Baleen whales (systematic name Mysticeti), known earlier as whalebone whales, form a parvorder of the infraorder Cetacea (whales, dolphins and porpoises). They are a widely distributed and diverse parvorder of carnivorous marine mammals. Mysticeti comprise the families Balaenidae (right and bowhead whales), Balaenopteridae (rorquals), Cetotheriidae (the pygmy right whale), and Eschrichtiidae (the gray whale). There are currently 15 species of baleen whales. While cetaceans were historically thought to have descended from mesonychids, (which would place them outside the order Artiodactyla), molecular evidence supports them as a clade of even-toed ungulates (Artiodactyla). Baleen whales split from toothed whales (Odontoceti) around 34 million years ago.
Temporal range: late Eocene–Present
|Humpback whale breaching|
Baleen whales range in size from the 6 m (20 ft) and 3,000 kg (6,600 lb) pygmy right whale to the 31 m (102 ft) and 190 t (210 short tons) blue whale, the largest known animal to have ever existed. They are sexually dimorphic. Baleen whales can have streamlined or large bodies, depending on the feeding behavior, and two limbs that are modified into flippers. Though not as flexible and agile as seals, baleen whales can swim very fast, with the fastest able to travel at 37 kilometers per hour (23 mph). Baleen whales use their baleen plates to filter out food from the water by either lunge-feeding or skim-feeding. Baleen whales have fused neck vertebrae, and are unable to turn their head at all. Baleen whales have two blowholes. Some species are well adapted for diving to great depths. They have a layer of fat, or blubber, under the skin to keep warm in the cold water.
Although baleen whales are widespread, most species prefer the colder waters of the Arctic and Antarctic. Gray whales are specialized for feeding on bottom-dwelling crustaceans. Rorquals are specialized at lunge-feeding, and have a streamlined body to reduce drag while accelerating. Right whales skim-feed, meaning they use their enlarged head to effectively take in a large amount of water and sieve the slow-moving prey. Males typically mate with more than one female (polygyny), although the degree of polygyny varies with the species. Male strategies for reproductive success vary between performing ritual displays (whale song) or lek mating. Calves are typically born in the winter and spring months and females bear all the responsibility for raising them. Mothers fast for a relatively long period of time over the period of migration, which varies between species. Baleen whales produce a number of vocalizations, notably the songs of the humpback whale.
The meat, blubber, baleen, and oil of baleen whales have traditionally been used by the indigenous peoples of the Arctic. Once relentlessly hunted by commercial industries for these products, cetaceans are now protected by international law. However, the North Atlantic right whale is ranked endangered by the International Union for Conservation of Nature. Besides hunting, baleen whales also face threats from marine pollution and ocean acidification. It has been speculated that man-made sonar results in strandings. They have rarely been kept in captivity, and this has only been attempted with juveniles or members of one of the smallest species.
- 1 Taxonomy
- 2 Anatomy
- 3 Behavior
- 4 Relationship with humans
- 5 References
- 6 External links
Baleen whales are cetaceans classified under the parvorder Mysticeti, and consist of four extant families: Balaenidae (right whales), Balaenopteridae (rorquals), Cetotheriidae (pygmy right whale), and Eschrichtiidae (gray whale). Balaenids are distinguished by their enlarged head and thick blubber, while rorquals and gray whales generally have a flat head, long throat pleats, and are more streamlined than Balaenids. Rorquals also tend to be longer than the latter. Cetaceans (whales, dolphins, and porpoises) and artiodactyls are now classified under the order Cetartiodactyla, often still referred to as Artiodactyla (given that the cetaceans are deeply nested with the artiodactyls). The closest living relatives to baleen whales are toothed whales both from the infraorder Cetacea.
|Cladogram showing phylogenic relations between mysticete species according to Hassanin and Ropiquet, et al., Sasaki and Nikaido, et al., and Rosenbaum and Brownell, Jr., et al.|
Balaenidae consists of two genera: Eubalaena (right whales) and Balaena (the bowhead whale, B. mysticetus). Balaenidae was thought to have consisted of only one genus until studies done through the early 2000s reported that bowhead whales and right whales are morphologically (different skull shape) and phylogenically different. According to a study done by H. C. Rosenbaum (of the American Museum of Natural History) and colleagues, the North Pacific (E. japonica) and Southern right (E. australis) whales are more closely related to each other than to the North Atlantic right whale (E. glacialis).
Cetotheriidae consists of only one living member: the pygmy right whale (Caperea marginata). The first descriptions date back to the 1840s of bones and baleen plates resembling a smaller version of the right whale, and was named Balaena marginata. In 1864, it was moved into the genus Caperea after a skull of another specimen was discovered. Six years later, the pygmy right whale was classified under the family Neobalaenidae. Despite its name, the pygmy right whale is more genetically similar to rorquals and gray whales than to right whales. A study published in 2012, based on bone structure, moved the pygmy right whale from the family Neobalaenidae to the family Cetotheriidae, making it a living fossil; Neobalaenidae was elevated down to subfamily level as Neobalaeninae.
Rorquals consist of two genera (Balaenoptera and Megaptera) and nine species: the fin whale (B. physalus), the Sei whale (B. borealis), Bryde's whale (B. brydei), Eden's whale (B. edeni), the blue whale (B. musculus), the common minke whale (B. acutorostrata), the Antarctic minke whale (B. bonaerensis), Omura's whale (B. omurai), and the humpback whale (M. novaeangliae). In a 2012 review of cetacean taxonomy, Alexandre Hassanin (of the Muséum National d'Histoire Naturelle) and colleagues suggested that, based on phylogenic criteria, there are four extant genera of rorquals. They recommend that the genus Balaenoptera be limited to the fin whale, have minke whales fall under the genus Pterobalaena, and have Rorqualus contain the Sei whale, Bryde's whale, Eden's whale, the blue whale, and Omura's whale.
Eschrichtiidae consists of only one living member: the gray whale (Eschrichtius robustus). The two populations, one in the Sea of Okhotsk and Sea of Japan and the other in the Mediterranean Sea and East Atlantic, are thought to be genetically and physiologically dissimilar. However, there is some discussion as to whether the gray whale should be classified into its own family, or as a rorqual.,
The taxonomic name "Mysticeti" (// apparently derives from a translation error in early copies of Aristotle's Historia Animalium (in Ancient Greek), in which "ὁ μῦς τὸ κῆτος" (ho mus to kētos, "the mouse, the whale so called") was mistakenly translated as "ὁ μυστικῆτος" (ο mustikētos, "the Mysticetus"), which D. W. Rice (of the Society for Marine Mammalogy) in his 1998 work assumed was an ironic reference to the animals' great size. An alternate name for the parvorder is "Mystacoceti" (from Greek μύσταξ "mustache" + κῆτος "whale"), which, although obviously more appropriate and occasionally used in the past, has been superseded by "Mysticeti" (junior synonym).
Mysticetes are also known as baleen whales because of the presence of baleen. These animals rely on their baleen plates to sieve plankton and other small organisms from the water. The term "baleen" (Middle English baleyn, ballayne, ballien, bellane, etc.) is an archaic word for "whale", derived from the Latin word balæna.
Differences between familiesEdit
Rorquals use throat pleats to expand their mouths, which allow them to feed more effectively. However, rorquals need to build up water pressure in order to expand their mouths, leading to a lunge-feeding behavior. Lunge-feeding is where a whale rams a bait ball (a swarm of small fish) at high speed. Rorquals generally have streamlined physiques to reduce drag in the water while doing this. Balaenids rely on their huge heads, as opposed to the rorquals' throat pleats, to feed effectively. This feeding behavior allows them to grow very big and bulky, without the necessity for a streamlined body. They have callosities, unlike other whales, with the exception of the bowhead whale. Rorquals have a higher proportion of muscle tissue and tend to be negatively buoyant, whereas right whales have a higher proportion of blubber and are positively buoyant. Gray whales are easily distinguished from other extant cetaceans by their sleet-gray color, dorsal ridges (knuckles on the back), and their gray-white scars left from parasites. As with the rorquals, their throat pleats increase the capacity of their throats, allowing them to filter larger volumes of water at once. Gray whales are bottom-feeders, meaning they sift through sand to get their food. They usually turn on their sides, scoop up sediment into their mouths and filter out benthic creatures like amphipods, which leave noticeable marks on their heads. The pygmy right whale is easily confused with minke whales because of their similar characteristics, such as their small size, dark gray tops, light gray bottoms, and light eye-patches.
- The "†" signs denote extinct families and genera.
- Parvorder Mysticeti: baleen whales
- Family †Aetiocetidae
- †Family Llanocetidae
- †Family Mammalodontidae
- †Family Mystacodontidae
- Clade Chaeomysticeti
- Superfamily Eomysticetoidea
- Clade Balaenomorpha
- Superfamily Balaenoidea
- Clade Thalassotherii
- Family †Aglaocetidae
- †Family Diorocetidae
- †Family Pelocetidae
- †Family Tranatocetidae
- Family Cetotheriidae
- Family Neobalaenidae
- Superfamily Balaenopteroidea
- Family Balaenopteridae: rorquals
- Family Eschrichtiidae
- incertae sedis
- Parvorder Mysticeti: baleen whales
Mysticeti split from Odontoceti (toothed whales) 26 to 17 million years ago during the Eocene. Their evolutionary link to archaic toothed cetaceans (Archaeoceti) remained unknown until the extinct Janjucetus hunderi was discovered in the early 1990s in Victoria, Australia. Like a modern baleen whale, Janjucetus had baleen in its jaw and had very little biosonar capabilities. However, its jaw also contained teeth, with incisors and canines built for stabbing and molars and premolars built for tearing. These early mysticetes were exceedingly small compared to modern baleen whales, with species like Mammalodon measuring no greater than 3 meters (10 ft). It is thought that their size increased with their dependence on baleen. However, the discovery of a skull of the toothed Llanocetus, the second-oldest mysticete, yielded a total length of 8 meters (26 ft), indicating filter feeding was not a driving feature in mysticete evolution. The discovery of Janjucetus and others like it suggests that baleen evolution went through several transitional phases. Species like Mammalodon colliveri had little to no baleen, while later species like Aetiocetus weltoni had both baleen and teeth, suggesting they had limited filter feeding capabilities; later genera like Cetotherium had no teeth in their mouth, meaning they were fully dependent on baleen and could only filter feed. However, the 2018 discovery of the toothless Maiabalaena indicates some lineages evolved toothlessness before baleen.
