Mammal Species of the World
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occurs (regularly, as a native taxon) in multiple nations
Regularity: Regularly occurring
Type of Residency: Year-round
Global Range: Eastern Texas to southeastern Kansas, east to southern New Jersey/Delaware and Florida (Honacki et al. 1982). Formerly recognized species O. ARGENTATUS, now included in O. PALUSTRIS, is known to occur on nine islands in the lower Florida Keys and probably occurs on several others (Goodyear 1987, 1992).
Length: 31 cm
Weight: 78 grams
Size in North America
Average: 226 mm males; 217 mm females
Range: 193-262 mm males; 191-253 mm females
Average: 56 g males; 48 g females
Range: 46-80 g males; 40-60 g females
Habitat and Ecology
Breeding may occur throughout the year, particularly early spring. Gestation lasts 21-28 days. Litter size is 4-6 (range 1-7). Several litters per year, up to six are known. Young are weaned within two weeks.
The average home range is one acre (Negus et al. 1961). This species is an effective disperser over water and a good colonizer of barrier islands (Loxterman et al. 1998). Diet includes rice and seeds of herbaceous plants. When available (in season), arthropods make up 75% of the diet (Negus et al. 1961). It is primarily nocturnal.
Comments: Prefers saltwater and freshwater marshes (semi-aquatic). May also be found in swamps and moist meadows. Uplands bordering wetlands may be important as refuges during high tides (Kruchek 2004). Able to move between adjacent islands by swimming across salt water; in Virginia, ten movements between two islands separated by 50 m and one movement between two islands separated by 300 m were documented (Forys and Dueser 1993, Forys and Moncrief 1994). Nests are placed in grassy vegetation under debris, or woven in aquatic emergents a foot or more above the high water line.
Non-Migrant: Yes. At least some populations of this species do not make significant seasonal migrations. Juvenile dispersal is not considered a migration.
Locally Migrant: No. No populations of this species make local extended movements (generally less than 200 km) at particular times of the year (e.g., to breeding or wintering grounds, to hibernation sites).
Locally Migrant: No. No populations of this species make annual migrations of over 200 km.
Comments: Prefers rice, seeds of herbaceous plants. When available (in season), arthropods make up 75% of diet (Negus et al. 1961).
Population densities range from less than 1 to 7 per acre in marginal, perhaps atypical sedge-shrub habitat (Negus et al. 1961). In Florida swamps, density was 20 per acre (Smith and Vrieze 1979).
Average home range is 1 acre (Negus et al. 1961, Birkenholz 1963).
This species is an effective disperser over water and a good colonizer of barrier islands (Loxterman et al. 1998).
Life History and Behavior
Comments: Primarily nocturnal.
Breeding may occur throughout the year, particularly early spring. At the northern end of the range in Delaware, breeding begins in late winter and extends into late summer (sometimes into fall) (Edmonds and Stetson 1993). Gestation lasts 21-28 days. Litter size is 4-6 (range 1-7). Several litters per year, up to 6 known. Young are weaned within 2 weeks.
IUCN Red List Assessment
Red List Category
Red List Criteria
National NatureServe Conservation Status
Rounded National Status Rank: N5 - Secure
NatureServe Conservation Status
Rounded Global Status Rank: G5 - Secure
Marsh rice rat
The marsh rice rat (Oryzomys palustris) is a semiaquatic North American rodent in the family Cricetidae. It usually occurs in wetland habitats, such as swamps and salt marshes. It is found mostly in the eastern and southern United States, from New Jersey and Kansas south to Florida and northeasternmost Tamaulipas, Mexico; its range previously extended further west and north, where it may have been a commensal in corn-cultivating communities. Weighing about 40 to 80 g (1.4 to 2.8 oz), the marsh rice rat is a medium-sized rodent that resembles the common black and brown rat. The upperparts are generally gray-brown, but are reddish in many Florida populations. The feet show several specializations for life in the water. The skull is large and flattened, and is short at the front.
John Bachman discovered the marsh rice rat in 1816, and it was formally described in 1837. Several subspecies have been described since the 1890s, mainly from Florida, but there is disagreement over their validity. The Florida Keys population is sometimes classified as a different species, the silver rice rat (Oryzomys argentatus). Data from the mitochondrial cytochrome b gene indicate a deep divergence between populations east of Mississippi and those further west, which suggests that the western populations may be recognized as a separate species, Oryzomys texensis. The species is part of the genus Oryzomys, which also includes several others occurring further south in Mexico, Central America, and northwestern South America, some of which have previously been regarded as subspecies of the marsh rice rat. One, Oryzomys couesi, occurs with the marsh rice rat in Tamaulipas and southern Texas.
The marsh rice rat is active during the night, makes nests of sedge and grass, and occasionally builds runways. It has a diverse diet that includes plants, fungi, and a variety of animals. Population densities are usually below 10 per ha (4 per acre) and home ranges vary from 0.23 to 0.37 ha (0.57 to 0.91 acres), depending on sex and geography. Litters of generally three to five young are born after a pregnancy of about 25 days, mainly during the summer. Newborns are helpless at birth, but are weaned after a few weeks. Several animals prey on the marsh rice rat, including the barn owl, and it usually lives for less than a year in the wild. It is infected by many different parasites and harbors a hantavirus that also infects humans. The species is not of conservation concern, but some populations are threatened.
- 1 Taxonomy
- 2 Description
- 3 Distribution and habitat
- 4 Behavior and ecology
- 5 Human interactions
- 6 References
- 7 Literature cited
The marsh rice rat is classified as one of eight species in the genus Oryzomys, which is distributed from the eastern United States (marsh rice rat) into northwestern South America (O. gorgasi). Oryzomys previously included many other species, which were reclassified in various studies culminating in contributions by Marcelo Weksler and coworkers in 2006 that removed more than forty species from the genus. All are placed in the tribe Oryzomyini ("rice rats"), a diverse assemblage of over a hundred species, and on higher taxonomic levels in the subfamily Sigmodontinae of the family Cricetidae, along with hundreds of other species of mainly small rodents, most of which occur in South and Central America. In the United States, the marsh rice rat is the only oryzomyine rodent except for Oryzomys couesi in a small area of southern Texas; the only other sigmodontines present are several species of cotton rats (Sigmodon) in the southern half of the country.
