but export is illegal. Iceland and Norway are not bound by the IWC's moratorium on commercial whaling because both countries filed objections to it.
In October 2006, Iceland's fisheries ministry authorized the hunting of 9 fin whales through August 2007. In 2009 and 2010, Iceland caught 125 and 148 fin whales, respectively. An Icelandic company, Hvalur, caught over a hundred fin whales in 2014, and exported a record quantity of 2071 tonnes in a single shipment in 2014. Since 2006, Hvalur has caught more than 500 fin whales and exported more than 5000 tonnes of whale meat to Japan.
In the Southern Hemisphere, Japan permits annual takes of 10 fin whales under its Antarctic Special Permit whaling program for the 2005–2006 and 2006–2007 seasons. The proposal for 2007–2008 and the subsequent 12 seasons allows taking 50 per year. While 10 fin whales were caught in the 2005–06 season and three in the 2006–07 season, none was caught in the 2007–2008 season. A single fin whale was caught in both the 2008–09 and 2009–10 seasons, two were taken in the 2010–11 season, and one was taken in the 2011–12 season.
Not only humpback, minkes, sperm, and many other smaller Odontoceti, but also including critically endangered species such as North Pacific right, western gray, and Northern fin whales have been targets of illegal captures using harpoons for dolphin hunts or intentionally drive whales into nets, and later reports to administrative organs or research institutions as cases of 'entanglements where fishermen tried their best to save whales'. Protected species' meats can also be found on markets even today which are mostly "byproducts" of entanglements, and one case scientifically revealed that at least some humpbacks with other species were illegally hunted in EEZ of antiwhaling nations such as off Mexico or South Africa, and tried to import into Japan by hiring vessels from other countries and even trying to go on overland routes within other nations.
Collisions with ships are a major cause of mortality. In some areas, they cause a substantial portion of large whale strandings. Most serious injuries are caused by large, fast-moving ships over or near continental shelves.
A 60-ft-long fin whale was found stuck on the bow of a container ship in New York harbor on 12 April 2014.
Ship collisions frequently occur in Tsushima Strait and result in damaging all of whales, passengers, and vessels, hence the Japanese Coast Guard has started visual recordings of large cetaceans in Tsushima Strait to inform operating vessels in the areas.
Several fin whale skeletons are exhibited in North America. The Natural History Museum of Los Angeles County in Los Angeles, California has an exhibit entitled the "Fin Whale Passage", which displays a 19.2 m (63 ft) fin whale skeleton collected by former museum osteologist Eugene Fischer and field collector Howard Hill in 1926 from the Trinidad whaling station (1920–1926) in Humboldt County, northern California. A steel armature supports the skeleton, which is accompanied by sculpted flukes. Science North, a science museum in Greater Sudbury, Ontario, Canada, has a 20 m (66 ft) fin whale skeleton collected from Anticosti Island hanging from the fourth floor of its main building. The Grand Rapids Public Museum in Grand Rapids, Michigan contains a 76-ft-long skeleton in the Galleria section hanging above from the ceiling.
Several fin whale skeletons are also exhibited in Europe. The Natural History Museum of Slovenia in Ljubljana, Slovenia, houses a 13 m (43 ft) female fin whale skeleton – the specimen had been found floating in the Gulf of Piran in the spring of 2003. The Hungarian Natural History Museum in Budapest, Hungary, displays a fin whale skeleton hanging near its main entrance which had been caught in the Atlantic Ocean in 1896 and purchased from Vienna in 1900. The Cambridge University Museum of Zoology, in Cambridge, United Kingdom, exhibits a nearly 21 m (69 ft) male fin whale skeleton, which had stranded at Pevensey, East Sussex, in November 1865.
Fin whales are regularly encountered on whale-watching excursions worldwide. In the Southern California Bight, fin whales are encountered year-round, with the best sightings between November and March. They can even be seen from land (for example, from Point Vicente, Palos Verdes, where they can be seen lunge feeding at the surface only a half mile to a few miles offshore). They are regularly sighted in the summer and fall in the Gulf of St. Lawrence, the Gulf of Maine, the Bay of Fundy, the Bay of Biscay, Strait of Gibraltar, the Mediterranean. In southern Ireland, they are seen inshore from June to February, with peak sightings in November and December. Cruise ships en route to and from the Antarctic Peninsula sometimes encounter fin whales in the Drake Passage.
The fin whale is listed on both Appendix I and Appendix II of the Convention on the Conservation of Migratory Species of Wild Animals (CMS). It is listed on Appendix I as this species has been categorized as in danger of extinction throughout all or a significant proportion of its range and CMS Parties strive towards strictly protecting these animals, conserving or restoring the places where they live, mitigating obstacles to migration and controlling other factors that might endanger them.
It is listed on Appendix II as it has an unfavourable conservation status or would benefit significantly from international co-operation organised by tailored agreements. In addition, the fin whale is covered by the Agreement on the Conservation of Cetaceans in the Black Sea, Mediterranean Sea and Contiguous Atlantic Area (ACCOBAMS) and the Memorandum of Understanding for the Conservation of Cetaceans and Their Habitats in the Pacific Islands Region (Pacific Cetaceans MOU).