Mystacodon selenensis is the earliest mysticete, dating back to 37 to 33 million years ago (mya) in the Late Eocene, and, like other early toothed mysticetes, or "archaeomysticetes", M. selenensis had heterodont dentition used for suction feeding. Archaeomysticetes from the Oligocene are the Mammalodontidae (Mammalodon and Janjucetus) from Australia. They were small with shortened rostra, and a primitive dental formula (126.96.36.199). In baleen whales, it is thought that enlarged mouths adapted for suction feeding evolved before specializations for bulk filter feeding. In the toothed Oligocene mammalodontid Janjucetus, the symphysis is short and the mouth enlarged, the rostrum is wide, and the edges of the maxillae are thin, indicating an adaptation for suction feeding. The aetiocetid Chonecetus still had teeth, but the presence of a groove on the interior side of each mandible indicates the symphysis was elastic, which would have enabled rotation of each mandible, an initial adaptation for bulk feeding like in modern mysticetes.
The first toothless ancestors of Mysticetes appeared before the first radiation in the late Oligocene. Eomysticetus and others like it showed no evidence in the skull of echolocation abilities, suggesting they mainly relied on their eyesight for navigation. The eomysticetes had long, flat rostra that lacked teeth and had blowholes located halfway up the dorsal side of the snout. Though the palate is not well-preserved in these specimens, they are thought to have had baleen and been filter feeders. Miocene baleen whales were preyed upon by larger predators like killer sperm whales and Megalodon.
The lineages of rorquals and right whales split almost 20 mya. It is unknown where this occurred, but it is generally believed that they, like their descendants, followed plankton migrations. These primitive mysticetes had lost their heterodont dentition in favor of baleen, and are believed to have lived on a specialized benthic, plankton, or copepod diet like modern mysticetes. Mysticetes experienced their first radiation in the mid-Miocene. It is thought this radiation was caused by global climate change and major tectonic activity when Antarctica and Australia separated from each other, creating the Antarctic Circumpolar Current. Balaenopterids grew bigger during this time, with species like Balaenoptera sibbaldina perhaps rivaling the blue whale in terms of size, though many other studies disagree that any mysticetes grew that large in the miocene.
The increase in size is likely due to shifts in climate that have resulted in seasonally shifting accumulations of plankton in various parts of the world, necessitating more efficiency traveling over long distances between widely distributed prey sources which also resulted in a lower metabolic rate, and feeding on baitballs. A 2017 analysis of body size based on data from the fossil record and modern mysticetes indicates that the evolution of gigantism in baleen whales is a recent phenomenon, estimated to have occurred within the past 3.1 Ma. Before 4.5 million years ago, few mysticetes exceeded 10 meters (33 feet) in length; the two largest miocene species were less than 13 m in length. The initial evolution of baleen and filter feeding long preceded the evolution of gigantic body size, indicating the evolution of novel feeding mechanisms did not cause the evolution of gigantism. The creation of the Antarctic circumpolar current and its effects on global climate patterns is excluded as being causal for the same reason. Gigantism also was preceded by divergence of different mysticete lineages, meaning multiple lineages arrived at large size independently. It is possible the Plio-Pleistocene increase in seasonally intense upwellings causing high-prey-density zones led to gigantism.
When swimming, baleen whales rely on their flippers for locomotion in a wing-like manner similar to penguins and sea turtles. Flipper movement is continuous. While doing this, baleen whales use their tail fluke to propel themselves forward through vertical motion while using their flippers for steering, much like an otter. Some species leap out of the water, which may allow them to travel faster. Because of their great size, right whales are not flexible or agile like dolphins, and none can move their neck because of the fused cervical vertebrae; this sacrifices speed for stability in the water. The hind legs are enclosed inside the body, and are thought to be vestigial organs. However, a 2014 study suggests that the pelvic bone serves as support for whale genitalia.
Rorquals, needing to build speed to feed, have several adaptions for reducing drag, including a streamlined body; a small dorsal fin, relative to its size; and lack of external ears or long hair. The fin whale, the fastest among baleen whales, can travel at 37 kilometers per hour (23 mph). While feeding, the rorqual jaw expands to a volume that can be bigger than the whale itself; to do this, the mouth inflates. The inflation of the mouth causes the cavum ventrale, the throat pleats on the underside stretching to the navel, to expand, increasing the amount of water that the mouth can store. The mandible is connected to the skull by dense fibers and cartilage (fibrocartilage), allowing the jaw to swing open at almost a 90° angle. The mandibular symphysis is also fibrocartilaginous, allowing the jaw to bend which lets in more water. To prevent stretching the mouth too far, rorquals have a sensory organ located in the middle of the jaw to regulate these functions.
Baleen whales have two flippers on the front, near the head. Like all mammals, baleen whales breathe air and must surface periodically to do so. Their nostrils, or blowholes, are situated at the top of the cranium. Baleen whales have two blowholes, as opposed to toothed whales which have one. These paired blowholes are longitudinal slits that converge anteriorly and widen posteriorly, which causes a V-shaped blow. They are surrounded by a fleshy ridge that keeps water away while the whale breathes. The septum that separates the blowholes has two plugs attached to it, making the blowholes water-tight while the whale dives.
Like other mammals, the skin of baleen whales has an epidermis, a dermis, a hypodermis, and connective tissue. The epidermis, the pigmented layer, is 5 millimeters (0.2 in) thick, along with connective tissue. The epidermis itself is only 1 millimeter (0.04 in) thick. The dermis, the layer underneath the epidermis, is also thin. The hypodermis, containing blubber, is the thickest part of the skin and functions as a means to conserve heat. Right whales have the thickest hypodermis of any cetacean, averaging 51 centimeters (20 in), though, as in all whales, it is thinner around openings (such as the blowhole) and limbs. Blubber may also be used to store energy during times of fasting. The connective tissue between the hypodermis and muscles allows only limited movement to occur between them. Unlike in toothed whales, baleen whales have small hairs on the top of their head, stretching from the tip of the rostrum to the blowhole, and, in right whales, on the chin. Like other marine mammals, they lack sebaceous and sweat glands.
The baleen of baleen whales are keratinous plates. They are made of a calcified, hard α-keratin material, a fiber-reinforced structure made of intermediate filaments (proteins). The degree of calcification varies between species, with the sei whale having 14.5% hydroxyapatite, a mineral that coats teeth and bones, whereas minke whales have 1–4% hydroxyapatite. In most mammals, keratin structures, such as wool, air-dry, but aquatic whales rely on calcium salts to form on the plates to stiffen them. Baleen plates are attached to the upper jaw and are absent in the mid-jaw, forming two separate combs of baleen. The plates decrease in size as they go further back into the jaw; the largest ones are called the "main baleen plates" and the smallest ones are called the "accessory plates". Accessory plates taper off into small hairs.
Unlike other whales (and most other mammals), the females are larger than the males. Sexual dimorphism is usually reversed, with the males being larger, but the females of all baleen whales are usually five percent larger than males. Sexual dimorphism is also displayed through whale song, notably in humpback whales where the males of the species sing elaborate songs. Male right whales have bigger callosities than female right whales. The males are generally more scarred than females which is thought to be because of aggression during mating season.
The unique lungs of baleen whales are built to collapse under the pressure instead of resisting the pressure which would damage the lungs, enabling some, like the fin whale, to dive to a depth of −470 meters (−1,540 ft). The whale lungs are very efficient at extracting oxygen from the air, usually 80%, whereas humans only extract 20% of oxygen from inhaled air. Lung volume is relatively low compared to terrestrial mammals because of the inability of the respiratory tract to hold gas while diving. Doing so may cause serious complications such as embolism. Unlike other mammals, the lungs of baleen whales lack lobes and are more sacculated. Like in humans, the left lung is smaller than the right to make room for the heart. To conserve oxygen, blood is rerouted from pressure-tolerant-tissue to internal organs, and they have a high concentration of myoglobin which allows them to hold their breath longer.
The heart of baleen whales functions similarly to other mammals, with the major difference being the size. The heart can reach 454 kilograms (1,000 lb), but is still proportional to the whale's size. The muscular wall of the ventricle, which is responsible for pumping blood out of the heart, can be 7.6 to 12.7 centimeters (3 to 5 in) thick. The aorta, an artery, can be 1.9 centimeters (.75 in) thick. Their resting heart rate is 60 to 140 beats per minute (bpm), as opposed to the 60 to 100 bpm in humans. When diving, their heart rate will drop to 4 to 15 bpm to conserve oxygen. Like toothed whales, they have a dense network of blood vessels (rete mirabile) which prevents heat-loss. Like in most mammals, heat is lost in their extremities, so, in baleen whales, warm blood in the arteries is surrounded by veins to prevent heat loss during transport. As well as this, heat inevitably given off by the arteries warms blood in the surrounding veins as it travels back into the core. This is otherwise known as countercurrent exchange. To counteract overheating while in warmer waters, baleen whales reroute blood to the skin to accelerate heat-loss. They have the largest blood corpuscles (red and white blood cells) of any mammal, measuring 10 micrometers (4.1×10−4 in) in diameter, as opposed to human's 7.1-micrometer (2.8×10−4 in) blood corpuscles.