The marsh rice rat was discovered in 1816 in South Carolina by John Bachman. Bachman intended to describe the species as Arvicola oryzivora, but sent a specimen to Richard Harlan and Charles Pickering at the Academy of Natural Sciences in Philadelphia to confirm its identity. Another specimen, from New Jersey, was found in the Academy's collection, and Harlan took it upon himself, against Pickering's wishes, to describe the new species as Mus palustris, proclaiming it one of the few true rats of the United States. The specific name palustris is Latin for "marshy" and refers to the usual habitat of the species.
In 1854, in The quadrupeds of North America, Bachman redescribed it as Arvicola oryzivora, considering it more closely related to the voles then placed in the genus Arvicola, and also recorded it from Georgia and Florida. Three years later, Spencer Fullerton Baird argued that the referral of the species to Arvicola was erroneous and introduced a new generic name for the marsh rice rat, Oryzomys. The name combines the Greek oryza "rice" and mys "mouse" and refers to the rat's habit of eating rice. At the time, Oryzomys was recognized either as a full genus or as a subgenus of the now-defunct genus Hesperomys, but since the 1890s, it has been universally recognized as a genus distinct from Hesperomys, with the marsh rice rat (Oryzomys palustris) as its type species.
Species boundaries and subspecies
In the 1890s, several subspecies of the marsh rice rat were described from the United States: natator from Florida in 1893, texensis from Texas in 1894, and coloratus from elsewhere in Florida in 1898. Clinton Hart Merriam recognized natator as a separate species in 1901 and described a subspecies of it, floridanus, but considered texensis to be nearly identical to nominate palustris. In his 1918 revision of North American Oryzomys, Edward Alphonso Goldman again recognized all these as a single species, Oryzomys palustris. He distinguished four subspecies, which he said formed a "closely intergrading series"—O. p. palustris from New Jersey to southeastern Mississippi and eastern Missouri; O. p. natator in central Florida; O. p. coloratus (including O. natator floridanus Merriam) in southern Florida; and O. p. texensis from western Mississippi and southeastern Kansas to eastern Texas. Two additional subspecies were described by William J. Hamilton in 1955 from southern Florida: planirostris from Pine Island and two miles (3 km) north of Fort Myers and sanibeli from Sanibel Island. Also in 1955, Claude W. Hibbard described a new species of Oryzomys, O. fossilis, from Pleistocene deposits in Kansas, on the basis of small differences in characters of the tooth with living marsh rice rats. In 1965, Walter Dalquest demoted this species, later also found in Texas, to a subspecies, because it does not differ more from living marsh rice rats than the latter differ from each other.
Merriam and Goldman had recognized that a number of Central American species, including Oryzomys couesi and numerous forms with more limited distributions, are related to the marsh rice rat. O. couesi ranges north to southernmost Texas, where its distribution meets that of the marsh rice rat. In 1960, Raymond Hall argued that specimens from the contact zone were intermediate between the local forms of O. couesi and the marsh rice rat, and accordingly included the former in the marsh rice rat. While reporting on the ecology of Texan O. couesi in 1979, Benson and Gehlbach noted that populations of O. couesi and the marsh rice rat there were in fact distinct, with the latter being smaller and less brown and more gray in color; their karyotypes were also distinct. Since then, the two have generally been retained as distinct species, as supported by further research; a 1994 study even found the two to occur at some of the same places (in sympatry) in southern Texas and nearby Tamaulipas, Mexico.
In 1973, rice rats were discovered at Cudjoe Key in the Florida Keys, and in 1978 Spitzer and Lazell described this population as a new species, Oryzomys argentatus. The status of this form—either a distinct species or not even subspecifically distinct from O. palustris natator—has remained controversial since; the 2005 third edition of Mammal Species of the World does not recognize O. argentatus as a separate species, but acknowledges a need for further research. A 2005 study using microsatellite DNA found that Florida Keys rice rats exhibit low genetic variation and are significantly different from Everglades rice rats; the study concluded in favor of classifying the Keys rice rat as a "distinct vertebrate population". This population probably diverged from mainland rice rats about 2000 years ago.
Among the described subspecies, a 1989 morphometrical study by Humphrey and Setzer separated only two—natator from much of Florida (including coloratus, planirostris, sanibeli, and floridanus, as well as argentatus) and palustris from the rest of the range (including texensis). On the other hand, Whitaker and Hamilton in their 1998 book on the Mammals of the Eastern United States recognized planirostris and sanibeli as separate subspecies, but merged all others into O. palustris palustris, and placed O. argentatus as a separate species; their classification was based on their emphasis of overwater gaps as agents of biological diversification and a critique of shortcomings in Humphrey and Setzer's study, not on a reanalysis of the data.
In 2010, Delton Hanson and colleagues published a study of the relationships among populations of Oryzomys on the basis of data from three genes—the mitochondrial gene cytochrome b (Cytb) and two nuclear markers, exon 1 of the interphotoreceptor retinoid-binding protein gene (Rbp3) and intron 2 of alcohol dehydrogenase gene 1 (Adh1-I2). The Cytb data placed all marsh rice rats studied sister to a clade containing various populations of O. couesi; the mean genetic distance between the two groups was 11.30%. The marsh rice rats fell into two main groups, differing on average by 6.05%, one containing animals from Mississippi, southwestern Tennessee, and further west, and the other including specimens from Alabama and further east. Within the eastern group, variation was only about 0.65%, even though examples of the putative subspecies palustris, coloratus, sanibeli, and planirostris were all included. Data from both of the slower-evolving nuclear markers Rbp3 and Adh1-I2 also placed examples of Oryzomys in two main clades, but did not recover the western and eastern groups of the marsh rice rat as separate clades. In addition, Adh1-I2 placed a Costa Rican population within the marsh rice rat clade and some other southern Oryzomys specimens closer to the marsh rice rat than to the O. couesi group. The combined dataset supported the western and eastern clades within the marsh rice rat and placed the Costa Rican population marginally closer to the marsh rice rat than to O. couesi. Using the genetic species concept, the authors suggested that the western populations of the marsh rice rat be recognized as a separate species, Oryzomys texensis. They recommended further research in the Mississippi–Alabama–Tennessee region, where the ranges of the two meet.