- The use of Order Cetartiodactyla, instead of Cetacea with Suborders Odontoceti and Mysticeti, is favored by most evolutionary mammalogists working with molecular data  and is supported the IUCN Cetacean Specialist Group and by Taxonomy Committee  of the Society for Marine Mammalogy, the largest international association of marine mammal scientists in the world. See Cetartiodactyla and Marine mammal articles for further discussion.
- Mead, J.G.; Brownell, R. L. Jr. (2005). "Order Cetacea". In Wilson, D.E.; Reeder, D.M. Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Johns Hopkins University Press. p. 725. ISBN 978-0-8018-8221-0. OCLC 62265494.
- Reilly, S.B., Bannister, J.L., Best, P.B., Brown, M., Brownell Jr., R.L., Butterworth, D.S., Clapham, P.J., Cooke, J., Donovan, G.P., Urbán, J. & Zerbini, A.N. (2008). Balaenoptera physalus. In: IUCN 2008. IUCN Red List of Threatened Species. Retrieved 7 October 2008.
- Agnarsson, I.; May-Collado, LJ. (2008). "The phylogeny of Cetartiodactyla: the importance of dense taxon sampling, missing data, and the remarkable promise of cytochrome b to provide reliable species-level phylogenies". Mol Phylogenet Evol. 48 (3): 964–985. doi:10.1016/j.ympev.2008.05.046. PMID 18590827.
- Price, SA.; Bininda-Emonds, OR.; Gittleman, JL. (2005). "A complete phylogeny of the whales, dolphins and even-toed hoofed mammals – Cetartiodactyla". Biol Rev Camb Philos Soc. 80 (3): 445–473. doi:10.1017/s1464793105006743. PMID 16094808.
- Montgelard, C.; Catzeflis, FM.; Douzery, E. (1997). "Phylogenetic relationships of artiodactyls and cetaceans as deduced from the comparison of cytochrome b and 12S RNA mitochondrial sequences". Molecular Biology and Evolution. 14 (5): 550–559. doi:10.1093/oxfordjournals.molbev.a025792. PMID 9159933.
- Spaulding, M.; O'Leary, MA.; Gatesy, J. (2009). "Relationships of Cetacea -Artiodactyla- Among Mammals: Increased Taxon Sampling Alters Interpretations of Key Fossils and Character Evolution". PLoS ONE. 4 (9): e7062. Bibcode:2009PLoSO...4.7062S. doi:10.1371/journal.pone.0007062. PMC . PMID 19774069.
- Cetacean Species and Taxonomy. iucn-csg.org
- The Society for Marine Mammalogy's Taxonomy Committee List of Species and subspecies Archived 6 January 2015 at the Wayback Machine..
- Synopsis Mammalium. 1829. p. 525.
- Hist. Nat. Gén. et Partie, des Mamm. et Oiseaux découverts depuis 1788
- Nat. Hist. Cetacea
- Bulletins de l'Académie Royale des Sciences, des Lettres et des Beaux-Arts ... – Académie Royale des Sciences, des Lettres et des Beaux-Arts de Belgique (Bruxelles) – Google ubNX. 1859. p. 403.
- "Balaenoptera physalus Fin Whale". MarineBio.org. Retrieved 23 October 2006.
- Mackintosh, N. A.; Wheeler, J. F. G. (1929). "Southern blue and fin whales". Discovery Reports. I: 259–540.
- Mackintosh, N. A. (1943). "The southern stocks of whalebone whales". Discovery Reports. XXII: 199–300.
- Lockyer, C. (1976) Body weights of some species of large whales. J. Cons. int. Explor. Mer, 36 (3); 259–273.
- Andrews, Roy Chapman. (1916). Whale hunting with gun and camera; a naturalist's account of the modern shore-whaling industry, of whales and their habits, and of hunting experiences in various parts of the world. New York: D. Appleton and Co., p. 158.
- National Marine Fisheries Service (2006). Draft recovery plan for the fin whale (Balaenoptera physalus) (PDF). Silver Spring, Maryland: National Marine Fisheries Service.
- "Revised Management Scheme". International Whaling Commission. Retrieved 7 November 2006.
- Shirihai, H.; Jarrett, B. (2006). Whales, Dolphins and Other Marine Mammals of the World. Princeton Field Guides. pp. 43–45. ISBN 0691127573.
- (Latin) Linnaeus, C (1758). Systema naturae per regna tria naturae, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Tomus I. Editio decima, reformata. Holmiae. (Laurentii Salvii). p. 824.
- Allen, G. M. (1915). The Whalebone whales of New England. pp. 176–78.
- Cousteau, Jacques (1988). Whales. p. 77.
- Gingerich, P. (2004). "Whale Evolution". McGraw-Hill Yearbook of Science & Technology. The McGraw Hill Companies. ISBN 0-07-142784-8.
- Arnason, U.; Gullberg A. & Widegren, B. (1 September 1993). "Cetacean mitochondrial DNA control region: sequences of all extant baleen whales and two sperm whale species". Molecular Biology and Evolution. 10 (5): 960–970. PMID 8412655. Retrieved 25 January 2009.
