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Oryzomys is a genus of semiaquatic rodents in the tribe Oryzomyini living in southern North America and far northern South America. It includes eight species, two of which—the marsh rice rat ( O. palustris) of the United States and Oryzomys couesi of Mexico and Central America—are widespread; the six others have more restricted distributions. The species have had eventful taxonomic histories, and most species were at one time included in the marsh rice rat; additional species may be recognized in the future. The name Oryzomys was established in 1857 by Spencer Fullerton Baird for the marsh rice rat and was soon applied to over a hundred species of American rodents. Subsequently, the genus gradually became more narrowly defined until its current contents were established in 2006, when ten new genera were established for species previously placed in Oryzomys.
Species of Oryzomys are medium-sized rats with long, coarse fur. The upperparts are gray to reddish and the underparts white to buff. The animals have broad feet with reduced or absent ungual tufts of hair around the claws and, in at least some species, with webbing between the toes. The rostrum (front part of the skull) is broad and the braincase is high. Both the marsh rice rat and O. couesi have 56 , lack a gall bladder, and have a complex penis (as is characteristic of the Sigmodontinae) with some traits that are rare among oryzomyines; these characteristics are unknown in the other species of this genus.
The habitat includes various kinds of wetlands, such as lakes, marshes, and rivers. Oryzomys species swim well, are active during the night, and eat both plant and animal food. They build woven nests of vegetation. After a gestation period of 21 to 28 days, about four young are born. Species of Oryzomys are infected by numerous and carry at least three , one of which (Bayou virus) also infects humans. Two, maybe three, species have gone extinct over the last two centuries and at least one other is endangered, but the widespread marsh rice rat and O. couesi are not threatened.
Within Oryzomyini, a 2006 phylogenetics analysis by Marcelo Weksler which used both morphological and DNA sequence data found some evidence that Oryzomys is most closely related to a group including Holochilus, Lundomys, and Pseudoryzomys. Although analyses based on morphological and combined data supported this relationship, sequences of the Rbp3 gene alone instead placed Oryzomys among a group that included Nectomys, Sigmodontomys, and a few other genera. In all analyses, Oryzomys appeared within clade D of Oryzomyini.Weksler, 2006, figs. 34–39 The relationship between Oryzomys and the Holochilus group was supported by five synapomorphy (shared derived characters)—absence or reduction of both the hypothenar and interdigital pads; reduction of of hairs surrounding the claws; having the back margin of the zygomatic plate of the skull at the same level as the front of the first upper molar; and the anterocone (front cusp) of the first upper molar divided by an anteromedian fossette. The first three are adaptations to the semiaquatic lifestyle that Oryzomys and the members of the Holochilus group share, and may thus be examples of convergent evolution.
Hershkovitz and Ray's classification was never widely followed, and from 1976 on authors started to reinstate some of the other groups lumped in Oryzomys as separate genera.Weksler, 2006, p. 10, table 1; Musser and Carleton, 2005, p. 1144 The genus was reduced to 43 species (out of 110 in Oryzomyini) in the third edition (2005) of Mammal Species of the World,Musser and Carleton, 2005, p. 900 but it was still not a natural, monophyly group;Musser and Carleton, 2005, p. 1144; Weksler, 2006, p. 10 rather, it mostly united those oryzomyines that lacked the conspicuous specializations of other genera.Weksler, 2006, p. 82 In 2006, Marcelo Weksler's comprehensive phylogenetic analysis produced further evidence that the genus was polyphyly, as species of Oryzomys were dispersed all over the oryzomyine tree. He proposed that eleven new genera should be created to accommodate those species that were not closely related to the type species of Oryzomys, the marsh rice rat;Weksler, 2006, p. 75 he considered other options that would require fewer new genera, but argued that that would result in less meaningful genus-level