Many common names have been proposed for the marsh rice rat. Early describers used "Rice Meadow-Mouse" and "Rice-field Mouse" and in the early 1900s, name such as "rice rat", "marsh mouse", and "swamp rice rat" came into use. Some of the subspecies received their own common names, such as "Florida Marsh Mouse", "Swimming Rice Rat", and "Central Florida Rice Rat" for O. p. natator; "Bangs' Marsh Mouse", "Cape Sable Rice Rat", and "Everglades Rice Rat" for O. p. coloratus; and "Texas Rice Rat" for O. p. texensis. The species is now usually known as the "marsh rice rat", although "marsh oryzomys" has also been in recent use. The Florida Keys form (argentatus) is known as the "silver rice rat".
|Population||n||Total length||Tail length||Hindfoot length|
|O. p. palustris (New Jersey)||4||242 (237–245)||112 (109–116)||31 (30–31.5)|
|O. p. natator (Florida)||10||281.2 (246–318)||140.6 (122–173)||33.1 (28–37)|
|O. p. coloratus (Florida)||11||283.0 (250–326)||143.5 (123–171)||33.4 (31–38)|
|O. p. texensis (Texas)||8||242 (226–279)||120 (108–133)||29 (28.5–30.5)|
|O. p. planirostris (Florida)||14||247.5 (226–266)||129.6 (108–128)||31 (29–33)|
|O. p. sanibeli (Florida)||11||257.5 (233–274)||123.6 (111–138)||31.0 (29–33)|
|O. argentatus (Florida Keys)||2||251, 259||121, 132||32, 32|
|Measurements are all in millimeters and are in the form "average (minimum–maximum)", except those of the Florida Keys population.|
n=Number of specimens measured.
The marsh rice rat is a medium-sized rodent that looks much like the common black and brown rats, but has greater differences in color between the upper- and underparts. The fur is thick and short. The upperparts are generally gray to grayish brown, with the head a bit lighter, and are sharply delimited from the underparts, which are off-white, as are the feet. There are small cheek pouches. The ears are about the same color as the upperparts, but there is a patch of light hairs in front of them. The tail is dark brown above and may be paler below. The guard hairs are long and have unpigmented, silvery tips. When rice rats swim, air is trapped in the fur, which increases buoyancy and reduces heat loss. As in most other oryzomyines, females have eight mammae.
The forefeet have four and the hindfeet five digits. On the forefeet, the ungual tufts (tufts of hair on the digits) are absent. The hindfeet are broad and have a short fifth digit. Many of the pads are reduced, as are the ungual tufts, but there are small interdigital webs. The Florida Keys form, argentatus, has even more reduced ungual tufts. Many of these traits are common adaptations to life in the water in oryzomyines.
There is some geographic variation in fur color: western populations (texensis) are lighter than those from the east (nominate palustris), and Florida populations are generally more tawny or reddish than either, with those from southern Florida (coloratus) being brighter than those from the center of the state (natator). The Florida Keys form (argentatus) is silvery, and the two other Florida forms—planirostris and sanibeli—lack the reddish tones of mainland Florida populations and are instead grayish, resembling nominate palustris (planirostris), or brownish (sanibeli). In 1989, Humphrey and Setzer reviewed variation in color among Florida populations. They found argentatus to be substantially lighter and planirostris and sanibeli to be somewhat darker than mainland populations, and argentatus to have a less yellow fur, but found no significant differences in redness. There was also substantial variation within populations.
Total length is 226 to 305 mm (8.9 to 12.0 in), tail length 108 to 156 mm (4.3 to 6.1 in), hindfoot length 28 to 37 mm (1.1 to 1.5 in), and body mass 40 to 80 g (1.4 to 2.8 oz), with males slightly larger than females. The largest individuals occur in Florida and along the Gulf Coast east of the Mississippi River delta.
The stomach has the characteristic pattern of sigmodontines (unilocular-hemiglandular): it is not split in two chambers by an incisura angularis and the front part (antrum) is covered by a glandular epithelium. The gall bladder is absent, a synapomorphy (shared-derived character) of Oryzomyini. The karyotype includes 56 chromosomes and a fundamental number of 60 chromosomal arms (2n = 56, FN = 60). The form of the sex chromosomes has been used to distinguish the marsh rice rat from Oryzomys couesi, but may be too variable among Oryzomys to be useful in differentiating species. X chromosome inactivation occurs in the marsh rice rat, even though the animal lacks LINE-1 retrotransposons, which have been suggested as components of the inactivation process. Mutants with fused or additional molars and with light fur have been recorded in laboratory colonies; the abnormal molars are apparently the result of a single autosomal recessive mutation. At about 50%, hematocrit (the proportion of red blood cells in the blood) is high in the marsh rice rat compared to other rodents; this may be an adaptation that enables the rice rat to increase oxygen capacity while swimming underwater.
Male reproductive anatomy
The glans penis is long and robust, averaging 7.3 mm (0.29 in) long and 4.6 mm (0.18 in) broad, and the baculum (penis bone) is 6.6 mm (0.26 in) long. As is characteristic of Sigmodontinae, the marsh rice rat has a complex penis, with the distal (far) end of the baculum ending in three digits. The central digit is notably larger than those at the sides. The outer surface of the penis is mostly covered by small spines, but there is a broad band of nonspinous tissue. The papilla (nipple-like projection) on the dorsal (upper) side of the penis is covered with small spines, a character the marsh rice rat shares only with Oligoryzomys and Oryzomys couesi among oryzomyines examined. On the urethral process, located in the crater at the end of the penis, a fleshy process (the subapical lobule) is present; it is absent in all other oryzomyines with studied penes except O. couesi and Holochilus brasiliensis. The baculum is deeper than it is wide.
Some features of the accessory glands in the male genital region vary among oryzomyines. In the marsh rice rat, a single pair of preputial glands is present at the penis. As is usual for sigmodontines, there are two pairs of ventral prostate glands and a single pair of anterior and dorsal prostate glands. Part of the end of the vesicular gland is irregularly folded, not smooth as in most oryzomyines.