- Sasaki, T.; et al. (23 February 2005). "Mitochondrial Phylogenetics and Evolution of Mysticete Whales". Systematic Biology. 54 (1): 77–90. doi:10.1080/10635150590905939. PMID 15805012. Retrieved 25 January 2009.
- Hatch, L.T., Dopman, E.B. & Harrison, R.G. (26 May 2006). "Phylogenetic relationships among the baleen whales based on maternally and paternally inherited characters" (PDF). Molecular Phylogenetics and Evolution. 41 (1): 12–27. doi:10.1016/j.ympev.2006.05.023.
- "Balaenoptera physalus". Integrated Taxonomic Information System. Retrieved 23 October 2006.
- Archer, FI; Morin, PA; Hancock-Hanser, BL; Robertson, KM; Leslie, MS; et al. (2013). "Mitogenomic Phylogenetics of Fin Whales (Balaenoptera physalus spp.): Genetic Evidence for Revision of Subspecies". PLoS ONE. 8 (5): e63396. Bibcode:2013PLoSO...863396A. doi:10.1371/journal.pone.0063396.
- Clarke, R. (2004). "Pygmy fin whales". Marine Mammal Science. 20 (2): 329–334. doi:10.1111/j.1748-7692.2004.tb01161.x.
- A. Arnason; A. Gullberg (1993). "Comparison between the complete mtDNA sequences of the blue and fin whale, two species that can hybridize in nature". Journal of Molecular Ecology. 37 (4): 312–322. PMID 8308901.
- Árnasson, Ú; Spilliaert, R; Pálsdóttir, Á; Árnasson, Ú (January 1998). "A new hybrid between a blue whale, Balaenoptera musculus, and a fin whale, B. physalus: frequency and implications of hybridization". Marine Mammal Science. 14 (1): 82–98. doi:10.1111/j.1748-7692.1998.tb00692.x.
- Bérubé, Martine; Aguilar, Alex (1998). "A new hybrid between a blue whale, Balaenoptera musculus, and a fin whale, B. physalus: frequency and implications of hybridization". Marine Mammal Science. 14 (1): 82–98. doi:10.1111/j.1748-7692.1998.tb00692.x.
- Doroshenko, V.N. (1970). "A whale with features of the fin and blue whale (in Russian)". Izvestia TINRO. 70: 225–257.
- Palumbi, S.R.; Cipriano, F. (1998). "Species Identification Using Genetic Tools: The Value of Nuclear and Mitochondrial Gene Sequences in Whale Conservation" (PDF). Journal of Heredity. 89 (5): 459–. doi:10.1093/jhered/89.5.459. PMID 9768497.
- Ogino M. (2005)『クジラの死体はかく語る』, Kodansha
- Evans, Peter G. H. (1987). The Natural History of Whales and Dolphins. Facts on File.
- Haldane, R.C. (January 1906). Whaling in Scotland. Ann. Scot. Nat. His., No. 57, p. 131.
- Thompson, D'Arcy Wentworth. (Jan.-Feb. 1919). On whales landed at the Scottish whaling stations, especially during the years 1908–1914—Parts IV. to VI. The bottlenose, humpback, and finner whales. The Scottish Naturalist, Nos. 85–86, pp. 6–16.
- Lockyer, C.; Brown, S. G. (1979). "A review of recent biological data for the fin whale population off Iceland". Rep. int. Whal. Commn. 29: 185–9.
- Lockyer, C.; Gambell, R.; Brown, S. G. (1977). "Notes on age data of fin whales taken off Iceland, 1967–74". Rep. int. Whal. Commn. 27: 427–50.
- Fin whale - Ionian Dolphin Project
- Clapham; et al. (1997). "Catches of Humpback and Other Whales from Shore Stations at Moss Landing and Trinidad, California, 1919–1926". Mar Mam. Sci. 13 (3): 368–94. doi:10.1111/j.1748-7692.1997.tb00646.x.
- Reeves, R.R.; Leatherwood, S.; Karl, S.A.; Yohe, E.R. (1985). "Whaling results at Akuktan (1912–39) and Port Hobron (1926–37), Alaska". Rep. int. Whal. Commn. 35: 441–457.
- Nichol, L. and K. Heise. (1992). The historical occurrence of large whales off the Queen Charlotte Islands. Prep. for South Moresby/Gwaii Haanas National Parks Reserve, Canadian Parks Service, Queen Charlotte City, B.C. 68 pp.
- Gaskin, D. E. (1968). "The New Zealand Cetacea".Fish. Res. Bull., N.Z. (n.s.) 1: 1–92.
- Wise, Terence. 1970. To Catch a Whale. Geoffrey Bles.
- Fox, David (2001). "Balaenoptera physalus (fin whale)". Animal Diversity Web. Retrieved 22 October 2006.
- Tershy, B. R.; D. Wiley (1992). "Asymmetrical pigmentation in the fin whale: a test of two feeding related hypotheses". Marine Mammal Science. 8 (3): 315–318. doi:10.1111/j.1748-7692.1992.tb00416.x.
