Sphenopalatine vacuities

Last updated February 23, 2019

In rodents, sphenopalatine vacuities are perforations of the roof of the mesopterygoid fossa, the open space behind the palate, in between the parapterygoid fossae.^[1] They may perforate the presphenoid or basisphenoid bone.^[2] Their development and form are variable between and within species, and features of the sphenopalatine vacuities have been used as characters in cladistic analyses.^[3]

Rodents are mammals of the order Rodentia, which are characterized by a single pair of continuously growing incisors in each of the upper and lower jaws. About 40% of all mammal species are rodents ; they are found in vast numbers on all continents except Antarctica. They are the most diversified mammalian order and live in a variety of terrestrial habitats, including human-made environments.

The palate is the roof of the mouth in humans and other mammals. It separates the oral cavity from the nasal cavity. A similar structure is found in crocodilians, but in most other tetrapods, the oral and nasal cavities are not truly separate. The palate is divided into two parts, the anterior bony hard palate and the posterior fleshy soft palate.

Cladistics is an approach to biological classification in which organisms are categorized in groups ("clades") based on the most recent common ancestor. Hypothesized relationships are typically based on shared derived characteristics (synapomorphies) that can be traced to the most recent common ancestor and are not present in more distant groups and ancestors. A key feature of a clade is that a common ancestor and all its descendants are part of the clade. Importantly, all descendants stay in their overarching ancestral clade. For example, if within a strict cladistic framework the terms animals, bilateria/worms, fishes/vertebrata, or monkeys/anthropoidea would be used, these terms would include humans. Many of these terms are normally used paraphyletically, outside of cladistics, e.g. as a 'grade'. Radiation results in the generation of new subclades by bifurcation.

Among Oryzomyini, a mainly South American group, a 2006 study distinguished three character states—large, wide vacuities, as among others in Oligoryzomys and Holochilus ; small, narrow vacuities, as among others in Lundomys and Nephelomys ; and no or vestigial vacuities, as among others in Mindomys and Oryzomys .^[2] Phyllotini all have very large sphenopalatine vacuities, as does Sigmodon. The vacuities in Reithrodon , formerly considered a phyllotine, are especially large.^[4] Nyctomys is special in having sphenopalatine vacuities restricted to the basisphenoid bone.^[2] Character polarity for the development of the vacuities in Cricetidae is difficult to determine, but their absence may be primitive in the Neotominae.^[4]

Oryzomyini, or rice rat, is a tribe of rodents in the subfamily Sigmodontinae of family Cricetidae. It includes about 120 species in about thirty genera, distributed from the eastern United States to the southernmost parts of South America, including many offshore islands. It is part of the clade Oryzomyalia, which includes most of the South American Sigmodontinae.

Oligoryzomys is a genus of rodents in the tribe Oryzomyini of family Cricetidae. Many species are known as pygmy rice rats or colilargos. The genus is found from Mexico to Tierra del Fuego and includes about 17 species.

Holochilus is a genus of semiaquatic rodents in the tribe Oryzomyini of family Cricetidae, sometimes called marsh rats. It contains three living species, H. brasiliensis, H. chacarius, and H. sciureus, which are widely distributed in South America east of the Andes. A fourth species from the Pleistocene of Bolivia was formerly classified as H. primigenus, but is now placed in the genus Reigomys.

The development of sphenopalatine vacuities has also been used to distinguish among members of the Sciurini group of squirrels.^[5]

Sciurini is a tribe that includes about forty species of squirrels, mostly from the Americas. It includes five living genera—the American dwarf squirrels, Microsciurus; the Bornean Rheithrosciurus; the widespread American and Eurasian tree squirrels of the genus Sciurus, which includes some of the best known squirrel species; the Central American Syntheosciurus; and the American pine squirrels, Tamiasciurus. Like other arboreal squirrels, they are sometimes referred to as tree squirrels.

Squirrels are members of the family Sciuridae, a family that includes small or medium-size rodents. The squirrel family includes tree squirrels, ground squirrels, chipmunks, marmots, flying squirrels, and prairie dogs amongst other rodents. Squirrels are indigenous to the Americas, Eurasia, and Africa, and were introduced by humans to Australia. The earliest known squirrels date from the Eocene period and are most closely related to the mountain beaver and to the dormouse among other living rodent families.

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Euryoryzomys emmonsae, also known as Emmons' rice rat or Emmons' oryzomys, is a rodent from the Amazon rainforest of Brazil in the genus Euryoryzomys of the family Cricetidae. Initially misidentified as E. macconnelli or E. nitidus, it was formally described in 1998. A rainforest species, it may be scansorial, climbing but also spending time on the ground. It lives only in a limited area south of the Amazon River in the state of Pará, a distribution that is apparently unique among the muroid rodents of the region.