The marsh rice rat has a large, flattened skull with a short and broad rostrum (front part). The nasal and premaxillary bones extend back beyond the point where the lacrimal, frontal, and maxillary bones meet. In planirostris, the rostrum is flatter than in mainland Florida forms, in which it is more convex, and the nasals are said to be relatively longer in argentatus. The zygomatic plate, the flattened front part of the zygomatic arch (cheekbone), is broad and develops a notch at its front end. The arches themselves are robust and contain small but distinct jugal bones. The sphenopalatine foramen, a foramen (opening) in the side of the skull above the molars, is large; it is much smaller in O. couesi. The narrowest part of the interorbital region (located between the eyes) is towards the front and the edges are lined by prominent shelves. The marsh rice rat has a narrow braincase lined by prominent ridges and a narrow interparietal bone. According to Goldman, Florida animals (coloratus and natator) generally have the largest and broadest skulls, and western specimens (texensis) have somewhat smaller and narrower skulls than those from the east outside Florida (nominate palustris). In argentatus, the skull is also relatively narrow.
The incisive foramina, openings in the front part of the palate, reach backward between the molars. The palate is long, extending substantially beyond the third molars. The back part, near the third molars, is usually perforated by prominent posterolateral palatal pits, which are recessed into fossae (depressions). The mesopterygoid fossa, the gap behind the end of the palate, is perforated by sphenopalatine vacuities, which are set far to the front. The condition of the arteries in the head is highly derived. The subsquamosal fenestra, an opening in the back part of the skull determined by the shape of the squamosal bone, is present. The squamosal lacks a suspensory process that contacts the tegmen tympani, the roof of the tympanic cavity, a defining character of oryzomyines. There are some openings in the mastoid bone.
In the mandible (lower jaw), the mental foramen, an opening just before the first molar, opens sidewards, not upwards as in a few other oryzomyines. The upper and lower masseteric ridges, which anchor some of the chewing muscles, join at a point below the first molar and do not extend forward beyond that point. The capsular process, a raising of the bone of the back of the mandible that houses the back end of the incisor, is present, but not as large as in O. couesi.
The dental formula is 220.127.116.11 × 2 = 16 (one upper and one lower incisor and three upper and three lower molars), as usual in muroid rodents. The upper incisors are well-developed and strongly opisthodont, with the chewing edge located behind the vertical plane of the teeth. The molars are bunodont, with the cusps higher than the connecting crests, and brachydont, low-crowned, as in most other oryzomyines. Many accessory crests, including the mesoloph on the upper molars and the mesolophid on the lower molars, are present, another trait the marsh rice rat shares with most but not all other oryzomyines. The flexi and flexids (valleys between the cusps and crests) at the labial (outer) side of the molars are closed by cingula (ridges).
The upper molars have two longitudinal rows of cusps, not three as in the black and brown rats. The first and second upper molar are oval in form and the flexi do not extend to the midline of the molars. The anterocone, the front cusp of the upper first molar, is not divided in two by an indentation at its front (anteromedian flexus), but does display a hollow in the middle, the anteromedian fossette, which divides it into separate cuspules at the labial and lingual (inner) sides of the molar. A crest, the anteroloph, is present behind the labial cuspule, but in older animals, the cusps and the crest are united into a single structure by wear. In the third upper molar, the cusps at the back are reduced and scarcely distinguishable. As in most oryzomyines, the upper molars all have one root on the inner (lingual) side and two on the outer (labial) side; in addition, the first upper molar usually has another small labial root.
The first lower molar is rounded at the front end and the labial and lingual conules of the anteroconid, the frontmost cusp, are barely distinct. The second lower molar is elongate and has a crest, the anterolophid, before the two cusps that form the front edge of the molar in some other oryzomyines, the protoconid and metaconid. There is a distinct ridge (anterolabial cingulum) at the outer front (anterolabial) edge of the molar, before the protoconid. The lower third molar is about as long as the second and also has an anterolophid, albeit a less well-defined one. The first lower molar has large roots at the front and back of the tooth and usually one or two smaller ones in between, at the labial and lingual side. The second and third lowers molars have either two roots, one labial and one lingual, or only one at the front, and another large root at the back.
As usual in oryzomyines, there are twelve ribs. The first rib articulates with both the last cervical (neck) and first thoracic (chest) vertebrae, a synapomorphy of the Sigmodontinae. Anapophyses, processes at the back of a vertebra, are absent from the fifth lumbar. Between the second and third caudal vertebrae, hemal arches (small bones) are present with a spinous back border. The entepicondylar foramen is absent, as in all members of the Sigmodontinae; if present, as in some other rodents, this foramen perforates the distal (far) end of the humerus (upper arm bone).
Studies have shown that in poor conditions the weight of the adrenal gland may increase up to 200%, that rice rats are unable to conserve water well when dehydrated, and that in water contaminated with oil they swim less and their mortality increases. The median amount of radiation needed to kill a marsh rice rat is 5.25 Gy and the lethal dose of potassium cyanide is 7.20 mg/kg; both values are relatively low for cricetid rodents. In one study, wild rice rats in radioactively contaminated areas did not show signs of disease. Experiments have found that exposure to more daylight and higher food availability cause increased development of the gonads in both adult and juvenile rice rats. When the pineal gland is removed or melatonin is administered in male rice rats, the testes are reduced and tend to regress into the body.
Distribution and habitat
The marsh rice rat currently occurs in much of the eastern and southern United States, northeast to southern New Jersey, and south to southeastern Texas and far northeastern Tamaulipas, Mexico. The northernmost records in the interior United States are in eastern Oklahoma, southeastern Kansas, southern Missouri and Illinois, and the southern half of Kentucky, but the species is absent in much of the Appalachians. Fossils of the marsh rice rat are known from Rancholabrean (late Pleistocene, less than 300,000 years ago) deposits in Florida and Georgia and remains referred to the extinct subspecies O. p. fossilis are from the Wisconsinan and Sangamonian of Texas and Illinoian and Sangamonian of Kansas. In the Florida Keys, rice rats occur on most of the Lower Keys, but are absent from the Upper Keys, which are of a different geological origin and were probably never connected to the mainland. The western and eastern Cytb clades within the marsh rice rat may represent expansions from different glacial refugia which the species was restricted to during a glacial period.