- Robert Shadwick (reported by Edward Yong) (2015).Giant Whales Have Super-Stretchy Nerves, National Geographic & A Coghlan : DOI: 10.1016/j.cub.2015.03.007 [Retrieved 2015-05-08]
- Martin, Anthony R. (1991). Whales and dolphins. London: Salamander Books. ISBN 0-8160-3922-4.
- Ditte Haue. "Finhvalen var mindst 135 år gammel | Nyheder | DR". Dr.dk. Retrieved 13 May 2013.
- "Fin Whale". nature.ca: Canadian Museum of Nature. Retrieved 22 October 2006.
- Payne, Roger (1995). Among Whales. New York: Scribner. p. 176. ISBN 0-684-80210-4.
- "Finback Whales". Bioacoustics Research Program, Cornell Lab of Ornithology. Retrieved 26 October 2006.
- W. J. Richardson, C. R. Greene, C. I. Malme and D. H. Thomson, Marine Mammals and Noise (Academic Press, San Diego, 1995).
- Croll, D.A.; Clark, C.W.; Acevedo, A.; Flores, S.; Gedamke, J.; Urban, J.; Urban, Jorge (2002). "Only male fin whales sing loud songs" (PDF). Nature. 417 (6891): 809. Bibcode:2002Natur.417..809C. doi:10.1038/417809a.
- Watkins, W.; Tyack, P.; Moore, K.; Bird, J. (1987). "The 20 Hz signals of finback whales (Balaenoptera physalus)". The Journal of the Acoustical Society of America. 82 (6): 1901–1902. Bibcode:1987ASAJ...82.1901W. doi:10.1121/1.395685.
- Segelken, R. (19 June 2002). "Humanity's din in the oceans could be blocking whales' courtship songs and population recovery". Cornell University. Retrieved 11 November 2006.
- Croll, D. A.; Acevedo-Gutiérrez, A.; Tershy, B.R.; Urbán-Ramírez, J. (2001). "The diving behavior of blue and fin whales: is dive duration shorter than expected based on oxygen stores?" (PDF). Comp Biochem Physiol A. 129 (4): 797–809. doi:10.1016/s1095-6433(01)00348-8.
- Mead, J.G. (1977). "Records of Sei and Bryde's whales from the Atlantic Coast of the United States, the Gulf of Mexico, and the Caribbean". Rep. Int. Whal. Commn. Spec. Iss. 1: 113–116. ISBN 0-906975-03-4.
- Mitchell, E. (1974). "Present status of Northwest Atlantic fin and other whale stocks". In W.E. Schevill. The Whale Problem: A Status Report. Cambridge, MA: Harvard University Press. pp. 108–169. ISBN 0-674-95075-5.
- Rice, D.W. (1974). "Whales and whale research in the eastern North Pacific". In W.E. Schevill. The Whale Problem: A Status Report. Cambridge, MA: Harvard University Press. pp. 170–195. ISBN 0-674-95075-5.
- Reeves, R.R.; M.W. Brown (1985). "Whaling in the Bay of Fundy". Whalewatcher. 19 (4): 14–18.
- Mobley, J.R. Jr.; M. Smultea, T. Norris and D. Weller (1996). "Fin whale sighting north of Kaua'i, Hawai'i". Pacific Science. 50 (2): 230–233.
- Thompson, P.O.; W.A. Friedl (1982). "A long term study of low frequency sound from several species of whales off Oahu, Hawaii". Cetology. 45: 1–19.
- Clark, C.W. (1995). "Application of US Navy underwater hydrophone arrays for scientific research on whales". Rep. Int. Whal. Commn. 45: 210–212.
- Tershy, B.R.; D. Breese and C.S. Strong (1990). "Abundance, seasonal distribution and population composition of balaenopterid whales in the Canal de Ballenas, Gulf of California, Mexico". Rep. Int. Whal. Commn. Spec. Iss. 12: 369–375. ISBN 0-906975-23-9.
- Sigurjónsson, J. (1995). "On the life history and autecology of North Atlantic rorquals". In A.S. Blix; L. Walløe; Ø. Ulltang. Whales, Seals, Fish and Man. Elsevier Science. pp. 425–441. ISBN 0-444-82070-1.
- D.E. Sergeant (1977). "Stocks of fin whales Balaenoptera physalusL. in the North Atlantic Ocean". Rep. Int. Whal. Commn. 27: 460–473.
- Allen, K.R. (1970). "A note on baleen whale stocks of the north west Atlantic". Rep. Int. Whal. Commn. 20: 112–113.
- Breiwick, J.M. (1993). "Population dymanics and analyses of the fisheries for fin whales (Balaenoptera physalus) in the northwest Atlantic Ocean". (Ph.D. thesis) University of Washington, Seattle. 310 pp.
- Hay, K. (1982). "Aerial line-transect estimates of abundance of humpback, fin, and long-finned pilot whales in the Newfoundland-Labrador area". Rep. Int. Whal. Commn. 31: 373–387.