When sieved from the water, food is swallowed and travels through the esophagus where it enters a three-chambered-stomach. The first compartment is known as the fore-stomach; this is where food gets ground up into an acidic liquid, which is then squirted into the main stomach. Like in humans, the food is mixed with hydrochloric acid and protein-digesting enzymes. Then, the partly digested food is moved into the third stomach, where it meets fat-digesting enzymes, and is then mixed with an alkaline liquid to neutralize the acid from the fore-stomach to prevent damage to the intestinal tract. Their intestinal tract is highly adapted to absorb the most nutrients from food; the walls are folded and contain copious blood vessels, allowing for a greater surface area over which digested food and water can be absorbed. Baleen whales get the water they need from their food; however, the salt content of most of their prey (invertebrates) are similar to that of seawater, whereas the salt content of a whale's blood is considerably lower (three times lower) than that of seawater. The whale kidney is adapted to excreting excess salt; however, while producing urine more concentrated than seawater, it wastes a lot of water which must be replaced.
Baleen whales have a relatively small brain compared to their body mass. Like other mammals, their brain has a large, folded cerebrum, the part of the brain responsible for memory and processing sensory information. Their cerebrum only makes up about 68% of their brain's weight, as opposed to human's 83%. The cerebellum, the part of the brain responsible for balance and coordination, makes up 18% of their brain's weight, compared to 10% in humans, which is probably due to the great degree of control necessary for constantly swimming. Necropsies on the brains of gray whales revealed iron oxide particles, which may allow them to find magnetic north like a compass.
Unlike most animals, whales are conscious breathers. All mammals sleep, but whales cannot afford to become unconscious for long because they may drown. They are believed to exhibit unihemispheric slow-wave sleep, in which they sleep with half of the brain while the other half remains active. This behavior was only documented in toothed whales until footage of a humpback whale sleeping (vertically) was shot in 2014.
It is largely unknown how baleen whales produce sound because of the lack of a melon and vocal cords. In a 2007 study, it was discovered that the larynx had U-shaped folds which are thought to be similar to vocal cords. They are positioned parallel to air flow, as opposed to the perpendicular vocal cords of terrestrial mammals. These may control air flow and cause vibrations. The walls of the larynx are able to contract which may generate sound with support from the arytenoid cartilages. The muscles surrounding the larynx may expel air rapidly or maintain a constant volume while diving.
The eyes of baleen whales are relatively small for their size and are positioned near the end of the mouth. This is probably because they feed on slow or immobile prey, combined with the fact that most sunlight does not pass 9.1 meters (30 ft), and hence they do not need acute vision. A whale's eye is adapted for seeing both in the euphotic and aphotic zones by increasing or decreasing the pupil's size to prevent damage to the eye. As opposed to land mammals which have a flattened lens, whales have a spherical lens. The retina is surrounded by a reflective layer of cells (tapetum lucidum), which bounces light back at the retina, enhancing eyesight in dark areas. However, light is bent more near the surface of the eye when in air as opposed to water; consequently, they can see much better in the air than in the water. The eyeballs are protected by a thick outer layer to prevent abrasions, and an oily fluid (instead of tears) on the surface of the eye. Baleen whales appear to have limited color vision, as they lack S-cones.
The mysticete ear is adapted for hearing underwater, where it can hear sound frequencies as low as 7 Hz and as high as 22 kHz. It is largely unknown how sound is received by baleen whales. Unlike in toothed whales, sound does not pass through the lower jaw. The auditory meatus is blocked by connective tissue and an ear plug, which connects to the eardrum. The inner-ear bones are contained in the tympanic bulla, a bony capsule. However, this is attached to the skull, suggesting that vibrations passing through the bone is important. Sinuses may reflect vibrations towards the cochlea. It is known that when the fluid inside the cochlea is disturbed by vibrations, it triggers sensory hairs which send electrical current to the brain, where vibrations are processed into sound.
Baleen whales have a small, yet functional, vomeronasal organ. This allows baleen whales to detect chemicals and pheromones released by their prey. It is thought that 'tasting' the water is important for finding prey and tracking down other whales. They are believed to have an impaired sense of smell due to the lack of the olfactory bulb, but they do have an olfactory tract. Baleen whales have few if any taste buds, suggesting they have lost their sense of taste. They do retain salt-receptor taste-buds suggesting that they can taste saltiness.
Most species of baleen whale migrate long distances from high latitude waters during spring and summer months to more tropical waters during winter months. This migration cycle is repeated annually. The gray whale has the longest recorded migration of any mammal, with one traveling 23,000 kilometers (14,000 mi) from the Sea of Okhotsk to the Baja Peninsula.
It is thought that plankton blooms dictate where whales migrate. Many baleen whales feed on the massive plankton blooms that occur in the cold, nutrient rich waters of polar regions during the sunny spring and summer months. Baleen whales generally then migrate to calving grounds in tropical waters during the winter months when plankton populations are low. Migration is hypothesized to benefit calves in a number of ways. Newborns, born with underdeveloped blubber, would likely otherwise be killed by the cold polar temperatures. Migration to warmer waters may also reduce the risk of calves being predated on by killer whales.
Migratory movements may also reflect seasonally shifting patterns of productivity. California blue whales are hypothesized to migrate between dense patches of prey, moving from central California in the summer and fall, to the Gulf of California in the winter, to the central Baja California Pacific coast in spring.
All modern mysticetes are obligate filter feeders, using their baleen to strain small prey items (including small fish, krill, copepods, and zooplankton) from seawater. Despite their carnivorous diet, a 2015 study revealed they house gut flora similar to that of terrestrial herbivores. Different kinds of prey are found in different abundances depending on location, and each type of whale is adapted to a specialized way of foraging.
There are two types of feeding behaviors: skim-feeding and lunge-feeding, but some species do both depending on the type and amount of food. Lunge-feeders feed primarily on euphausiids (krill), though some smaller lunge feeders (e.g. minke whales) also prey on schools of fish. Skim-feeders, like bowhead whales, feed upon primarily smaller plankton such as copepods. They feed alone or in small groups. Baleen whales get the water they need from their food, and their kidneys excrete excess salt.
The lunge-feeders are the rorquals. To feed, lunge-feeders expand the volume of their jaw to a volume bigger than the original volume of the whale itself. To do this, the mouth inflates, which causes the throat pleats to expand, increasing the amount of water that the mouth can store. Just before they ram the baitball, the jaw swings open at almost a 90° angle and bends which lets in more water. To prevent stretching the mouth too far, rorquals have a sensory organ located in the middle of the jaw to regulate these functions. Then they must decelerate. This process takes a lot of mechanical work, and is only energy-effective when used against a large baitball. Lunge feeding is more energy intensive than skim-feeding due to the acceleration and deceleration required.
The skim-feeders are right whales, gray whales, pygmy right whales, and sei whales (which also lunge feed). To feed, skim-feeders swim with an open mouth, filling it with water and prey. Prey must occur in sufficient numbers to trigger the whale's interest, be within a certain size range so that the baleen plates can filter it, and be slow enough so that it cannot escape. The "skimming" may take place on the surface, underwater, or even at the ocean's bottom, indicated by mud occasionally observed on right whales' bodies. Gray whales feed primarily on the ocean's bottom, feeding on benthic creatures.
Foraging efficiency for both lunge feeding and continuous ram filter feeding is highly dependent upon prey density. The efficiency of a blue whale lunge is approximately 30 times higher at krill densities of 4.5 kg/m3 than at low krill densities of 0.15 kg/m3. Baleen whale have been observed seeking out highly specific areas within the local environment in order to forage at the highest density prey aggregations.
Predation and parasitismEdit
Baleen whales, primarily juveniles and calves, are preyed on by killer whales. It is thought that annual whale migration occurs to protect the calves from the killer whales. There have also been reports of a pod of killer whales attacking and killing an adult bowhead whale, by holding down its flippers, covering the blowhole, and ramming and biting until death. Generally, a mother and calf pair, when faced with the threat of a killer whale pod, will either fight or flee. Fleeing only occurs in species that can swim away quickly, the rorquals. Slower whales must fight the pod alone or with a small family group. There has been one report of a shark attacking and killing a whale calf. This occurred in 2014 during the sardine run when a shiver of dusky sharks attacked a humpback whale calf. Usually, the only shark that will attack a whale is the cookie cutter shark, which leaves a small, non-fatal bite mark.
Many parasites latch onto whales, notably whale lice and whale barnacles. Almost all species of whale lice are specialized towards a certain species of whale, and there can be more than one species per whale. Whale lice eat dead skin, resulting in minor wounds in the skin. Whale louse infestations are especially evident in right whales, where colonies propagate on their callosities. Though not a parasite, whale barnacles latch onto the skin of a whale during their larval stage. However, in doing so it does not harm nor benefit the whale, so their relationship is often labeled as an example of commensalism. Some baleen whales will deliberately rub themselves on substrate to dislodge parasites. Some species of barnacle, such as Conchoderma auritum and whale barnacles, attach to the baleen plates, though this seldom occurs. A species of copepod, Balaenophilus unisetus, inhabits baleen plates of whales in tropical waters. A species of Antarctic diatom, Cocconeis ceticola, forms a film on the skin, which takes a month to develop; this film causes minor damage to the skin. They are also plagued by internal parasites such as stomach worms, cestodes, nematodes, liver flukes, and acanthocephalans.