Cave and archeological remains indicate that the range of the marsh rice rat has extended substantially further north and west earlier in the Holocene, into central Texas, eastern Nebraska, southwestern Iowa, central Illinois, southern Indiana, southern Ohio, West Virginia, and southwestern Pennsylvania. Most northern archeological sites date from about 1000 CE and are associated with corn cultivation, but in some older cave sites the rice rat is found with the extinct giant armadillo Dasypus bellus, suggesting warm climatic conditions. Perhaps a warm period during the Quaternary enabled the rice rat to disperse northward and when the climate cooled, relict populations were able to survive in the north as commensals in corn-cultivating Native American communities. Some subfossil animals are slightly larger than living marsh rice rats, possibly because environmental constraints were relaxed in commensal populations.
In Tamaulipas and southern Texas, the ranges of the marsh rice rat and the related Oryzomys couesi meet; in parts of Kenedy, Willacy and Cameron counties, Texas, and in far northeastern Tamaulipas, the two are sympatric (occur in the same places). In experimental conditions, they fail to interbreed and genetic analysis yields no evidence of gene flow or hybridization in the wild. Compared to O. couesi, the marsh rice rat shows less genetic variability within but more between populations in the contact zone, probably because the species is restricted to isolated populations near the coast.
The marsh rice rat occurs in several habitats, ranging from coastal salt marshes to mountain streams and clearings. It is semiaquatic, spending much time in the water, and usually occurs in wetland habitats. It prefers areas where the ground is covered with grasses and sedges, which protect it from predators. In southern Illinois, marsh rice rats are more likely to occur in wetlands with more herbaceous cover, visual obstruction, and nearby grasslands. The species also occurs in drier uplands, which serve as sinks for young, dispersing animals and as refuges during high tide. Rice rats are adept overwater dispersers; studies on islands off Virginia's Delmarva Peninsula show that they readily cross 300-m (1000 ft) channels between islands.
Behavior and ecology
Marsh rice rats are active during the night and for this reason are rarely seen, although they may be among the most common small mammals in part of their range. They will build nests of sedge and grass, about 13 cm (5 in) large, which are placed under debris, near shrubs, in short burrows, or high in aquatic vegetation. They may also use old nests of marsh wrens (Cistothorus palustris), red-winged blackbirds (Agelaius phoeniceus), muskrats (Ondatra zibethicus) or round-tailed muskrats (Neofiber alleni). Marsh rice rats sometimes make large runways or dig burrows. They are accomplished and willing swimmers, easily swimming for more than 10 m (30 ft) under water, and will often seek safety in the water when alarmed. Rice rats in the Florida Keys occasionally climb in vegetation, but never higher than 90 cm (3 ft). Marsh rice rats are very clean and extensively groom themselves, perhaps to keep their fur water-repellent. They are aggressive towards conspecifics and emit high-pitched squeaks while fighting. In dense vegetation, the perceptual range (the distance from which an animal can detect a patch of suitable habitat) of marsh rice rats is less than 10 m (33 ft). When released outside of their natural wetland habitat, marsh rice rats generally move either upwind or downwind (anemotaxis), perhaps in order to move in a straight line, which is an efficient strategy to find suitable habitat.
Many animals prey on marsh rice rats. The barn owl (Tyto alba) is among the most important; one study found that 97.5% of vertebrate remains in barn owl pellets were marsh rice rats. Other predators include birds (marsh hawks, Circus cyaneus; and barred owls, Strix varia), snakes (cottonmouth moccasins, Agkistrodon piscivorus; and others), alligators, and carnivorans (raccoons, Procyon lotor; red foxes, Vulpes vulpes; minks, Neovison vison; weasels of the genus Mustela; and striped skunks, Mephitis mephitis). Many parasites have been recorded on the marsh rice rat, including various ticks and mites, lice, and fleas among external parasites and many nematodes and digeneans, a pentastomid, and several coccidians among internal parasites (see parasites of the marsh rice rat).
Periodontitis, a bacterial disease affecting the jaws, is particularly virulent in marsh rice rats; the animal has been proposed as a model for research on the disease in humans. The identity of the bacterial agent remains unknown. Vitamin E, fluoride, and iodide protect against bone loss associated with this disease in the rice rat and a high-sucrose diet increases the severity of periodontitis. A case of kyphosis has been observed in a North Carolina marsh rice rat.
The population density of the marsh rice rat usually does not reach 10 per ha (4 per acre). The weather may influence population dynamics; in the Everglades, densities may exceed 200 per ha (80 per acre) when flooding concentrates populations on small islands, In the Florida Keys, population density is less than 1 per ha (0.4 per acre). On Breton Island, Louisiana, perhaps an atypical habitat, home ranges in males average about 0.37 ha (0.81 acre) and in females about 0.23 ha (0.51 acre). A study in Florida found male home ranges to average 0.25 ha (0.56 acre) and female 0.33 ha (0.72 acre).
Population size is usually largest during the summer and declines during winter, although populations in Texas and Louisiana may be more seasonally stable. Animals also often lose weight during winter. Population size varies dramatically from year to year in southern Texas. In coastal Mississippi, a study found that storms probably do not cause the population to decline substantially and in Texas inundation of its habitat did not significantly influence population density. However, another study in Mississippi found that flooding did cause a marked decline in rice rat abundance.
In the northern part of its range, the species often occurs with the meadow vole (Microtus pennsylvanicus), but there is no evidence that they compete with each other. In the south, the hispid cotton rat (Sigmodon hispidus) and the rice rat regularly occur together; water levels are known to influence relative abundance of these two species in Florida. The cotton rat is mainly active during the day, which may help differentiate its niche from that of the rice rat.
The marsh rice rat takes both vegetable and animal food, and is more carnivorous than most small rodents are; dominant food items vary seasonally. Plants eaten include species of Spartina, Salicornia, Tripsacum, and Elymus, among others; it mainly eats seeds and succulent parts. A 2004 study found that it prefers Spartina alterniflora that have been fertilized with nitrogen and mainly eats the inner tissue of the stem, perhaps because nitrogen-fertilized plants contain much less dimethylsulfoniopropionate in their inner tissues. The marsh rice rat was a major pest on rice plantations, feeding on the rice when it was newly planted. It also eats the fungus Endogone at times.