- Kingsley, M.C.S.; R.R. Reeves (1998). "Aerial surveys of cetaceans in the Gulf of St. Lawrence in 1995 and 1996". Marine Mammal Science. 17 (1): 35–75. doi:10.1139/cjz-76-8-1529.
- Larsen, F. (1995). "Abundance of minke and fin whales off West Greenland". Rep. Int. Whal. Commn. 45: 365–370.
- Jonsgard, A. (1974). "On whale exploitation in the eastern part of the North Atlantic Ocean". In W.E. Schevill. The Whale Problem: A Status Report. Cambridge, MA: Harvard University Press. pp. 97–107. ISBN 0-674-95075-5.
- Rørvik, C.J.; J. Sigurjónsson (1981). "A note on the catch per unit effort in the Icelandic fin whale fishery". Rep. Int. Whal. Commn. 31: 379–383.
- Buckland, S.T.; K.L. Cattanach and Th. Gunnlaugsson (1992). "Fin whale abundance in the North Atlantic, estimated from Icelandic and Faroese NASS-87 and NASS-89 data". Rep. Int. Whal. Commn. 42: 645–651.
- Rørvik, C.J.; J. Jónsson, O.A. Mathisen, and Å. Jonsgård (1976). "Fin Whales, Balaenoptera physalus (L.), Off the West Coast of Iceland. Distribution, Segregation by Length and Exploitation". Rit Fiskideildar. 5: 1–30. ISSN 0484-9019.
- Buckland, S.T.; K.L. Cattanach and S. Lens (1992). "Fin whale abundance in the eastern North Atlantic, estimated from Spanish NASS-89 data". Rep. Int. Whal. Commn. 42: 457–460.
- Bérubé, M.; Aguilar, A., Dendanto, D., Larsen, F., Notarbartolo di Sciara, G., Sears, R., Sigurjónsson, J., Urbán-R, J. and Palsbøll, P.J. (1998). "Population genetic structure of North Atlantic, Mediterranean Sea and Sea of Cortez Fin Whales, Balaenoptera physalus (Linnaeus 1758): analysis of mitochondrial and nuclear foci". Molecular Ecology. 7 (5): 585–599. doi:10.1046/j.1365-294x.1998.00359.x. ISSN 1471-8278. PMID 9633102.
- Fin Whales in Maltese waters
- Fin whale spotted close to Malta
- Whales in Maltese waters, and we hardly know about them!
- Pantelleria: la balena del 2008 (video)
- Panigada S., Donovan G., Druon N.-J., Lauriano G., Pierantonio N., Pirotta E., Zanardelli M., Zerbini A., 2015, Satellite telemetry on Mediterranean fin whales to identify critical habitats and mitigate ship strikes, SC/66a/HIM/14, International Whaling Commission
- Sardegna, avvistate 5 balenottere al largo di Cala Gonone /Video
- Satellite telemetry applied to fin whale in the Mediterranean Sea
- Lampedusa project (5 March 2013)
- Marini L., Germana Villetti G., Consiglio C., WINTERING AREAS OF FIN WHALES (BALAENOPTERA PHYSALUS) IN THE MEDITERRANEAN SEA: A PRELIMINARY SURVEY, pp.126-128
- Update on the Cetacean Fauna of the Mediterranean Levantine Basin
- Blue Fin Whale - Lebanon
- Action Plan for the Conservation of Cetaceans in Libya
- The Status and Distribution of Cetaceans in Black Sea and Mediterranean Sea
- Notarbartolo-Di-Sciara G., Zanardelli M., Jahoda M., Panigada S., Airoldi S. (2003). "The fin whale Balaenoptera physalus (L. 1758) in the Mediterranean Sea". Mammal Rev. 33 (2): 105–150.
- Fifth stranding record of the Fin Whale in Turkey
- Moore M., Lisa Steiner L., Jann B. (2003). "Cetacean surveys in the Cape Verde Islands and the use of cookiecutter shark bite lesions as a population marker for fin whales" (pdf). Aquatic Mammals. 29 (3): 383–389. doi:10.1578/AM.29.3.2003.383. Retrieved 2016-03-28.
- Ohsumi, S.; S. Wada (1974). "Status of whale stocks in the North Pacific, 1972". Rep. Int. Whal. Commn. 24: 114–126.
- Chapman, D.G. (1976). "Estimates of stocks (original, current, MSY level and MSY)(in thousands) as revised at Scientific Committee meeting 1975". Rep. Int. Whal. Commn. 26: 44–47.
- Barlow, J. (2003). "Preliminary estimates of the Abundance of Cetaceans along the U.S. West Coast: 1991–2001". Administrative report LJ-03-03, available from Southwest Fisheries Science Center, 8604 La Jolla Shores Dr., La Jolla CA 92037.
- Caretta, J.V.; K.A. Forney; M.M. Muto; J. Barlow; J. Baker; B. Hanson & M.S. Lowry (2006). "U.S. Pacific Marine Mammal Stock Assessments: 2005" (PDF). U.S. Department of Commerce Technical Memorandum, NOAA-TM-NMFS-SWFSC-388.