Reproduction and developmentEdit
Before reaching adulthood, baleen whales grow at an extraordinary rate. In the blue whale, the largest species, the fetus grows by some 100 kg (220 lb) per day just before delivery, and by 80 kg (180 lb) per day during suckling. Before weaning, the calf increases its body weight by 17 t (17 long tons; 19 short tons) and grows from 7 to 8 m (23 to 26 ft) at birth to 13 to 16 m (43 to 52 ft) long. When it reaches sexual maturity after 5–10 years, it will be 20 to 24 m (66 to 79 ft) long and possibly live as long as 80–90 years. Calves are born precocial, needing to be able to swim to the surface at the moment of their birth.
Most rorquals mate in warm waters in winter to give birth almost a year later. A 7-to-11 month lactation period is normally followed by a year of rest before mating starts again. Adults normally start reproducing when 5–10 years old and reach their full length after 20–30 years. In the smallest rorqual, the minke whale, 3 m (10 ft) calves are born after a 10-month pregnancy and weaning lasts until it has reached about 5 to 5.5 m (16 to 18 ft) after 6–7 months. Unusual for a baleen whale, female minkes (and humpbacks) can become pregnant immediately after giving birth; in most species, there is a two-to-three-year calving period. In right whales, the calving interval is usually three years. They grow very rapidly during their first year, after which they hardly increase in size for several years. They reach sexual maturity when 13 to 14 m (43 to 46 ft) long. Baleen whales are K-strategists, meaning they raise one calf at a time, have a long life-expectancy, and a low infant mortality rate. Some 19th century harpoons found in harvested bowheads indicate this species can live more than 100 years. Baleen whales are promiscuous, with none showing pair bonds. They are polygynous, in that a male may mate with more than one female. The scars on male whales suggest they fight for the right to mate with females during breeding season, somewhat similar to lek mating.
Baleen whales have fibroelastic (connective tissue) penises, similar to those of artiodactyls. The tip of the penis, which tapers toward the end, is called the pars intrapraeputialis or terminal cone. The blue whale has the largest penis of any organism on the planet, typically measuring 2.4–3.0 metres (8–10 ft). Accurate measurements of the blue whale are difficult to take because the whale's erect length can only be observed during mating. The penis on a right whale can be up to 2.7 m (8.9 ft) – the testes, at up to 2 m (6.6 ft) in length, 78 cm (2.56 ft) in diameter, and weighing up to 238 kg (525 lb), are also the largest of any animal on Earth.
All baleen whales use sound for communication and are known to "sing", especially during the breeding season. Blue whales produce the loudest sustained sounds of any animals: their low-frequency (about 20 Hz) moans can last for half a minute, reach almost 190 decibels, and be heard hundreds of kilometers away. Adult male humpbacks produce the longest and most complex songs; sequences of moans, groans, roars, sighs, and chirps sometimes lasting more than ten minutes are repeated for hours. Typically, all humpback males in a population sing the same song over a breeding season, but the songs change slightly between seasons, and males in one population have been observed adapting the song from males of a neighboring population over a few breeding seasons.
Unlike their toothed whale counterparts, baleen whales are hard to study because of their immense size. Intelligence tests such as the mirror test cannot be done because their bulk and lack of body language makes a reaction impossible to be definitive. However, studies on the brains of humpback whales revealed spindle cells, which, in humans, control theory of mind. Because of this, it is thought that baleen whales, or at least humpback whales, have consciousness.
Relationship with humansEdit
History of whalingEdit
Whaling by humans has existed since the Stone Age. Ancient whalers used harpoons to spear the bigger animals from boats out at sea. People from Norway started hunting whales around 4,000 years ago, and people from Japan began hunting whales in the Pacific at least as early as that. Whales are typically hunted for their meat and blubber by aboriginal groups; they used baleen for baskets or roofing, and made tools and masks out of bones. The Inuit hunted whales in the Arctic Ocean. The Basques started whaling as early as the 11th century, sailing as far as Newfoundland in the 16th century in search of right whales. 18th and 19th century whalers hunted down whales mainly for their oil, which was used as lamp fuel and a lubricant, and baleen (or whalebone), which was used for items such as corsets and skirt hoops. The most successful whaling nations at this time were the Netherlands, Japan, and the United States.
Commercial whaling was historically important as an industry well throughout the 19th and 20th centuries. Whaling was at that time a sizable European industry with ships from Britain, France, Spain, Denmark, the Netherlands, and Germany, sometimes collaborating to hunt whales in the Arctic. By the early 1790s, whalers, namely the British (Australian) and Americans, started to focus efforts in the South Pacific; in the mid 1900s, over 50,000 humpback whale were taken from the South Pacific. At its height in the 1880s, U.S. profits turned to USD10,000,000, equivalent to US$225,000,000 today. Commonly exploited species included arctic whales such as the gray whale, right whale, and bowhead whale because they were close to the main whaling ports, like New Bedford. After those stocks were depleted, rorquals in the South Pacific were targeted by nearly all whaling organizations; however, they often out-swam whaling vessels. Whaling rorquals was not effective until the harpoon cannon was invented in the late 1860s. Whaling basically stopped when stocks of all species were depleted to a point that they could not be harvested on a commercial scale. Whaling was controlled in 1982 when the International Whaling Commission (IWC) placed a moratorium setting catch limits to protect species from dying out from over-exploitation, and eventually banned it:
Notwithstanding the other provisions of paragraph 10, catch limits for the killing for commercial purposes of whales from all stocks for the 1986 coastal and the 1985/86 pelagic seasons and thereafter shall be zero. This provision will be kept under review, based upon the best scientific advice, and by 1990 at the latest the Commission will undertake a comprehensive assessment of the effects of this decision on whale stocks and consider modification of this provision and the establishment of other catch limits.
–IWC Commission Schedule, paragraph 10(e)
Conservation and management issuesEdit
As of 2013, the International Union for Conservation of Nature (IUCN) recognizes 15 mysticete species. One species—the North Atlantic right whale—is endangered with only around 400(±50) individuals left, and four more are also classified as endangered (North Pacific right whale, the blue whale, the fin whale, and the Sei whale), and another 5 ranked as Data deficient (Bryde's whale, Eden's whale, Omura's whale, Southern minke whale, and pygmy right whale). Species that live in polar habitats are vulnerable to the effects of ongoing climate change, particularly declines in sea ice, as well as ocean acidification.
The whale-watching industry and anti-whaling advocates argue that whaling catches "friendly" whales that are curious about boats, as these whales are the easiest to catch. This analysis claims that once the economic benefits of hotels, restaurants and other tourist amenities are considered, hunting whales is a net economic loss. This argument is particularly contentious in Iceland, as it has among the most-developed whale-watching operations in the world and the hunting of minke whales resumed in August 2003. Brazil, Argentina and South Africa argue that whale watching is a growing billion-dollar industry that provides more revenue than commercial whaling would provide. Peru, Uruguay, Australia, and New Zealand also support proposals to permanently forbid whaling south of the Equator, as Solor (an island of Indonesia) is the only place of the Southern Hemisphere that takes whales. Anti-whaling groups, such as the International Fund for Animal Welfare (IFAW), claim that countries which support a pro-whaling stance are damaging their economies by driving away anti-whaling tourists.
Commercial whaling was historically important for the world economy. All species were exploited, and as one type's stock depleted, another type was targeted. The scale of whale harvesting decreased substantially through the 1960s as all whale stocks had been depleted, and practically stopped in 1988 after the International Whaling Commission placed a moratorium which banned whaling for commercial use.:327–333 Several species that were commercially exploited have rebounded in numbers; for example, gray whales may be as numerous as they were prior to whaling, making it the first marine mammal to be taken off the endangered species list. The Southern right whale was hunted to near extinction in the mid-to-late 20th century, with only a small (unknown) population around Antarctica. Because of international protection, the Southern right whale's population has been growing 7% annually since 1970. Conversely, the eastern stock of North Atlantic right whale was extirpated from much of its former range, which stretched from the coast of North Africa to the North Sea and Iceland; it is thought that the entire stock consists of only ten individuals, making the eastern stock functionally extinct.
Baleen whales continue to be harvested. Only three nations take whales: Iceland, Norway, and Japan. All these nations are part of the IWC, with Norway and Iceland rejecting the moratorium and continuing commercial whaling. Japan, being part of the IWC, whales under the Scientific Permit stated in Article VIII in the Convention for the Regulation of Whaling, which allows the taking of whales for scientific research. Japan has had two main research programs: the Joint Aquatic Resources Permit Application (JARPA) and the Japanese Research Program in the North (JARPN). JARPN is focused in the North Pacific and JARPA around the Antarctic. JARPA mainly caught Antarctic minke whales, catching nearly 7,000; to a far lesser extent, they also caught fin whales. Animal-rights activist groups, such as the Greenpeace, object to Japan's scientific whaling, with some calling it a substitute for commercial whaling. In 2014, the International Court of Justice (the UN judicial branch) banned the taking of whales for any purpose in the Southern Ocean Whale Sanctuary; however, Japan refuses to stop whaling and has only promised to cut their annual catches by a third (around 300 whales per year).