Animals that are important to the marsh rice rat's diet include insects, fiddler crabs, and snails, but the species is known to eat many other animals, including fish, clams, and juvenile Graptemys and Chrysemys turtles. They scavenge on carcasses of muskrats, deermice, and sparrows, and may be the most important predator on eggs and young of the marsh wren. Rice rats also eat eggs and young of the seaside sparrow (Ammodramus maritimus) and are aggressive towards the sparrow, apparently leading it to avoid nesting in Juncus in a seaside salt marsh in Florida. On islands in North Carolina, rice rats consume eggs of Forster's tern (Sterna forsteri). They have been observed preying on alligator eggs in Georgia.
Laboratory studies have found that rice rats assimilate 88% to 95% of the energy in their food. They lose weight when fed on Spartina, fiddler crabs, or sunflower seeds alone, but a diet consisting of several of those items or of mealworms is adequate to maintain weight. In an experiment, marsh rice rats did not show hoarding behavior, but wild rice rats have been observed carrying food to a nest. Even when they live in uplands, they mostly eat water plants and animals, although they consume some upland plants.
Reproduction and life cycle
Breeding occurs mostly during the summer. Some studies report that breeding ceases entirely during the winter, but winter breeding occurs as far north as Virginia. This is primarily because photoperiod influences their circadian rhythm which determines breeding. In both Texas and Virginia, there is less variation in reproductive activity in females than in males. In the south of its range, animals may breed less when the summer is at its warmest. The duration of the estrous cycle ranges from 6 to 9 days, with an average of 7.72 days. Estrus occurs again after a litter is born. A 1970 study reported that copulatory behavior in the marsh rice rat is similar to that in laboratory brown rats. Before mating starts, "the male pursues the running female from behind." The male then repeatedly mounts and dismounts the female; not all mounts result in an ejaculation. Penetrations only last for about 250 ms, but during mating the penetrations and the intervals between them become longer. Even when a male is satiated after mating, it is able to copulate again when a new female is introduced (the Coolidge effect). Partly because of resistance by the female, the frequency of ejaculation during mating is rather low in marsh rice rats as compared to laboratory rats, hamsters, and deermice.
|Age (days)||Body mass (g)||Body mass (oz)|
After a gestation of about 25 days, three to five young are usually born, although litter sizes vary from one to seven. Females may have up to six litters a year. Newborns weigh 3 to 4 g (about 0.1 to 0.15 oz) and are blind and almost naked. About as many males as females are born. The external ears (pinnae) soon unfold and on the first day claws are visible and the young emit high-pitched squeaks. On the second day, they are able to crawl and during the third to fifth days the whiskers and eyelids develop. On the two subsequent days, the mammae and incisors become visible and the animals become more active. Between the eighth and eleventh day, the eyes open, the fur develops, and the young begin to take solid food. Weaning occurs on the eleventh to twentieth day according to different studies. There is considerable variation in reported body masses at different ages, perhaps because of geographic variation. Sexual activity commences when the animals are about 50 to 60 days old. In the wild, rice rats usually live for less than a year; one study suggested that the average lifespan is only seven months.
The marsh rice rat is generally of little importance to humans, which is perhaps why it is not as well-studied as some other North American rodents. In 1931, Arthur Svihla noted that virtually no information had been published on the habits and life history of the marsh rice rat since the 1854 publication of Audubon and Bachman's description. Writing on Everglades mammals, Thomas E. Lodge notes that although the name "rat" may associate it unpleasantly with the introduced black and brown rats, its appearance is more endearing, even cute. J.S. Steward proposed the marsh rice rat as a model organism in 1951 to study certain infections that other rodents used at the time are not susceptible to. The marsh rice rat is quite susceptible to periodontitis and has been used as a model system for the study of that disease.
The marsh rice rat is the primary host of the Bayou virus (BAYV), the second most common agent of hantavirus infections in the United States. About 16% of animals are infected and the virus is most prevalent in old, heavy males. The virus may be transmitted among rice rats through bites inflicted during fights. It is also present in rice rat saliva and urine and human infections may occur because of contact with these excreta. Two related hantaviruses, Catacama virus and Playa de Oro virus, are known from Oryzomys couesi in Honduras and western Mexico, respectively. An arenavirus normally associated with woodrats (Neotoma) has also been found in Florida marsh rice rats. Antibodies against Borrelia burgdorferi, the bacterium that causes Lyme disease in the United States, have been found in marsh rice rats in Virginia, Maryland, North Carolina, and Tennessee. Another pathogenic bacterium, Bartonella, is known from Georgia marsh rice rats.
The 2009 IUCN Red List assesses the conservation status of the marsh rice rat as "Least Concern", because it is a common, widespread, and stable species without major threats that occurs in several protected areas. The Florida Keys form is rare and in decline and is threatened by competition with the black rat, predation by domestic cats, habitat loss, and loss of genetic variation; it is considered endangered. At the northern edge of its distribution, the marsh rice rat is listed as threatened in Illinois and whether it persists in Pennsylvania is unclear; it probably formerly occurred in tidal marshes on the Delaware River. In Illinois, its population may have regenerated because wetlands have been developed to protect waterfowl and shorebirds and because suitable wetlands often develop in abandoned coal-mining operations. A 2001 study projected that climate change would reduce the range of the marsh rice rat in Texas, where it is now common but may become threatened by habitat loss in the future. A study at the Paducah Gaseous Diffusion Plant found that rice rats accumulate more PCBs but less heavy metal than white-footed mice (Peromyscus leucopus).