- Williams, R.; Thomas, L. (2007). "Distribution and abundance of marine mammals in the coastal waters of BC, Canada" (PDF). Journal of Cetacean Research and Management. 9: 15–28.
- Baretta, L.; G.L. Hunt Jr. (1994). "Changes in the numbers of cetaceans near the Pribilof Islands, Bering Sea, between 1975–78 and 1987–89" (PDF). Arctic. 47 (4): 321–326. doi:10.14430/arctic1304.
- Mizroch, S.A.; D.W. Rice, and J.M. Breiwick (1984). "The fin whale, Balaenoptera physalus". Mar Fish. Review. 46: 20–24.
- "Fin Whale Sighting Off the Coast of Vancouver Island". YouTube.
- Kotoe S. (2013). "釧路のすんごい思い出 その１". さかまた組 [kobemap.com/sakamata/]. Retrieved 13 May 2014.
- Yamada T., ed. (2009). "新潟県佐渡郡沢崎鼻沖種不明ナガスクジラ属クジラ目視". National Museum of Nature and Science. p. 海棲哺乳類情報データベース. Retrieved 13 January 2015.
- Mizroch A.S., Rice W.D., Zwiefelhofer D., Waite J., Perryman L.W. (2009). "Distribution and movements of fin whales in the North Pacific Ocean". p. The Wiley Online Library. Retrieved 24 December 2014.
- "第 2 章 こうちの生きもの Faunas of Kouchi Prefecture" (PDF). 生物多様性×こうち戦略. Retrieved 9 January 2015.
- "Maritime Information and Communication System – 福岡海上保安部 – 海洋生物目撃情報". Japanese Coast Guard. Retrieved 11 January 2015.
- Tsuji K., Kagami R., Shakata K., Kato H. (2013). "日本沿岸域における超高速船航路上の鯨類出現状況分析" (PDF). 第129回講演会（2013年11月8日,9日） 日本航海学会講演予稿集 1巻2号 2013年10月3日. Tokyo University of Marine Science and Technology, Nippon Kaiji Kyokai, Shinkawa Electric Co., Ltd. Retrieved 13 January 2015.
- Dolphin and Whale Save Project, 八重山周辺海域における鯨類ストライディングデータ（通過目撃等含む）
- Chang K., Zhang C., Park C., Kang D., Ju S., Lee S., Wimbush M., eds. (2015). "Oceanography of the East Sea (Japan Sea)". Springer International Publishing. p. 380. Retrieved 2015-09-08.
- Peilie W. (1978). "Studies on the baleen whales in the Yellow Sea". Acta Zoologica Sinica, 1978-03. Marine Fisheries Research Institute, Liaoning Province Fujian Natural History Museum. p. CNKI – The China National Knowledge Infrastructure. Retrieved 2015-09-07.
- Финвал (сельдяной кит) Balaenoptera physalus (Linnaeus, 1758)
- Finwhale in the Fiji Islands (Balaenoptera physalus)
- Travis Horton. "Humpback Whale Migration - Rarotonga, 2014".
- Fin whale - OceanSounds e.V.
- Toro F., Vilina A.Y., Capella J.J., Gibbons J. (2016). "Novel Coastal Feeding Area for Eastern South Pacific Fin Whales (Balaenoptera physalus) in Mid-Latitude Humboldt Current Waters off Chile" (pdf). Aquatic Mammals. 42 (1): 47–55. doi:10.1578/AM.42.1.2016.47. Retrieved 2016-03-31.
- Bicentinario Chile
- Pacheco1 S.A., Villegas K.V., Riascos M.J., Waerebeek V.K. (2015). "Presence of fin whales (Balaenoptera physalus) in Mejillones Bay, a major seaport area in northern Chile" (pdf). Revista de Biología Marina y Oceanografía Vol. 50, Nº2: DOI 10.4067/S0718-19572015000300017: 383–389. Retrieved 2016-03-31.
- Pacheco1 S.A., Villegas K.V., Riascos M.J., Waerebeek V.K. (2015). "Presence of fin whales (Balaenoptera physalus) in Mejillones Bay, a major seaport area in northern Chile" (pdf). Revista de Biología Marina y Oceanografía Vol. 50, Nº2: DOI 10.4067/S0718-19572015000300017: 383–389. Retrieved 2016-03-31.
- Acevedo J., O’Grady M., Wallis B. (2012). "Sighting of the fin whale in the Eastern Subtropical South Pacific: Potential breeding ground?" (pdf). Revista de Biología Marina y Oceanografía Vol. 47, Nº3. University of Valparaíso: 559–563. Retrieved 2016-03-31.
- IWC (1979). "Report of the sub-committee on protected species. Annex G, Appendix I". Rep. Int. Whal. Commn. 29: 84–86.
- "Orcas attack, kill large fin whale off La Paz (rare footage) – Pete Thomas Outdoors".
- Jefferson, T. A.,; Stacey, P. J.; Baird, R. W. (1991). "A review of killer whale interactions with other marine mammals: predation to co-existence" (PDF). Mammal Reviews. 21 (4): 151–180. doi:10.1111/j.1365-2907.1991.tb00291.x.