Baleen whales can also be affected by humans in more indirect ways. For species like the North Atlantic right whale, which migrates through some of the world's busiest shipping lanes, the biggest threat is from being struck by ships. The Lloyd's mirror effect results in low frequency propeller sounds not being discernible near the surface, where most accidents occur. Combined with spreading and acoustic shadowing effects, the result is that the whale is unable to hear an approaching vessel before it has been run over or entrapped by the hydrodynamic forces of the vessel's passage. A 2014 study noted that a lower vessel speed correlated with lower collision rates. The ever-increasing amount of ocean noise, including sonar, drowns out the vocalizations produced by whales, notably in the blue whale which produces the loudest vocalization, which makes it harder for them to communicate. Blue whales stop producing foraging D calls once a mid-frequency sonar is activated, even though the sonar frequency range (1–8 kHz) far exceeds their sound production range (25–100 Hz). Poisoning from toxic substances such as polychlorinated biphenyl (PCB) is generally low because of their low trophic level. Some baleen whales can become victims of bycatch, which is especially serious for North Atlantic right whales considering its small number. Right whales feed with a wide-open mouth, risking entanglement in any rope or net fixed in the water column. Rope wraps around their upper jaw, flippers and tail. Some are able to escape, but others remain entangled. If observers notice, they can be successfully disentangled, but others die over a period of months. Other whales, such as humpback whales, can also be entangled.
Baleen whales have rarely been kept in captivity. Their large size and appetite make them expensive creatures to maintain. Pools of proper size would also be very expensive to build. For example, a single gray whale calf would need to eat 215 kilograms (475 lb) of fish per day, and the pool would have to accommodate the 4-meter (13 ft) calf, along with ample room to swim. Only gray whales have survived being kept in captivity for over a year. The first gray whale, which was captured in Scammon's Lagoon, Baja California Sur, in 1965, was named Gigi and died two months later from an infection. The second gray whale, which was captured in 1971 from the same lagoon, was named Gigi II and was released a year later after becoming too big. The last gray whale, J.J., beached itself in Marina del Rey, California, where it was rushed to SeaWorld San Diego and, after 14 months, was released because it got too big to take care of. Reaching 8,700 kilograms (19,200 lb) and 9.4 meters (31 ft), J.J. was the largest creature to be kept in captivity. The Mito Aquarium in Numazu, Shizuoka, Japan, housed three minke whales in the nearby bay enclosed by nets. One survived for three months, another (a calf) survived for two weeks, and another was kept for over a month before breaking through the nets.
- Paul, Gregory S. (25 October 2016). The Princeton Field Guide to Dinosaurs (Second ed.). Princeton University Press. p. 19. ISBN 978-1-4008-8314-1.
- Bortolotti, Dan (14 October 2008). Wild Blue: A Natural History of the World's Largest Animal. St. Martin's Press. ISBN 978-1-4299-8777-6.
- Woodward, Becky L.; Winn, Jeremy P.; Fish, Frank E. (2006). "Morphological Specializations of Baleen Whales Associated With Hydrodynamic Performance and Ecological Niche" (PDF). Journal of Morphology. 267 (11): 1284–1294. doi:10.1002/jmor.10474. PMID 17051544. Archived from the original (PDF) on 2016-03-05.
- Crane, J.; Scott, R. (2002). "Eubalaena glacialis: North Atlantic right whale: Information". Animal Diversity Web. University of Michigan Museum of Zoology. Retrieved 25 January 2016.
- Minasian, Stanley M.; Balcomb, Kenneth C.; Foster, Larry, eds. (1984). The World's Whales: The Complete Illustrated Guide. New York: The Smithsonian Institution. p. 18. ISBN 978-0-89599-014-3.
- Gatesy, J. (1997). "More DNA support for a Cetacea/Hippopotamidae clade: the blood-clotting protein gene gamma-fibrinogen". Molecular Biology and Evolution. 14 (5): 537–543. doi:10.1093/oxfordjournals.molbev.a025790. PMID 9159931.
- Rosenbaum, H. C.; Brownell Jr., R. L.; Schaeff, M. W.B.C.; Portway, V.; White, B. N.; Malik, S.; Pastene, L. A.; Patenaude, N. J.; Baker, C. S.; Goto, M.; Best, P.; Clapham, P. J.; Hamilton, P.; Moore, M.; Payne, R.; Rowntree, V.; Tynan, C. T.; Bannister, J. L.; Desalle, R. (2000). "World-wide genetic differentiation of Eubalaena: Questioning the number of right whale species". Molecular Ecology. 9 (11): 1793–1802. doi:10.1046/j.1365-294x.2000.01066.x. PMID 11091315.
- Cousteau, Jacques; Paccalet, Yves (1986). Whales. H.N. Abrams. OCLC 681455766.
- Bannister 2008, pp. 939–941.
- Fordyce, R. E.; Marx, Felix G. (2012). "The pygmy right whale Caperea marginata: the last of the cetotheres". Proceedings of the Royal Society B. 280 (1753): 20122645. doi:10.1098/rspb.2012.2645. PMC 3574355. PMID 23256199.
- Hassanin, Alexandre; Delsucc, Frédéric; Ropiquet, Anne; Hammere, Catrin; Van Vuurenf, Bettine J.; Mattheef, Conrad; Ruiz-Garcia, Manuel; Catzeflisc, François; Areskough, Veronika; Thanh Nguyena, Trung; Coulouxj, Arnaud (2012). "Histoire évolutive des Cetartiodactyla (Mammalia, Laurasiatheria) racontée par l'analyse des génomes mitochondriaux". Comptes Rendus Biologies (in French). 335 (1): 32–50. doi:10.1016/j.crvi.2011.11.002. PMID 22226162.
- Walker, Matt (2010). "Mediterranean gray whale appears 'back from the dead'". BBC Earth News. Retrieved 21 March 2016.
- Hoare, Philip (2013). "First grey whale spotted south of the Equator". The Guardian. Retrieved 25 January 2016.
- Nakamura, G.; Kato, H. (2014). 日本沿岸域に近年（1990–2005 年）出現したコククジラEschrichtius robustus の骨学的特徴，特に頭骨形状から見た北太平洋西部系群と東部系群交流の可能性 [Possibility of the North Pacific Western group and eastern group exchanges as seen from the osteologic features of the gray whale Eschrichtius robustus recently in the coastal area of Japan (1990–2005), especially from the skull shape] (PDF). 哺乳類科学 (in Japanese). 54 (1): 73–88. doi:10.11238/mammalianscience.54.73.
- Marx, Felix (2010). "The More the Merrier? A Large Cladistic Analysis of Mysticetes, and Comments on the Transition from Teeth to Baleen". Journal of Mammalian Evolution. 18 (2): 77–100. doi:10.1007/s10914-010-9148-4.
- Sasaki, Takeshi; Nikaido, Masato; Hamilton, Healy; Goto, Mutsuo; Kato, Hidehiro; Kanda, Naohisa; Pastene, Luis; Cao, Ying; Fordyce, R.; Hasegawa, Masami; Okada, Norihiro (2005). "Mitochondrial Phylogenetics and Evolution of Mysticete Whales". Systematic Biology. 54 (1): 77–90. doi:10.1080/10635150590905939. PMID 15805012.
- Nikaido, Masato; Hamilton, Healy; Makino, Hitomi (2006). "Baleen Whale Phylogeny and a Past Extensive Radiation Event Revealed by SINE Insertion Analysis". Molecular Biology and Evolution. 23: 7.
- Áranson, Úlfur; Lammers, Fritjof; Kumar, Vikas; Nilsson, Maria (2018). "Whole-genome sequencing of the blue whale and other rorquals finds signatures for introgressive gene flow". Science Advances. 4 (4): 10. doi:10.1126/sciadv.aap9873.
- Bannister 2008, pp. 80–81
- Shorter Oxford English dictionary. Oxford University Press. 2007. p. 3804. ISBN 978-0-19-920687-2.
- Dolin, Eric Jay (2007). Leviathan: The History of Whaling in America. W.W. Norton & Co. p. 22. ISBN 978-0-393-06057-7.
- Potvin, J.; Goldbogen, J. A.; Shadwick, R. E. (2009). "Passive versus active engulfment: verdict from trajectory simulations of lunge-feeding fin whales Balaenoptera physalus". Journal of the Royal Society Interface. 6 (40): 1005–1025. doi:10.1098/rsif.2008.0492. PMC 2827442. PMID 19158011.
- Bannister 2008, p. 80.
- Lockyer, C. (1976). "Body weights of some species of large whales". Journal du Conseil International Pour I'Exploration de la Mer. 36 (3): 259–273. doi:10.1093/icesjms/36.3.259.
- Jones, Mary Lou; Swartz, Steven L.; Leatherwood, Stephen (1984). "A Review of Gray Whale Feeding Ecology". In Jones, Mary Lou; L. Swartz, Steven; Leatherwood, Stephen (eds.). The Gray Whale: Eschrichtius robustus. pp. 33–34, 423–424. ISBN 978-0-12-389180-8.
- Marx, Felix G. (2011). "The More the Merrier? A Large Cladistic Analysis of Mysticetes, and Comments on the Transition from Teeth to Baleen". Journal of Mammalian Evolution. 18 (2): 77–100. doi:10.1007/s10914-010-9148-4.
- Marx, Felix G.; Tsai, Cheng-Hsiu; Fordyce, R. Ewan (2015). "A new Early Oligocene toothed 'baleen' whale (Mysticeti: Aetiocetidae) from western North America: one of the oldest and the smallest". Royal Society Open Science. 2 (12): 150476. Bibcode:2015RSOS....250476M. doi:10.1098/rsos.150476. PMC 4807455. PMID 27019734.
- Deméré, Berta & McGowen 2005
- Steeman, M. E. (2010). "The extinct baleen whale fauna from the Miocene–Pliocene of Belgium and the diagnostic cetacean ear bones". Journal of Systematic Palaeontology. 8 (1): 63–80. doi:10.1080/14772011003594961. OCLC 694418047.
- Marx, Felix G.; Fordyce, R. E. (2015). "Baleen boom and bust: a synthesis of mysticete phylogeny, diversity and disparity". Royal Society Open Science. 2 (4): 140434. Bibcode:2015RSOS....240434M. doi:10.1098/rsos.140434. PMC 4448876. PMID 26064636.