Lundomys molitor, also known as Lund's amphibious rat or the greater marsh rat, is a semiaquatic rat species from southeastern South America.

Irenomys tarsalis, also known as the Chilean climbing mouse, Chilean tree mouse, or long-footed irenomys, is a rodent found in Chile, from about 36° to 46°S, and in adjacent Argentina, mainly in forests. It is a large, long-tailed, soft-furred mouse characterized by grooved upper incisors and specialized molars with transverse ridges, divided by deep valleys, which are connected by a transverse ridge along the midline of the molars.

Nephelomys albigularis, also known as the white-throated oryzomys or Tomes's rice rat, is a species of rodent in the genus Nephelomys of family Cricetidae. Described in 1860, it was the first Nephelomys species to be discovered. It was originally described in the defunct genus Hesperomys as Hesperomys albigularis and considered related to the much smaller H. longicaudatus. By 1894, it was placed in Oryzomys, as Oryzomys albigularis, and associated with what is now Nephelomys meridensis. In the early 1960s, the scope of the species was considerably expanded to include most of the species that are now in Nephelomys, as well as a single name, boliviae, that is currently a synonym of Euryoryzomys nitidus. From 1976 on, several of these were reinstated as separate species.

<i>Oryzomys gorgasi</i> A rodent in the family Cricetidae from northwestern Columbia and Venezuela

Oryzomys gorgasi, also known as Gorgas's oryzomys or Gorgas's rice rat, is a rodent in the genus Oryzomys of family Cricetidae. First collected as a living animal in 1967, it is known from only a few localities, including a freshwater swamp in the lowlands of northwestern Colombia and a mangrove islet in northwestern Venezuela. It formerly occurred on the island of Curaçao off northwestern Venezuela; this extinct population has been described as a separate species, Oryzomys curasoae, but does not differ morphologically from mainland populations.

Mindomys hammondi, also known as Hammond's rice rat or Hammond's oryzomys, is a species of rodent in the tribe Oryzomyini of family Cricetidae. Formerly considered to be related with Nectomys, Sigmodontomys, Megalomys, or Oryzomys, it is now placed in its own genus, Mindomys, but its relationships remain obscure; some evidence supports a placement near Oecomys or as a basal member of Oryzomyini.

Eremoryzomys polius, also known as the gray rice rat or the Marañon oryzomys, is a rodent species in the tribe Oryzomyini of the family Cricetidae. Discovered in 1912 and first described in 1913 by Wilfred Osgood, it was originally placed in Oryzomys and named Oryzomys polius. In 2006, a cladistic analysis found that it was not closely related to Oryzomys in the strict sense or to any other oryzomyine then known, so that it is now placed in its own genus, Eremoryzomys. The Brazilian genus Drymoreomys, named in 2011, is probably the closest relative of Eremoryzomys. Eremoryzomys has a limited distribution in the dry upper valley of the Marañón River in central Peru, but may yet contain more than one species.

Sigmodontomys is a genus of rodent in the tribe Oryzomyini of family Cricetidae. It is related to Nectomys and Melanomys and used to be included in Nectomys. It includes two species, Sigmodontomys alfari and the much rarer Sigmodontomys aphrastus, but whether these are indeed each other's closest relatives is uncertain.

Transandinomys is a genus of rodents in the tribe Oryzomyini of family Cricetidae. It includes two species—T. bolivaris and T. talamancae—found in forests from Honduras in Central America south and east to southwestern Ecuador and northwestern Venezuela in northern South America. Until 2006, its members were included in the genus Oryzomys, but phylogenetic analysis showed that they are not closely related to the type species of that genus, and they have therefore been placed in a new genus. They may be most closely related to genera like Hylaeamys and Euryoryzomys, which contain very similar species. Both species of Transandinomys have had eventful taxonomic histories.

Nephelomys is a genus of South American oryzomyine rodents found in the Andes from Bolivia to Venezuela, with a westward extension into the mountains of Costa Rica. Its generic name is derived from the Ancient Greek word nephelê "mist", referring to the cloud forest habitat of the members of the genus.

In anatomy, posterolateral palatal pits are gaps at the sides of the back of the bony palate, near the last molars. Posterolateral palatal pits are present, in various degrees of development, in several members of the rodent family Cricetidae. Many members of the family lack them or have only simple pits, but Arvicolinae and Oryzomyini have more highly developed posterolateral palatal pits. Posterolateral palatal pits are also present in some other rodents, including Glis, Jaculus, Hystrix, Abrocoma, Ctenomys, Chinchilla, and Lagidium.