- Ford, John K. B.; Reeves, Randall R. (2008). "Fight or flight: Antipredator strategies of baleen whales". Mammal Review. 38 (1): 50–86. doi:10.1111/j.1365-2907.2008.00118.x.
- Nemoto, T.; A. Kawamura (1977). "Characteristics of food habits and distribution of baleen whales with special reference to the abundance of North Pacific sei and Bryde's whales". Rep. Int. Whal. Commn. Spec. Iss. 1: 80–87.
- Mizroch, S. A., Rice, D. W., Zwiefelhofer, D., Waite, J., and Perryman, W. L. (2009). "Distribution and movements of fin whales in the North Pacific Ocean". Mammal Rev. (39) 193–227.
- Flinn, R.D.; Trites, A.W.; Gregr, E. J.; Perry, R. I. (2002). "Diets of fin, sei, and sperm whales in British Columbia: an analysis of commercial whaling records, 1963–1967". Mar Mam. Sci. 18 (3): 663–679. doi:10.1111/j.1748-7692.2002.tb01065.x.
- Rice, D.W. (1977). "Synopsis of biological data on the sei whale and Bryde's whale in the eastern North Pacific". Rep. Int. Whal. Commn. Spec. Iss. 1: 92–97.
- Sigurjónsson, J.; Víkingsson, G. A. (1997). "Seasonal abundance of and estimated food consumption by cetaceans in Icelandic and adjacent waters". J. Northwest Atl. Fish. Sci. 22: 271–287. doi:10.2960/j.v22.a20.
- Canese, S.; Cardinali, A.; Fortuna, C. M.; Giusti, M.; Lauriano, G.; et al. (2006). "The first identified winter feeding ground of fin whales (Balaenoptera physalus) in the Mediterranean Sea". J. Mar Biol. Assoc. U.K. 86 (4): 903–907. doi:10.1017/s0025315406013853.
- Reeves, R.; G. Silber and M. Payne (July 1998). Draft Recovery Plan for the Fin Whale Balaenoptera physalus and Sei Whale Balaenoptera borealis (PDF). Silver Spring, Maryland: National Marine Fisheries Service.
- Reynolds, John Elliott, and Sentiel A. Rommel. (1999). Biology of Marine Mammals. Washington: Smithsonian Institution Press.
- S.L. Perry; D.P. DeMaster, and G.K. Silber (1999). "Special Issue: The Great Whales: History and Status of Six Species Listed as Endangered Under the U.S. Endangered Species Act of 1973". Marine Fisheries Review. 61 (1): 52–58.
- Lin, Brian (7 June 2007). "Whale Has Super-sized Big Gulp". University of British Columbia. Retrieved 8 June 2007.
- Çíçek, Erdoğan; Öktener, Ahmet; Çapar, Osman Bahadır (2007). "First Report of Pennella balaenopterae Koren and Danielssen, 1877 (Copepoda: Pennelidae) from Turkey" (PDF). Türkiye Parazitoloji Dergisi (Turkish Journal of Parasitology). 31 (3): 239–241. PMID 17918069.
- Rajaguru, Arjuna; Shantha, Gopalsamy (1992). "Association between the sessile barnacle Xenobalanus globiclpitis (Coronulidae) and the bottlenose dolphin Tursiops truncatus (Delphinidae) from the Bay of Bengal, India, with a summary of previous records from cetaceans" (PDF). Fishery Bulletin. 90: 197–202.
- Jauniaux, T.; Charlier, G.; Desmecht, M.; Coignoui, F. (1998). "Lesions of morbillivirus infection in a fin whale (Balaenoptera physalus) stranded along the Belgian coast". Veterinary Record. 143 (15): 423–424. doi:10.1136/vr.143.15.423. PMID 9807793.
- Mazzariol, Sandro; Marcer, Federica; Mignone, Walter; Serracca, Laura; Goria, Mariella; Marsili, Letizia; Giovanni, Giovanni; Guardo, Di; Casalone, Cristina; et al. (2012). "Dolphin Morbillivirus and Toxoplasma gondii coinfection in a Mediterranean fin whale (Balaenoptera physalus)". BMC Veterinary Research. 8 (1): 20. doi:10.1186/1746-6148-8-20.
- "American Cetacean Society Fact Sheet: Fin Whale, Balaenoptera physalus". American Cetacean Society. Retrieved 12 March 2012.
- IWC (1995). "Report of the scientific committee". Rep. Int. Whal. Commn. 45: 53–221.
- Barlow, J., K. A. Forney, P.S. Hill, R.L. Brownell Jr., J.V. Caretta, D.P. DeMaster, F. Julian, M.S. Lowry, T. Ragen, and R.R. Reeves (1997). "U.S. Pacific Marine Mammal Stock Assessments: 1996" (PDF). NOAA Technical Memo NMFD-SWFSC-248.
- International Whaling Statistics.