- Jamieson, Barrie G. M. (2016-04-19). Miller, Debra L. (ed.). Reproductive Biology and Phylogeny of Cetaceans. Reproductive Biology and Phylogeny. 7. CRC Press. p. 111. ISBN 978-1-4398-4257-7.
- Fitzgerald, Erich M.G. (2010). "The morphology and systematics of Mammalodon colliveri (Cetacea: Mysticeti), a toothed mysticete from the Oligocene of Australia". Zoological Journal of the Linnean Society. 158 (2): 367–476. doi:10.1111/j.1096-3642.2009.00572.x.
- Fordyce, R. E.; Marx, F. G. (2018). "Gigantism precedes filter feeding in baleen whale evolution". Current Biology. 28 (10): 1670–1676. doi:10.1016/j.cub.2018.04.027. PMID 29754903.
- Deméré, Thomas; Michael R. McGowen; Annalisa Berta; John Gatesy (September 2007). "Morphological and Molecular Evidence for a Stepwise Evolutionary Transition from Teeth to Baleen in Mysticete Whales". Systematic Biology. 57 (1): 15–37. doi:10.1080/10635150701884632. PMID 18266181.
- Vaughan, Terry A.; Ryan, James M.; Czaplewski, Nicholas J. (2011). Mammalogy (5 ed.). Jones and Bartlett Publishers. p. 364. ISBN 978-0-7637-6299-5.
- Peredo, C. M.; Pyenson, N. D.; Marshall, C. D.; Uhe, M. D. (2018). "Tooth Loss Precedes the Origin of Baleen in Whales". Current Biology. 28 (24): 3992–4000.e2. doi:10.1016/j.cub.2018.10.047. PMID 30503622.
- Uhen 2010, pp. 208–210
- Fitzgerald, Erich M. G. (2012). "Archaeocete-like jaws in a baleen whale". Biology Letters. 8 (1): 94–96. doi:10.1098/rsbl.2011.0690. PMC 3259978. PMID 21849306.
- Sanders, A. E.; Barnes, L. G. (2002). "Paleontology of the Late Oligocene Ashley and Chandler Bridge Formations of South Carolina, 3: Eomysticetidae, a new family of primitive mysticetes (Mammalia: Cetacea)". Paleobiology. 93: 313–356.
- Fitzgerald, Erich M. G. (2006). "A bizarre new toothed mysticete (Cetacea) from Australia and the early evolution of baleen whales". Proceedings of the Royal Society. 273 (1604): 2955–2963. doi:10.1098/rspb.2006.3664. PMC 1639514. PMID 17015308.
- Bannister 2008, p. 214.
- Steeman, Mette E.; Hebsgaard, Martin B.; Fordyce, R. E.; Ho, Simon Y. W.; Rabosky, Daniel L.; Nielsen, Rasmus; Rahbek, Carsten; Glenner, Henrik; Sørensen, Martin V.; Willerslev, Eske (2009). "Radiation of Extant Cetaceans Driven by Restructuring of the Oceans". Systematic Biology. 58 (6): 573–585. doi:10.1093/sysbio/syp060. PMC 2777972. PMID 20525610.
- Deméré, Thomas A.; Berta, Annalisa; McGowen, Michael R. (2005). "The taxonomic and evolutionary history of fossil and modern balaenopteroid mysticetes". Journal of Mammalian Evolution. 12 (1): 99–143. doi:10.1007/s10914-005-6944-3.
- Slater, Graham J.; Goldbogen, Jeremy A.; Pyenson, Nicholas D. (2017-05-31). "Independent evolution of baleen whale gigantism linked to Plio-Pleistocene ocean dynamics". Proc. R. Soc. B. 284 (1855): 20170546. doi:10.1098/rspb.2017.0546. ISSN 0962-8452. PMC 5454272. PMID 28539520.
- Goldbogen, J.a.; Cade, D.e.; Calambokidis, J.; Friedlaender, A.s.; Potvin, J.; Segre, P.s.; Werth, A.j. (2017-01-03). "How Baleen Whales Feed: The Biomechanics of Engulfment and Filtration". Annual Review of Marine Science. 9 (1): 367–386. Bibcode:2017ARMS....9..367G. doi:10.1146/annurev-marine-122414-033905. ISSN 1941-1405. PMID 27620830.
- Slater, G. J.; Goldbogen, J. A.; Pyenson, N. D. (2017). "Independent evolution of baleen whale gigantism linked to Plio-Pleistocene ocean dynamics". Proceedings of the Royal Society B: Biological Sciences. 284 (1855): 20170546. doi:10.1098/rspb.2017.0546. PMC 5454272. PMID 28539520.
- Pyenson, Nicholas D. (2017). "The Ecological Rise of Whales Chronicled by the Fossil Record". Current Biology. 27 (11): R558–R564. doi:10.1016/j.cub.2017.05.001. PMID 28586693.
- Marlow, Jeremy R.; Lange, Carina B.; Wefer, Gerold; Rosell-Melé, Antoni (2000-12-22). "Upwelling Intensification As Part of the Pliocene-Pleistocene Climate Transition". Science. 290 (5500): 2288–2291. Bibcode:2000Sci...290.2288M. doi:10.1126/science.290.5500.2288. ISSN 0036-8075. PMID 11125138.
- Bannister 2008, p. 1140.
- Feldhamer 2015, p. 446.
- Dines, James P.; Otárola-Castillo, Erik; Ralph, Peter; Alas, Jesse; Daley, Timothy; Smith, Andrew D.; Dean, Matthew D. (2014). "Sexual selection targets cetacean pelvic bone". Journal of Organic Evolution. 68 (11): 3296–3306. doi:10.1111/evo.12516. PMC 4213350. PMID 25186496.
- "Fin whale". World Wildlife Fund Global. Retrieved 5 March 2016.
- Fox, David (2001). "Balaenoptera physalus (fin whale)". Animal Diversity Web. University of Michigan Museum of Zoology. Retrieved 22 October 2006.
- Vogle, A. W.; Lillie, Margo A.; Piscitelli, Marina A.; Goldbogen, Jeremy A.; Pyenson, Nicholas D.; Shadwick, Robert E. (2015). "Stretchy nerves are an essential component of the extreme feeding mechanism of rorqual whales". Current Biology. 25 (9): 360–361. doi:10.1016/j.cub.2015.03.007. PMID 25942546.
- Goldbogen, Jeremy A. (March–April 2010). "The Ultimate Mouthful: Lunge Feeding in Rorqual Whales". American Scientist. 98 (2): 124–131. doi:10.1511/2010.83.124.
- Pyenson, N. D.; Goldbogen, J. A.; Vogl, A. W.; Szathmary, G.; Drake, R. L.; Shadwick, R. E. (2012). "Discovery of a sensory organ that coordinates lunge-feeding in rorqual whales". Nature. 485 (7399): 498–501. Bibcode:2012Natur.485..498P. doi:10.1038/nature11135. PMID 22622577.
- Tinker 1988, p. 66
- Tinker 1988, p. 50.
- Tinker 1988, p. 51.
- J. Szewciw, L.; de Kerckhove, D. G.; Grime, G. W.; Fudge, D. S. (2010). "Calcification provides mechanical reinforcement to whale baleen α-keratin". Proceedings of the Royal Society B: Biological Sciences. 277 (1694): 2597–2605. doi:10.1098/rspb.2010.0399. PMC 2982044. PMID 20392736.
- Fudge, Douglas S.; Szewciw, Lawrence J.; Schwalb, Astrid N. (2009). "Morphology and Development of Blue Whale Baleen: An Annotated Translation of Tycho Tullberg's Classic 1883 Paper" (PDF). Aquatic Mammals. 35 (2): 226–252. doi:10.1578/AM.35.2.2009.226.
- Bannister 2008, p. 1007.
- Ponganis, Paul J. (2015). Diving Physiology of Marine Mammals and Seabirds. Cambridge University Press. p. 39. ISBN 978-0-521-76555-8.
- Panigada, Simone; Zanardelli, Margherita; Canese, Simonepietro; Jahoda, Maddalena (1999). "How deep can baleen whales dive?" (PDF). Marine Ecology Progress Series. 187: 309–311. Bibcode:1999MEPS..187..309P. doi:10.3354/meps187309.
- Norena, S. R.; Williams, A. M. (2000). "Body size and skeletal muscle myoglobin of cetaceans: adaptations for maximizing dive duration". Comparative Biochemistry and Physiology A. 126 (2): 181–191. doi:10.1016/S1095-6433(00)00182-3. PMID 10936758.
- Nelson, D. L.; Cox, M. M. (2008). Lehninger Principles of Biochemistry (3rd ed.). Worth Publishers. p. 206. ISBN 978-0-7167-6203-4.
- Tinker 1988, p. 69.
- Berne, Robert; Matthew, Levy; Koeppen, Bruce; Stanton, Bruce (2004). Physiology. Elsevier Mosby. p. 276. ISBN 978-0-8243-0348-8.
- Cavendish 2010, p. 99.
- Tinker 1988, p. 70.
- Turgeon, Mary L. (2004). Clinical Hematology: Theory and Procedures. Lippincott Williams & Wilkins. p. 100. ISBN 978-0-7817-5007-3.
- Cavendish 2010, p. 101.
- Cavendish 2010, pp. 93–94.
- Bunn, James H. (2014). The Natural Law of Cycles. Transaction Publishers. p. 314. ISBN 978-1-4128-5187-9.
- Mosbergen, Dominique (2014). "Sleeping Humpback Whale Captured In Rare Footage". Huffington Post. Retrieved 23 January 2016.