In rodent anatomy, the zygomatic plate is a bony plate derived from the flattened front part of the zygomatic arch (cheekbone). At the back, it connects to the front (maxillary) root of the zygomatic arch, and at the top it is connected to the rest of the skull via the antorbital bridge. It is part of the maxillary bone, or upper jaw, which also contains the upper cheekteeth. Primitively, rodents have a nearly horizontal zygomatic plate. In association with specializations in zygomasseteric system, several distinct morphologies have developed across the order.

<i>Oryzomys albiventer</i> species of mammal

Oryzomys albiventer is a rodent in the genus Oryzomys of family Cricetidae from interior western Mexico, in the states of Jalisco, Guanajuato, and Michoacán. First described in 1901 as a separate species, it was later lumped under O. couesi and the marsh rice rat (O. palustris) until it was reinstated as a species in 2009. It differs from neighboring Oryzomys populations in size and measurements and is a large, brightly colored species with a long tail and robust skull and molars. Its range has been much impacted by agricultural development, but isolated populations are thought to persist.

The entepicondylar foramen is an opening in the distal (far) end of the humerus present in some mammals. It is often present in primitive placentals, such as the enigmatic Madagascan Plesiorycteropus. In most Neotominae and all Tylomyinae among cricetid rodents, it is located above the medial epicondyle of the humerus, but it is absent in all Sigmodontinae and Arvicolinae and this trait has been suggested as a synapomorphy for the former subfamily.

In mammals, ungual tufts are tufts of hairs at the base of claws of the fore- and hindfeet. Their presence has been used as a character in cladistic studies of Cricetidae.

Natatory fringes are rows of stiff hairs that occur along the margins of the hindfeet in some rodents. They occur along the plantar margins and in some cases also between the toes. Among sigmodontines, a mostly South American groups, natatory fringes are present in Ichthyomyini and some Oryzomyini. Among ichthyomyines, the fringes are poorly developed in Neusticomys but well-developed in other genera, and in Rheomys mexicanus the hairs of the fringes may exceed 3 millimetres (0.12 in) in length. Amphinectomys, Holochilus, Lundomys, and Nectomys are the only oryzomyines with natatory fringes, but have them only weakly developed; one study also records them in Oryzomys. In oryzomyines, the fringes are an adaptation for a semiaquatic lifestyle that appeared convergently in the Holochilus-Lundomys and Nectomys-Amphinectomys lineages. The term was introduced in 1993 by Voss and Carleton in describing Lundomys.

In rodents, the capsular process or projection is a bony capsule that contains the root of the lower incisor. It is visible on the labial (outer) side of the mandible as a raising in the bone. There is marked variation within species in the development of this process.

In rodents, incisor procumbency refers to the orientation of the upper incisor, defined by the position of the cutting edge of the incisor relative to the vertical plane of the incisors. Proodont incisors have the cutting edge in front of the vertical plane, orthodont teeth have it perpendicular to the plane, opisthodont incisors have it behind the plane, and hyper-opisthodont teeth have the cutting edge even behind the back of the alveolus of the incisor.

In some rodents, the subsquamosal fenestra is an opening between two parts of the squamosal bone, at the back of the skull. It can be seen in lateral view. Most Oryzomyini have the fenestra, but some species, including those in the genera Nectomys, Sigmodontomys, and Melanomys among others, lack it.

References

↑ Weksler, 2006, p. 37, fig. 20
1 2 3 Weksler, 2006, p. 37
↑ Weksler, 2006, p. 37; Steppan, 1995, pp. 37–38; Carleton, 1980, p. 44
1 2 Steppan, 1995, p. 38
↑ Moore, 1959, p. 179

Literature cited

Carleton, M.D. 1980. Phylogenetic relationships in neotomine-peromyscine rodents (Muroidea) and a reappraisal of the dichotomy within New World Cricetinae. Miscellaneous Publications, Museum of Zoology, University of Michigan 157:i–vii+1–146.
Moore, J.C. 1959. Relationships among the living squirrels of the Sciurinae. Bulletin of the American Museum of Natural History 118:157–206.
Steppan, S.J. 1995. Revision of the tribe Phyllotini (Rodentia: Sigmodontinae), with a phylogenetic hypothesis for the Sigmodontinae. Fieldiana Zoology 80:1–112.
Weksler, M. 2006. Phylogenetic relationships of oryzomyine rodents (Muroidea: Sigmodontinae): separate and combined analyses of morphological and molecular data. Bulletin of the American Museum of Natural History 296:1–149.

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[1] Weksler, 2006, p. 37, fig. 20

[W37-2] 1 2 3 Weksler, 2006, p. 37

[3] Weksler, 2006, p. 37; Steppan, 1995, pp. 37–38; Carleton, 1980, p. 44

[S38-4] 1 2 Steppan, 1995, p. 38

[M179-5] Moore, 1959, p. 179