Waharoa Temporal range: Late Oligocene, | |
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Holotype skull shown from above | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Mammalia |
Order: | Artiodactyla |
Infraorder: | Cetacea |
Family: | † Eomysticetidae |
Genus: | † Waharoa Boessenecker and Fordyce, 2015 |
Species: | †W. ruwhenua |
Binomial name | |
†Waharoa ruwhenua Boessenecker and Fordyce, 2015 | |
Waharoa is a genus of eomysticetid baleen whale from the Late Oligocene (Chattian) of New Zealand. It was identified with the discovery of Waharoa ruwhenua by Boessenecker and Fordyce (2015), which added a new genus and species to a monophyletic family Eomysticetidae. [1]
Boessenecker and Fordyce (2015) characterize the species as follows: "Waharoa ruwhenua shares Tohoraata and Tokarahia dorsoventrally shallow and wide occipital condyles, a triangular anterior process and well-developed incisural flange of the periotic; with Tohoraata and Tokarahia a concave anterodorsal margin of the anterior process of the periotic and a smooth and transversely convex posterior bullar facet; with Tohoraata a distinct lateral tubercle on the anterior process; and with Eomysticetus and Micromysticetus a short posterior process". [1]
Waharoa ruwhenua had a rostrum that was less flexible than those of modern edentulous mysticetes, yet much more flexible than the rostra of toothed mysticetes. [1] This intermediate flexibility suggests that W. ruwhenua harbored the most primitive form of a kinetic rostrum in the Mysticeti.
Waharoa ruwhenua had sulci and palatal foramina localized to the posterior half of the palate and lacked these features anteriorly, suggesting that baleen was only present in the posterior palatal regions. [1] The posterior localization of baleen along with a delicate temporomandibular joint with a probable synovial capsule, an anteroposteriorly expanding palate, a non-laterally deflected coronoid process, and a shortage of characteristics indicative of lunge feeding indicate that W. ruwhenua could have utilized skim filter-feeding like modern Balaenidae to feed for zooplankton.
The hypothesis that W. rewhenua was a skim feeder suggests that skim filter-feeding may have been the earliest form of feeding in the edentulous Chaeomysticeti clade. [1]
Based on the enlarged temporal fossae and enlarged mandibular canal, Waharoa was probably incapable of lunge-feeding, although it remains unclear whether it could skim-feed or filter prey in the benthic zone. Waharoa shared its habitat with the odontocetes Awamokoa , Austrosqualodon , Otekaikea , and Waipatia , and the mysticetes Horopeta , Matapanui , Mauicetus , Tohoraata , Tokarahia , and Whakakai .
Baleen whales, also known as whalebone whales, are marine mammals of the parvorder Mysticeti in the infraorder Cetacea, which use keratinaceous baleen plates in their mouths to sieve planktonic creatures from the water. Mysticeti comprises the families Balaenidae, Balaenopteridae (rorquals), Eschrichtiidae and Cetotheriidae. There are currently 16 species of baleen whales. While cetaceans were historically thought to have descended from mesonychians, molecular evidence instead supports them as a clade of even-toed ungulates (Artiodactyla). Baleen whales split from toothed whales (Odontoceti) around 34 million years ago.
Baleen is a filter-feeding system inside the mouths of baleen whales. To use baleen, the whale first opens its mouth underwater to take in water. The whale then pushes the water out, and animals such as krill are filtered by the baleen and remain as a food source for the whale. Baleen is similar to bristles and consists of keratin, the same substance found in human fingernails, skin and hair. Baleen is a skin derivative. Some whales, such as the bowhead whale, have longer baleen than others. Other whales, such as the gray whale, only use one side of their baleen. These baleen bristles are arranged in plates across the upper jaw of whales.
Mammalodon is an extinct genus of archaic baleen whale belonging to the family Mammalodontidae.
Aetiocetus is a genus of extinct basal mysticete, or baleen whale that lived 33.9 to 23.03 million years ago, in the Oligocene in the North Pacific ocean, around Japan, Mexico, and Oregon, U.S. It was first described by Douglas Emlong in 1966 and currently contains known four species, A. cotylalveus, A. polydentatus, A. tomitai, and A. weltoni. These whales are remarkable for their retention of teeth and presence of nutrient foramina, indicating that they possessed baleen. Thus, Aetiocetus represents the transition from teeth to baleen in Oligocene mysticetes. Baleen is a highly derived character, or synapomorphy, of mysticetes, and is a keratinous structure that grows from the palate, or roof of the mouth, of the whale. The presence of baleen is inferred from the fossil record in the skull of Aetiocetus. Aetiocetus is known from both sides of the Pacific Ocean: it was first documented in Oregon, United States, but it is also known from Japan and Mexico. The genus is currently constrained to the Northern hemisphere and has little value in biostratigraphic studies of the Oligocene due to its limited occurrences across the Pacific.