- Linzey and Hammerson, 2008
- Harlan, 1837, p. 385
- Audubon and Bachman, 1854, p. 214
- Baird, 1857, p. 459
- Chapman, 1893, p. 44
- Allen, 1894, p. 177
- Bangs, 1898, p. 189
- Merriam, 1901, p. 277
- Hibbard, 1955, p. 213
- Hamilton, 1955, p. 83
- Hamilton, 1955, p. 85
- Spitzer and Lazell, 1978, p. 787
- Musser and Carleton, 2005, p. 1152; Miller and Kellogg, 1955, p. 430
- Carleton and Arroyo-Cabrales, 2009, p. 106
- Weksler et al., 2006, table 1
- Weksler, 2006, p. 3
- Musser and Carleton, 2005
- Chapman, 1893, p. 43
- Audubon and Bachman, 1854, p. 216
- Audubon and Bachman, 1854, p. 216; Harlan, 1837, p. 386; Chapman, 1893, p. 43; Goldman, 1918, pp. 8–9
- Merritt, 1987, p. 173; Schwartz and Schwartz, 2001, p. 192
- Baird, 1857, pp. 458, 482, 484; Goldman, 1918, p. 9
- Goldman, 1918, p. 9; Carleton and Arroyo-Cabrales, 2009, p. 116
- Merriam, 1901, pp. 276–277
- Goldman, 1918, p. 22
- Dalquest, 1965, p. 70
- Merriam, 1901, p. 275; Goldman, 1918, p. 20
- Hall, 1960, pp. 172–173
- Benson and Gehlbach, 1979, p. 227, table 2
- Schmidt and Engstrom, 1994, p. 419; Musser and Carleton, 2005, p. 1147
- Goodyear, 1991, p. 423
- Humphrey and Setzer, 1989, p. 557
- Musser and Carleton, 2005, p. 1153
- Wang et al., 2005, p. 575
- Wang et al., 2005, p. 581
- Humphrey and Setzer, 1989, p. 557; Musser and Carleton, 2005, p. 1152
- Whitaker and Hamilton, 1998, p. 281; Musser and Carleton, 2005, p. 1152
- Hanson et al., 2010, p. 337
- Hanson et al., 2010, figs. 1–2, table 1
- Hanson et al., 2010, figs. 1, 3–4
- Hanson et al., 2010, fig. 5
- Hanson et al., 2010, p. 342
- Baird, 1857, p. 482
- Stone and Cram, 1903, p. 129; Eliot, 1905, p. 275; Steward, 1951, p. 427
- Stone and Cram, 1903, p. 130
- Eliot, 1905, p. 181
- Goldman, 1918, p. 25
- Goldman, 1918, p. 26
- Goldman, 1918, p. 27
- Wolfe, 1982, p. 1; Linzey and Hammerson, 2008; Whitaker and Hamilton, 1998, p. 278
- Musser and Carleton, 2005, p. 1152; Milazzo et al., 2006, p. 1003
- Goldman, 1918, p. 23
- Hamilton, 1955, table 1
- Wolfe, 1982, p. 1; Whitaker and Hamilton, 1982, pp. 278–279; Kays and Wilson, 2000, p. 108
- Carleton and Musser, 1989, pp. 22–23
- Whitaker and Hamilton, 1982, p. 279; Kays and Wilson, 2000, p. 108; Goldman, 1918, p. 23; Carleton and Musser, 1989, p. 24; Merritt, 1987, p. 173
- Carleton and Musser, 1989, p. 23
- Esher et al., 1978, p. 551
- Wolfe, 1982, p. 1
- Weksler, 2006, p. 23
- Carleton and Musser, 1989, p. 24; Weksler, 2006, pp. 23–25
- Spitzer and Lazell, 1978, p. 787; Whitaker and Hamilton, 1998, p. 276
- Weksler, 2006, pp. 79, 81
- Goldman, 1918, p. 20
- Whitaker and Hamilton, 1998, p. 279; Wolfe, 1982, p. 1; Goldman, 1918, p. 20
- Kays and Wilson, 2000, p. 108
- Humphrey and Setzer, 1989, p. 558
- Humphrey and Setzer, 1989, pp. 563–564
- Weksler, 2006, p. 59
- Weksler, 2006, pp. 58–59
- Whitaker and Hamilton, 1998, p. 279
- Hershkovitz, 1987, p. 154
- Cantrell et al., 2009, p. 1
- Wolfe, 1982, p. 4
- Sofaer and Shaw, 1971, p. 99
- Stalling and Haynes, 1982, p. 301
- Stalling and Haynes, 1982, p. 306
- Goldman, 1918, plate I, figs. 1, 1a, 2, 2a
- Goldman, 1918, plate V, fig. 1
- Hooper and Musser, 1964, p. 13
- Hooper and Musser, 1964, table 1
- Weksler, 2006, pp. 55–56
- Weksler, 2006, pp. 56–57
- Hooper and Musser, 1964, p. 13; Weksler, 2006, p. 57
- Hooper and Musser, 1964, p. 7
- Weksler, 2006, p. 57
- Weksler, 2006, pp. 57–58; Voss and Linzey, 1981, p. 13
- Carleton and Musser, 1989, p. 25
- Weksler, 2006, pp. 27–28, table 5
- Spitzer and Lazell, 1978, p. 788
- Carleton and Musser, 1989, p. 26
- Schmidt and Engstrom, 1994, p. 917
- Carleton and Musser, 1989, p. 27; Weksler, 2006, p. 28, table 5
- Carleton and Musser, 1989, p. 29
- Goldman, 1918, pp. 23–27
- Carleton and Musser, 1989, p. 30
- Weksler, 2006, p. 37
- Weksler, 2006, pp. 38–39
- Weksler, 2006, p. 40
- Weksler, 2006, pp. 40–41
- Weksler, 2006, p. 41, table 5
- Weksler, 2006, p. 42
- Weksler, 2006, pp. 41–42
- Carleton and Musser, 1984, p. 292
- Carleton and Musser, 1989, p. 37
- Weksler, 2006, pp. 43–44
- Weksler, 2006, pp. 44–49
- Weksler, 2006, p. 44
- Whitaker and Hamilton, 1998, pp. 278–279
- Carleton and Musser, 1989, pp. 40, 42
- Carleton and Musser, 1989, pp. 39–40
- Carleton and Musser, 1989, p. 42
- Carleton and Musser, 1989, pp. 45–46; fig. 26A
- Goldman, 1918, plate VI, figs. 1, 1a
- Carleton and Musser, 1989, p. 43
- Weksler, 2006, p. 49
- Carleton and Musser, 1989, p. 44
- Carleton and Musser, 1989, p. 46, fig. 27A, B
- Weksler, 2006, p. 52, table 5
- Weksler, 2006, pp. 52–53
- Weksler, 2006, p. 53; fig. 28
- Weksler, 2006, p. 54
- Wolfe, 1982, p. 2
- Wolfe and Esher, 1981, p. 489