- Reidenberg, J. S.; Laitman, J. T. (2007). "Discovery of a low frequency sound source in Mysticeti (baleen whales): anatomical establishment of a vocal fold homolog". The Anatomical Record. 290 (6): 745–759. doi:10.1002/ar.20544. PMID 17516447.
- Cavendish 2010, p. 95.
- "Appendix H: Marine Mammal Hearing and Sensitivity to Acoustic Impacts" (PDF). Atlantic G&G Programmatic EIS. p. H-4, § Hearing in Mysticete Cetaceans.
- Cavendish 2010, p. 96.
- Yamato, Maya; Ketten, Darlene R.; Arruda, Julie; Cramer, Scott; Moore, Kathleen (2012). "The Auditory Anatomy of the Minke Whale (Balaenoptera acutorostrata): A Potential Fatty Sound Reception Pathway in a Baleen Whale". The Anatomical Record. 295 (6): 991–998. doi:10.1002/ar.22459. PMC 3488298. PMID 22488847.
- Cavendish 2010, p. 94.
- Feng, Ping; Zheng, Jinsong; Rossiter, Stephen J.; Wang, Ding; Zhao, Huabin (2014). "Massive losses of taste receptor genes in toothed and baleen whales". Genome Biology and Evolution. 6 (6): 1254–65. doi:10.1093/gbe/evu095. PMC 4079202. PMID 24803572.
- Lockyer, C. J. H.; Brown, S. G. (1981). "The Migration of Whales". In Aidley, D. (ed.). Animal Migration. CUP Archive. p. 111. ISBN 978-0-521-23274-6.
- Lee, Jane J. (2015). "A Gray Whale Breaks The Record For Longest Mammal Migration". National Geographic. Retrieved 23 January 2016.
- Kellogg, Remington C.; Whitmore, Jr., Frank (1957). "Marine Mammals". Geological Society of America Memoirs. 1 (67): 1223–1224. doi:10.1130/MEM67V1-p1223.
- Bannister 2008, pp. 357–361.
- Croll, Donald A.; Marinovic, Baldo; Benson, Scott; Chavez, Francisco P.; Black, Nancy; Ternullo, Richard; Tershy, Bernie R. (2005). "From wind to whales:: trophic links in a coastal upwelling system". Marine Ecology Progress Series. 289: 117–130. doi:10.3354/meps289117. JSTOR 24867995.
- Sanders, Jon G.; Beichman, Annabel C.; Roman, Joe; Scott, Jarrod J.; Emerson, David; McCarthy, James J.; Girguis, Peter R. (2015). "Baleen whales host a unique gut microbiome with similarities to both carnivores and herbivores". Nature Communications. 6: 8285. Bibcode:2015NatCo...6.8285S. doi:10.1038/ncomms9285. PMC 4595633. PMID 26393325.
- Potvin, J.; Goldbogen, J.A.; Shadwick, R.E. (2010). "Scaling of lunge feeding in rorqual whales: An integrated model of engulfment duration". Journal of Theoretical Biology. 267 (3): 437–453. doi:10.1016/j.jtbi.2010.08.026. PMID 20816685.
- Laidre, Kristin L.; Heide-Jørgensen, Mads Peter; Nielsen, Torkel Gissel (2007). "Role of the bowhead whale as a predator in West Greenland". Marine Ecology Progress Series. 346: 285–297. Bibcode:2007MEPS..346..285L. doi:10.3354/meps06995. JSTOR 24871544.
- Steele, John H. (1970). "Feeding pattern of baleen whales in the ocean". Marine Food Chains. University of California Press. pp. 245–247. ISBN 978-0-520-01397-1.
- Goldbogen, J. A.; Calambokidis, J.; Oleson, E.; Potvin, J.; Pyenson, N. D.; Schorr, G.; Shadwick, R. E. (2011). "Mechanics, hydrodynamics and energetics of blue whale lunge feeding: efficiency dependence on krill density". Journal of Experimental Biology. 214 (Pt 1): 131–146. doi:10.1242/jeb.048157. PMID 21147977.
- Bannister 2008, pp. 806–813.
- Goldbogen, J. A.; Calambokidis, J.; Oleson, E.; Potvin, J.; Pyenson, N. D.; Schorr, G.; Shadwick, R. E. (2011-01-01). "Mechanics, hydrodynamics and energetics of blue whale lunge feeding: efficiency dependence on krill density". Journal of Experimental Biology. 214 (1): 131–146. doi:10.1242/jeb.048157. ISSN 0022-0949. PMID 21147977.
- Potvin, Jean; Werth, Alexander J. (2017-04-11). "Oral cavity hydrodynamics and drag production in Balaenid whale suspension feeding". PLOS ONE. 12 (4): e0175220. Bibcode:2017PLoSO..1275220P. doi:10.1371/journal.pone.0175220. ISSN 1932-6203. PMC 5388472. PMID 28399142.
- Kenney, Robert D.; Hyman, Martin A. M.; Owen, Ralph E.; Scott, Gerald P.; Winn, Howard E. (1986-01-01). "Estimation of Prey Densities Required by Western North Atlantic Right Whales". Marine Mammal Science. 2 (1): 1–13. doi:10.1111/j.1748-7692.1986.tb00024.x. ISSN 1748-7692.
- Laidre, KL; Heide-Jørgensen, MP; Nielsen, TG (2007-09-27). "Role of the bowhead whale as a predator in West Greenland". Marine Ecology Progress Series. 346: 285–297. Bibcode:2007MEPS..346..285L. doi:10.3354/meps06995. ISSN 0171-8630.
- Ferguson, Steven H.; Higdon, Jeff W.; Westdal, Kristin H. (2012). "Prey items and predation behavior of killer whales (Orcinus orca) in Nunavut, Canada based on Inuit hunter interviews". Aquatic Biosystems. 8 (3): 3. doi:10.1186/2046-9063-8-3. PMC 3310332. PMID 22520955.
- Ford, John K. B.; Reeves, Randall R. (2008). "Fight or flight: antipredator strategies of baleen whales". Mammal Review. 38 (1): 50–86. CiteSeerX 10.1.1.573.6671. doi:10.1111/j.1365-2907.2008.00118.x.
- Dicken, M. L.; Kock, A. A.; Hardenberg, M. (2014). "First observations of dusky sharks (Carcharhinus obscurus) attacking a humpback whale (Megaptera novaeangliae) calf". Marine and Freshwater Research. 66 (12): 1211–1215. doi:10.1071/MF14317.
- Martin, R.A. "Squaliformes Dogfish Sharks". ReefQuest Centre for Shark Research. Retrieved 24 January 2016.
- Bannister 2008, p. 85.
- Feldhamer 2015, p. 457.
- Nogata, Yasuyuki; Matsumura, Kiyotaka (2006). "Larval development and settlement of a whale barnacle". Biology Letters. 2 (1): 92–93. doi:10.1098/rsbl.2005.0409. PMC 1617185. PMID 17148335.
- Busch, Robert (1998). Gray Whales: Wandering Giants. Orca Book Publishing. p. 62. ISBN 978-1-55143-114-7.
- Ólafsdóttir, Droplaug; Shinn, Andrew P. (2013). "Epibiotic macrofauna on common minke whales, Balaenoptera acutorostrata Lacépède, 1804, in Icelandic waters". Parasites & Vectors. 6 (105): 105. doi:10.1186/1756-3305-6-105. PMC 3673810. PMID 23594428.
- Bannister 2008, pp. 86–87
- W. Rice, D. (1977). "Synopsis of biological data on the sei whale and Bryde's whale in the eastern North Pacific". Report of the International Whaling Commission. Special Issue 1: 92–97.
- Aguilar, A.; Lockyer, C. H. (1987). "Growth, physical maturity, and mortality of fin whales (Balaenoptera physalus) inhabiting the temperate waters of the northeast Atlantic". Canadian Journal of Zoology. 65 (2): 253–264. doi:10.1139/z87-040.
- Ohsumi, S. (1977). "Bryde's whales in the pelagic whaling ground of the North Pacific". Report of the International Whaling Commission: 140–9.
- Horwood, Joseph W. (1990). Biology and Exploitation of the Minke Whale. CRC Press. pp. 72–80. ISBN 978-0-8493-6069-5.
- Fortune, Sarah M. E.; Trites, Andrew W.; Perryman, Wayne L.; Moore, Michael J.; Pettis, Heather M.; Lynn, Morgan S. (2012). "Growth and rapid early development of North Atlantic right whales (Eubalaena glacialis)". Journal of Mammalogy. 93 (5): 1342–1354. doi:10.1644/11-MAMM-A-297.1.
- A.R. Knowlton, S.D. Kraus and R.D. Kenney (1994). "Reproduction in North Atlantic right whales (Eubalaena glacialis)". Canadian Journal of Zoology. 72 (7): 1297–1305. doi:10.1139/z94-173.CS1 maint: uses authors parameter (link)
- Duffus, John H.; Templeton, Douglas M.; Nordberg, Monica (2009). Concepts in Toxicology. Royal Society of Chemistry. p. 171. doi:10.1039/9781847559753-00013. ISBN 978-0-85404-157-2.
- Gardner, David (2007). "Whale survives harpoon attack 130 years ago to become 'world's oldest mammal'". Daily Mail. Retrieved 6 January 2016.
- Berta, Annalisa (2012). Return to the Sea: The Life and Evolutionary Times of Marine Mammals. University of California Press. p. 121. ISBN 978-0-520-27057-2.
- Evans, Peter G. H.; Raga, Juan A. (2001). Marine Mammals: Biology and Conservation. Plenum Publishers. pp. 221–223. ISBN 978-0-306-46573-4.
- Cavendish 2010, p. 102.