- Ishikawa H., Watanabe T. (2014). "A catalogue of whales and dolphins recorded in Yamaguchi Prefecture, Japan" (PDF). 下関鯨類研究室報告 No.2 (2014). Whale Laboratory of Shimonoseki. Retrieved 9 January 2015.
- Miyazaki N., Nakayama K. (1989). "Records of Cetaceans in the Waters of the Amami Island" (PDF). 国立科学博物館専報 22, 235–249, 1989. National Museum of Nature and Science, Museum of History and Folklore in Kasari. p. CiNii. Retrieved 2015-01-16.
- "海域自然環境保全基礎調査 – 海棲動物調査報告書, (2)- 19. シャチ Orcinus orca (Limaeus,1758)マイルカ科" (PDF). 自然環境保全基礎調査. Nature Conservation Bureau of Ministry of the Environment (Japan): 54. 1998. Retrieved 2015-01-16.
- Clapham, P. J.; Baker, C. Scott (2008). "Reported vs. Actual Catches by the U.S.S.R. in the Southern Hemisphere, 1948–73. Appendix II in Berzin, A. A.; trans. by Y. V. Ivashchenko. "The Truth About Soviet Whaling"". Marine Fisheries Review. 70 (2): 4–59.
- Clapham, P.J.; Brownell, R. L.; Jr (2008). "Soviet catches of large whales in the North Pacific, 1961–79. Appendix III in Berzin, A. A.; trans. by Y. V. Ivashchenko "The Truth About Soviet Whaling"". Marine Fisheries Review. 70 (2): 4–59.
- Yablokov, A.V. (1994). "Validity of whaling data". Nature. 367 (6459): 108. Bibcode:1994Natur.367..108Y. doi:10.1038/367108a0.
- "UNEP-WCMC Species Database: CITES-Listed Species". UNEP-WCMC. 23 October 2006. Retrieved 23 October 2006.
- "Species Profile for Finback whale". U.S. Fish & Wildlife Service. Retrieved 23 October 2006.
- "Iceland to Resume Whale Hunting, Defying Global Ban". Bloomberg.com. 18 October 2006. Retrieved 23 October 2006.
- "Catches under Objection". International Whaling Commission. Retrieved 6 February 2012.
- Revkin, Andrew C. (13 September 2014). "Should Fin Whales Be a Source of Wonder or Meat?". New York Times. Retrieved 14 September 2014.
- "U.S. Protests Japan's Announced Return to Whaling in Antarctic". Bureau of International Information Programs, U.S. Department of State. 20 November 2006. Retrieved 27 November 2006.
- "Catches under Permit". International Whaling Commission. Archived from the original on 18 June 2012. Retrieved 6 February 2012.
- Laist, D.W.; Knowlton, A.R., Mead, J.G., Collet A.S., and Podesta, M.; Mead, James G.; Collet, Anne S.; Podesta, Michela (2001). "Collisions between ships and whales" (PDF). Marine Mammal Science. 17 (1): 35–75. doi:10.1111/j.1748-7692.2001.tb00980.x.
- "Whale Found Dead on Bow of Ship Examined in New Jersey". Associated Press. Retrieved 17 April 2014.
- "The Fin Whale Passage – Natural History Museum of Los Angeles".
- Science North – Fourth Floor exhibits
- "Archived copy". Archived from the original on 21 January 2014. Retrieved 17 January 2014.
- "The mysterious death of young Leonora".
- "Permanent exhibitions – Hungarian Natural History Museum – Fin whale skeleton".
- "University Museum of Zoology, Cambridge – The Finback Whale".
- "Maritime". Otago Museum. Retrieved 13 May 2013.
- Whales Online – Fin whale
- "Irish Whale and Dolphin Group – Fin Whale Species Profile".
- "Appendix I and Appendix II Archived 11 June 2011 at the Wayback Machine." of the Convention on the Conservation of Migratory Species of Wild Animals (CMS). As amended by the Conference of the Parties in 1985, 1988, 1991, 1994, 1997, 1999, 2002, 2005 and 2008. Effective: 5 March 2009.
- "Accobams News".
- Peter Saundry. 2011. Fin whale. Encyclopedia of Earth. National Council for Science and the Environment. Washington DC. C. Michael Hogan Ed. Content partner: Encyclopedia of Life
- National Audubon Society Guide to Marine Mammals of the World, Reeves, Stewart, Clapham and Powell, ISBN 0-375-41141-0
- Whales & Dolphins Guide to the Biology and Behaviour of Cetaceans, Maurizio Wurtz and Nadia Repetto. ISBN 1-84037-043-2
- Encyclopedia of Marine Mammals, editors Perrin, Wursig and Thewissen, ISBN 0-12-551340-2
|Wikispecies has information related to: Balaenoptera physalus|
|Wikimedia Commons has media related to Balaenoptera physalus.|
- US National Marine Fisheries Service fin whale web page
- ARKive – images and videos of the fin whale (Balaenoptera physalus)
- Finback whale sounds
- IUCN Red List entry
- Photograph of a fin whale underwater
- Photographs of a fin whale breaching
- World Wide Fund for Nature (WWF) – species profile for the fin whale
- Voices in the Sea – Sounds of the Fin Whale