Cetotheriidae is a family of baleen whales. The family is known to have existed from the Late Oligocene to the Early Pleistocene before going extinct. Although some phylogenetic studies conducted by Fordyce & Marx 2013 recovered the living pygmy right whale as a member of Cetotheriidae, making the pygmy right whale the only living cetotheriid, other authors either dispute this placement or recover Neobalaenidae as a sister group to Cetotheriidae.
The Kokoamu Greensand is a geological formation found in New Zealand. It is a fossil-bearing, late Oligocene, greensand rock unit of the eastern South Island, especially the Waitaki District of North Otago and the southern Canterbury region. The formation was named by geologist Maxwell Gage in the 1950s. In North Otago it underlies the thicker and harder Otekaike Limestone. The formation gets its green colour from the mineral glauconite which forms slowly on the ocean floor.
Eomysticetus is an extinct genus of baleen whale from the late Oligocene (Chattian) Chandler Bridge Formation of South Carolina.
Llanocetus is a genus of extinct toothed baleen whales from the Late Eocene of Antarctica. The type species, Llanocetus denticrenatus, reached gigantic proportions, with the juvenile specimen reaching an estimated 8 m (26 ft) in length; a second, unnamed species, known only from three isolated premolar teeth, reached an estimated total body length of up to 12 m (39 ft). Like other contemporary baleen whales of the Eocene, Llanocetus completely lacked baleen in its jaws. It was probably a suction feeder like the modern beaked and pygmy right whales.
Otekaikea is an extinct genus of toothed whale closely related to Waipatia. It is known from the late Oligocene (Chattian) of New Zealand.
Mauicetus is a genus of extinct baleen whale from the Late Oligocene of New Zealand.
Eomysticetidae is a family of extinct mysticetes belonging to Chaeomysticeti. It is one of two families in the basal chaeomysticete clade Eomysticetoidea.
Tokarahia is a genus of eomysticetid baleen whale from the Late Oligocene (Chattian) of New Zealand. There are two recognized species, T. kauaeroa and T. lophocephalus.
Aetiocetidae is an extinct family of toothed baleen whales known from the Oligocene and latest Eocene, so far only from rocks deposited in the North Pacific Ocean. The whales ranged in size from 3 to 8 metres long. Many of the described specimens were discovered from the Upper Oligocene of the Japanese Morawan Formation, the largest known one from the Morawan's Upper tuffaceous siltstone. Other formally described extinct toothed mysticetis from this time are smaller, from 3 to 4 metres in length. Mysticeti with true baleen are seen in fossils from the Upper Oligocene. The monophyly of the family is still uncertain, as are the evolutionary relationship between the early toothed baleen whales and the early and extant edentulous baleen whales. However, the cladistic analyses of Coronodon and Mystacodon seem to indicate that Aetiocetidae and Llanocetidae are more closely related to crown Mysticeti than to Mammalodontidae, Coronodon, and Mystacodon.
Matapanui is a genus of eomysticetid baleen whale from the Late Oligocene Kokoamu Greensand of New Zealand.
Horopeta is a genus of baleen whale from the Late Oligocene (Chattian) Kokoamu Greensand of New Zealand.
Coronodon is a genus of toothed (transitional) baleen whales from the Early Oligocene Ashley and Chandler Bridge formations of South Carolina. The genus contains three species: the type species C. havensteini, and additional species C. newtonorum and C. planifrons.
Whakakai is a genus of baleen whale from the Late Oligocene (Chattian) Kokoamu Greensand of New Zealand.
Sitsqwayk is a genus of baleen whale from Late Oligocene (Chattian) marine deposits in Washington state. The generic name refers to a powerful water spirit in the folklore of the Klallam that is said to bring wealth.
Fucaia is an extinct genus of primitive baleen whale belonging to the family Aetiocetidae that is known from Oligocene and latest Eocene marine deposits on Vancouver Island, Canada, the Olympic Peninsula, Washington State, and Oregon.
Toipahautea is a genus of baleen whale from the Late Oligocene (Chattian) Kokoamu Greensand of New Zealand.