- Glenday, Craig (2015-09-01). Longest animal penis. Guinness World Records. ISBN 978-1-910561-02-7.
the longest penis belongs to the blue whale at up to 2.4 m (8 ft)
- Anitei, Stefan (2007). "The Largest Penis in the World – Both for humans and animals, size does matter". Softpedia. Retrieved 15 March 2016.
- Feldhamer, George A.; Thompson, Bruce C.; Chapman, Joseph A. (2003). Wild mammals of North America : biology, management, and conservation (2nd ed.). Johns Hopkins University Press. p. 432. ISBN 978-0-8018-7416-1.
- Bannister 2008, pp. 85–86
- Butti, C.; Sherwood, C. C.; Hakeem, A. Y.; M. Allman, J.; Hof, P. R. (2009). "Total number and volume of Von Economo neurons in the cerebral cortex of cetaceans". The Journal of Comparative Neurology. 515 (2): 243–259. doi:10.1002/cne.22055. PMID 19412956.
- "Rock art hints at whaling origins". BBC News. 2004. Retrieved 25 January 2016.
Stone Age people may have started hunting whales as early as 6,000 BC, new evidence from South Korea suggests.
- Marrero, Meghan E.; Thornton, Stuart (2011). "Big Fish: A Brief History of Whaling". National Geographic. Retrieved 25 January 2016.
- Ford, Catherine (2015). "A Savage History: Whaling in the South Pacific and Southern Oceans". The Monthly. Retrieved 21 April 2016.
- Proulx, J.P. (1993). Basque whaling in Labrador in the 16th century. National Historic Sites, Parks Service, Environment Canada. pp. 260–286. ISBN 978-0-660-14819-9. ISSN 0821-1027.
- "Whale products". New Bedford Whaling Museum. Retrieved 25 January 2016.
- Stonehouse, Bernard (2007). "British Arctic whaling: an overview". University of Hull. Retrieved 25 January 2016.
- Tonnessen, J. N.; Johnsen, A.O (1982). The History of Modern Whaling. The University of California Press. pp. 220, 549. ISBN 978-0-520-03973-5.
- McNeill, J. R. (2000). "Whaling and Fishing". Something New Under the Sun: An Environmental History of the 20th Century. W. W. Norton and Company, Inc. pp. 128–130. ISBN 978-0-393-04917-6.
- Beckman, Daniel (2013). "Conservation of Cetaceans". Marine Environmental Biology and Conservation. Jones and Bartlett Learning. p. 328. ISBN 978-0-7637-7350-2.
- International Whaling Commission Schedule, paragraph 10(e). International Whaling Commission.
- "Keyword search: Baleen whales". The IUCN Red List of Threatened species. Version 2013.1. IUCN. Retrieved 17 July 2013.
- Elliot, Wendy (2007). Whales in Hot Water? (PDF). World Wildlife Fund. pp. 9–10. Archived from the original (PDF) on 2016-04-05.
- Black, Richard (2009). "Whale watching 'worth billions'". BBC News. Retrieved 27 January 2016.
- Barnes, R. H. (1996). "Lamakera, Solor. Ethnographic Notes on a Muslim Whaling Village of Eastern Indonesia". Anthropos. 91 (91): 75–88. JSTOR 40465273.
- O'Connor, S.; Campbell, R.; Cortez, H.; Knowles, T. (2009). "Whale Watching and Whaling". Whale Watching Worldwide: tourism numbers, expenditures and expanding economic benefits (PDF) (Report). International Fund for Animal Welfare. pp. 9–12.
- Clifford, Frank (1994). "Gray Whale Removed From Endangered List". LA Times. Retrieved 27 January 2016.
- White, Doc (2010). "Southern Right Whale". In Fitzpatrick, Lisa (ed.). Defying Extinction – Partnerships to Safeguard Global Biodiversity. Earth in Focus. p. 7. ISBN 978-0-9841686-5-1.
- "IUCN Species of the Day: North Atlantic Right Whale". Bush Warriors. 2010. Retrieved 27 January 2016.
- "Commercial Whaling". International Whaling Commission. Retrieved 30 January 2016.
- "Scientific Permit Whaling". International Whaling Commission. Retrieved 29 January 2016.
- H. Schofield, Clive; Lee, Seokwoo; Kwon, Moon-Sang, eds. (2014). "Whaling in the Antarctic: Protecting Rights in Areas Beyond National Jurisdiction Through International Litigation". Limits of Maritime Jurisdiction. Brill. p. 527. ISBN 978-90-04-26258-4.
- "Japan and whaling". Greenpeace International. Retrieved 29 January 2016.
- Gales, Nicholas J.; Kasuya, Toshio; Clapham, Phillip J.; Brownell, Jr, Robert L. (2005). "Japan's whaling plan under scrutiny". Nature. 435 (7044): 883–884. Bibcode:2005Natur.435..883G. doi:10.1038/435883a. PMID 15959491.
- Tabuchi, Hiroko; Simons, Marlise (2014). "U.N. Court Orders Japan to Halt Whaling Off Antarctica". NY Times. Retrieved 29 January 2016.
- "Japan to resume whaling in Antarctic despite court ruling". BBC News. Associated Press. 2015. Retrieved 29 January 2016.
- Vanderlaan, Angelia S. M.; Taggart, Christopher T. (2007). "Vessel Collisions with Whales: The Probability of Lethal Injury Based on Vessel Speed". Marine Mammal Science. 23 (1): 144–156. doi:10.1111/j.1748-7692.2006.00098.x.
- Silber, G. K.; Adams, J. D.; Fonnesbeck, C. J. (2014). "Compliance with vessel speed restrictions to protect North Atlantic right whales". PeerJ. 2: e399. doi:10.7717/peerj.399. PMC 4060020. PMID 24949229.
- Melcón, Mariana L.; Cummins, Amanda J.; Kerosky, Sara M.; Roche, Lauren K.; Wiggins, Sean M.; Hildebrand, John A. (2012). "Blue Whales Respond to Anthropogenic Noise". PLoS ONE. 7 (2): e32681. Bibcode:2012PLoSO...732681M. doi:10.1371/journal.pone.0032681. PMC 3290562. PMID 22393434.
- Reeves, Randal R.; Clapham, P.J. L.; Brownell, R.; K., Silber G. (1998). Recovery plan for the blue whale (Balaenoptera musculus) (PDF). National Marine Fisheries Service. p. 42.
- O'Shea, Thomas J.; Brownell, Jr., Robert L. (1994). "Organochlorine and metal contaminants in baleen whales: a review and evaluation of conservation implications". Science of the Total Environment. 154 (3): 179–200. Bibcode:1994ScTEn.154..179O. doi:10.1016/0048-9697(94)90087-6. PMID 7973606.
- "North Atlantic Right Whale (Eubalaena glacialis)". Office of Protected Resources. NOAA Fisheries. Retrieved 15 December 2016.
- "Cetaceans" (PDF). Entanglement of Marine Species in Marine Debris with an Emphasis on Species in the United States. NOAA Marine Debris Report. 2014. pp. 9–10.
- Perry, Tony (1998). "J.J. The Gray Whale Going To Sea – Rescued Orphan Calf Will Be Freed This Week". Seattle Times. Retrieved 29 January 2016.
- Hubbs, Carl L.; Evans, E. William (1974). "The California gray whale : papers presented at the California Gray Whale Workshop, Scripps Institution of Oceanography". Marine Fisheries Review. 36 (4): 1–74. doi:10.5962/bhl.title.4029.
- Sumich, J. L.; Goff, T.; Perryman, W. L. (2001). "Growth of two captive gray whale calves" (PDF). Aquatic Mammals. 27 (3): 231–233.
- Perry, Tony (1998). "Rescued Whale J.J. Begins Long Journey Home". LA Times. Retrieved 29 January 2016.
- Kimura, S.; Nemoto, T. (1956). "Note on a minke whale kept alive in aquarium". Scientific Reports of the Whales Research Institute. 11: 181–189.
- Bannister, John L. (2008). "Baleen Whales (Mysticetes)". In F. Perrin, William; Würsig, Bernd; Thewissen, J. G. M. (eds.). Encyclopedia of Marine Mammals (2 ed.). Academic Press. pp. 80–89. ISBN 978-0-12-373553-9.
- Cavendish, Marshall (2010). "Gray whale". Mammal Anatomy: An Illustrated Guide. Marshall Cavendish Corporation. ISBN 978-0-7614-7882-9.
- Cope, E. D. (1891). "Syllabus of Lectures on Geology and Paleontology". Ferris Brothers. p. 69. OCLC 31419733.
- Deméré, T. A.; Berta, A.; McGowen, M. R. (2005). "The taxonomic and evolutionary history of fossil and modern balaenopteroid mysticetes". Journal of Mammalian Evolution. 12 (1): 99–143. doi:10.1007/s10914-005-6944-3. OCLC 264019292.
- Feldhamer, George A.; Drickamer, Lee; Vessey, Stephen C.; Merritt, Joseph H.; Krajewski, Carey F. (2015). "Cetacea". Mammalogy: Adaptation, Diversity, Ecology. Johns Hopkins University Press. ISBN 978-1-4214-1588-8.
- Rice, Dale W. (1998). "Marine mammals of the world: systematics and distribution". Society for Marine Mammalogy: 1–231. OCLC 40622084.
- Tinker, Spencer W. (1988). Whales of the World. Brill Archive. ISBN 978-0-935848-47-2.
- Uhen, M. D. (2010). "The Origin(s) of Whales". Annual Review of Earth and Planetary Sciences. 38 (1): 189–219. Bibcode:2010AREPS..38..189U. doi:10.1146/annurev-earth-040809-152453.