- O'Farrell and Dilley, 1975, table 1
- Childs and Cosgrove, 1966, p. 309
- Edmonds et al., 2003, p. 41
- Edmonds and Stetson, 1995, p. 274
- Musser and Carleton, 2005, p. 1152; Wolfe, 1982, p. 1; Schmidt and Engstrom, 1994, p. 914
- Wolfe, 1982, p. 1; Musser and Carleton, 2005, p. 1142
- Weksler, 2006, p. 88; Wolfe, 1982, p. 1
- Wolfe, 1982, p. 1; Hibbard, 1955, p. 213; Dalquest, 1962, p. 575; 1965, pp. 63, 70
- Whitaker and Hamilton, 1998, p. 277
- Wolfe, 1982, p. 1; Musser and Carleton, 2005, p. 1142; Richards, 1980, fig. 1; Winkler, 1990, p. 202
- Richards, 1980, pp. 429–430
- Richards, 1980, pp. 426, 429
- Schmidt and Engstrom, 1994, p. 914
- Schmidt and Engstrom, 1994, p. 916
- Schmidt and Engstrom, 1994, pp. 915–916
- Schmidt and Engstrom, 1994, p. 920
- Schmidt and Engstrom, 1994, p. 922
- Wolfe, 1982, p. 2; Whitaker and Hamilton, 1998, p. 279
- Eubanks et al., 2011, p. 552
- Kruchek, 2004, p. 569
- Forys and Duesser, 1993, p. 411
- Whitaker and Hamilton, 1998, p. 279; Wolfe, 1982, p. 4; Nesmith and Cox, 1985
- Whitaker and Hamilton, 1998, p. 279; Wolfe, 1982, p. 3; Esher et al., 1978, p. 556
- Schmidly and Davis, 2004, p. 381
- Goodyear, 1992, p. 190
- Whitaker and Hamilton, 1998, p. 279; Wolfe, 1982, pp. 3–4
- Schooley and Branch, 2005, pp. 59, 63
- Schooley and Branch, 2005, pp. 64–65
- Whitaker and Hamilton, 1998, p. 281; Wolfe, 1982, pp. 2–3
- Whitaker and Hamilton, 1998, p. 281; Wolfe, 1982, p. 4; Durden and Kollars, 1997
- Leopard, 1979, pp. 643–645
- Cohen and Meyer, 1993, p. 601; Shklair and Ralls, 1988, p. 25; Beiraghi et al., 1988, p. 99
- Webster, 1987, p. 172
- Whitaker and Hamilton, 1998, p. 281
- Bloch and Rose, 2005, p. 302
- Wang et al., 2005, p. 576
- Wolfe, 1982, pp. 2–3
- Wolfe, 1982, p. 2; Kruchek, 2004, p. 573
- Wolfe, 1982, pp. 1–2
- Abuzeineh et al., 2007, p. 75
- Chamberlain and Leopold, 2003, p. 307
- Wolfe, 1982, p. 3
- Otto et al., 2004, p. 1922
- Reid, 2006, p. 303
- Whitaker and Hamilton, 1998, p. 280; Wolfe, 1982, p. 3
- Whitaker and Hamilton, 1998, pp. 279–280; Wolfe, 1982, p. 3
- Post, 1981, p. 35
- Post, 1981, p. 40
- Brunjes and Webster, 2003, p. 654
- Hunt and Ogden, 1991, p. 450
- Whitaker and Hamilton, 1998, p. 280; Edmonds et al., 2003, p. 41; Bloch and Rose, 2005, p. 303; Negus et al., 1961, p. 103
- Dewsbury, 1970, p. 268
- Dewsbury, 1970, p. 269
- Dewsbury, 1970, p. 271
- Dewsbury, 1970, p. 274
- Whitaker and Hamilton, 1998, p. 280; Wolfe, 1982, p. 2; Linzey and Hammerson, 2008
- Negus et al., 1961, p. 103
- Svihla, 1931, p. 238
- Lodge, 2005, p. 177
- Steward, 1951, p. 429
- Oz and Puleo, 2011, pp. 2–3
- McIntyre et al., 2005, p. 1043
- McIntyre et al., 2005, p. 1048
- Milazzo et al., 2006, p. 1003; Chu et al., 2008, p. 188
- Kosoy et al., 1996, p. 574
- Oliver et al., 1999, p. 578; Kollars et al., 1996, p. 130
- Kosoy et al., 1997, table 2
- Whitaker and Hamilton, 1998, p. 278; Kays and Wilson, 2000, p. 108; Wang et al., 2005, pp. 575–576, 581
- Hofmann et al., 1990, p. 162; Eubanks et al., 2011, p. 558
- Merritt, 1987, p. 176
- Eubanks et al., 2011, pp. 558–559
- Cameron and Scheel, 2001, table 3, pp. 668–669
- Schmidly and Davis, 2004, p. 382
- Smith et al., 2002, p. 261
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Names and Taxonomy
Comments: Analysis of cranial variation in Oryzomys by Humphrey and Setzer (1989) indicated that O. argentatus should be included in this species. Only two subspecies were recognized by Humphrey and Setzer (1989): O. p. palustris (includes former subspecies palustris and texensis) and O. p. natator (includes former subspecies natator , coloratus, planirostris, and sanibeli, and former species O. argentatus). Goodyear (1991) reinstated O. argentatus as a species, but this was not followed by Baker et al. (2003), and Musser and Carleton (in Wilson and Reeder (1993, 2005) cited the more thorough study by Humphrey and Setzer (1979) in not accepting argentatus as a species (though they did state that the status of argentatus merits further study using genetic techniques).
Oryzomys palustris and O. couesi formerly were considered to be conspecific (Hall 1981); they were regarded as separate species by Honacki et al. (1982), Jones et al. (1986, 1992), and Musser and Carleton (in Wilson and Reeder 1993, 2005), following Benson and Gehlbach (1979). An electrophoretic study by Schmidt and Engstrom (1994) also concluded that O. palustris and O. couesi are distinct species. The taxonomic scope of the genus Oryzomys is unsettled, as are the taxonomic limits of some of the species included in the genus Oryzomys (Musser and Carleton, in Wilson and Reeder 1993, 2005).