groups in Oryzomyini.Weksler, 2006, fig. 42, p. 77 Later in the same year, Weksler, Percequillo, and Voss created ten new genera— Aegialomys, Cerradomys, Eremoryzomys, Euryoryzomys, Hylaeamys, Mindomys, Nephelomys, Oreoryzomys, Sooretamys, and Transandinomys—for species formerly placed in Oryzomys and placed six more species related to "Oryzomys" alfaroi in Handleyomys pending the description of more new genera for them.Weksler et al., 2006, pp. 1–2 They left only five species in Oryzomys, which was now finally a natural, monophyletic group. Because of subsequent taxonomic work, the number of species has since increased to at least eight.Carleton and Arroyo-Cabrales, 2009, pp. 115–116; Weksler et al., 2006, table 1
Some problems remain: ? Oryzomys pliocaenicus, a Miocene fossil from Kansas, is of uncertain identity but may belong in Bensonomys,Weksler, 2006, p. 87 and fossils from the Miocene of Oregon and Pliocene of New Mexico have also been ascribed to Oryzomys, but probably incorrectly. A possible Oryzomys has been recorded from the Irvingtonian (Pleistocene) of Saskatchewan.Churcher, 1984, p. 149
In 2006, Weksler and colleagues followed the 2001 definition by Sánchez and others for the restricted genus Oryzomys, but added O. antillarum from Jamaica as a species.Weksler, 2006, table 1, footnote e Carleton and Joaquin Arroyo-Cabrales reviewed Oryzomys from western Mexico in 2009 and in this context provided an extended diagnosis of Oryzomys. They recognized eight species: the six previously mentioned plus O. albiventer and O. peninsulae. Also in 2009, Robert Voss and Weksler identified the subfossil Oryzomys curasoae from Curaçao as an island population of O. gorgasi.Voss and Weksler, 2009, p. 73 The next year, Delton Hanson and colleagues published a study using DNA sequence data from the cytochrome b, interphotoreceptor retinoid-binding protein, and alcohol dehydrogenase 1 genes to assess relationships within Oryzomys. They recommended that the marsh rice rat be split into two species and that O. couesi be split into four species on the basis of the observed sequence divergence and other data.
Merriam divided his palustris-mexicanus group in two "series" according to the color of the underparts (white or ).Merriam, 1901, p. 275 Goldman divided his palustris group in two "sections"—a couesi section with O. couesi and six related species, and a palustris section with O. palustris only. He noted that the latter differed from the former in the generally darker, more brownish, longer fur, and larger sphenopalatine vacuities (openings in the mesopterygoid fossa, the gap behind the end of the palate).Goldman, 1918, p. 20 As Weksler's 2006 analysis included only O. couesi and the marsh rice rat among species of Oryzomys in the strict sense, he could not test those groups.Weksler, 2006, table 4 Carleton and Arroyo-Cabrales concurred with Goldman's division, listing additional characters, and noted that the palustris group may be more semiaquatically adapted than the members of the couesi group are. In the latter, the fur is usually reddish-brown, as opposed to grayish-brown in the palustris group. Members of the couesi group have smaller sphenopalatine vacuities and a smaller sphenopalatine foramen, a foramen (opening) in the side of the skull above the molars, and a more highly developed anterolabial cingulum on the third lower molar (a crest at the front of the tooth). The hypothenar pad of the hindfoot, located on the sole far from the fingers, is present in the couesi group, but absent in the palustris group. Interdigital webbing may be more highly developed in the palustris group.Carleton and Arroyo-Cabrales, 2009 Using morphological data, Voss and Weksler found a closer relationship between O. couesi and O. gorgasi to the exclusion of O. palustris, but with low confidence.Voss and Weksler, 2009, fig. 1 The DNA sequence data of Hanson and colleagues supported a deep separation between the palustris and couesi groups, but a Costa Rican sample (assigned to O. couesi) was about as distant from the two groups as they were from each other.Hanson et al., 2010, figs. 2–5, table 1
The genus currently includes the following species:
The karyotype has been recorded in various populations of the marsh rice rat and O. couesi and is apparently stable within the genus at 56 , with the fundamental number of chromosomal arms ranging from 56 to 60 (2n = 56, FN = 56–60). In both species, the stomach has the characteristic pattern of sigmodontines (Locule-hemiglandular): it is not split in two chambers by an incisura angularis and the front part (antrum) is covered by a glandular epithelium.Weksler, 2006, p. 59 Furthermore, the gall bladder is absent, a synapomorphy of Oryzomyini.Weksler, 2006, pp. 58–59
Oryzomys species have a large skull with a short rostrum and high braincase. The interorbital region, located between the eyes, is narrowest to the front and is flanked by well-developed beads at its margins. The zygomatic plate is broad and has a well-developed zygomatic notch at its front. The zygomatic arch is robust and contains a small but distinct jugal bone. The interparietal bone, part of the roof of the braincase, is narrow and short;Goldman, 1918, p. 19; Carleton and Arroyo-Cabrales, 2009, p. 116 its narrowness is a synapomorphy for O. couesi plus the marsh rice rat according to Weksler's analysis.Weksler, 2006, p. 131 The incisive foramina are long, with their back margin at the front of the first molars or further back. The palate is also long, extending beyond the back margin of the bone, and is perforated near the third molars by well-developed posterolateral palatal pits. There is no alisphenoid strut, an extension of the alisphenoid bone that in some other oryzomyines separates two foramina in the skull. The are large. The condition of the artery in the head is highly Synapomorphy. In the mandible (lower jaw), the coronoid process, a process at the back, is well developedGoldman, 1918, p. 19 and the capsular process, a raising of the mandibular bone housing the root of the lower incisor, is conspicuous.
As usual in oryzomyines, the molars are pentalophodont (have the and , accessory crests, well developed) and bunodont, with the cusps higher than the connecting crests. The cusps on the upper molars are arranged in two longitudinal series, not three as in the black and brown rats.Wolfe, 1982, p. 1; Whitaker and Hamilton, 1998, pp. 278–279 The front cusps of the first upper and lower molar (anterocone and anteroconid, respectively) are broad and not divided completely by an anteromedian flexus or flexid. Behind the anterocone, the anteroloph (a smaller crest) is complete and separated from the anterocone. On both the second and third lower molars, the anterolophid (a crest on the inner front corner) is present, a putative synapomorphy of the genus. The first molars have additional small roots in addition to the main ones, so that the upper first molar has four and the lower has three or four roots.
As is characteristic of Sigmodontinae, the marsh rice rat and O. couesi have a complex penis, with the baculum (penis bone) displaying large protuberances at the sides.Weksler, 2006, pp. 55–56 The outer surface of the penis is mostly penile spines, but there is a broad band of nonspinous tissue.Weksler, 2006, pp. 56–57 The papilla (nipple-like projection) on the dorsal (upper) side of the penis is covered with small spines, a character these two species share only with Oligoryzomys among oryzomyines examined.Hooper and Musser, 1964, p. 13; Weksler, 2006, p. 57 On the urethral process, located in the crater at the end of the penis,Hooper and Musser, 1964, p. 7 a fleshy process (the subapical lobule) is present; it is absent in all other oryzomyines with studied penes except Holochilus brasiliensis.Weksler, 2006, p. 57 Both traits are recovered as synapomorphies of O. couesi plus the marsh rice rat in Weksler's analysis.
Behavior is known mainly from the marsh rice rat and O. couesi, with some scattered data from the other species. Oryzomys are semiaquatic, spending much time in the water, and otherwise mainly live on the ground;Reid, 2009, p. 205 both the marsh rice rat and O. couesi are known to be excellent swimmers and will flee into the water when disturbed.Esher et al., 1978, p. 556; Cook et al., 2001; Whitaker and Hamilton, 1998, p. 279; Reid, 2009, p. 279 Both are also nocturnal and build nests of interwoven vegetation, which may be suspended above the water.Reid, 2009, p. 207; Whitaker and Hamilton, 1998, p. 279; Wolfe, 1982, p. 4; Hall and Dalquest, 1963, p. 289 Breeding may occur throughout the year in both species, but is known to be seasonally variable in the marsh rice rat.Bloch and Rose, 2005, p. 303; Medellín and Medellín, 2006, p. 710 In both, gestation takes about 21 to 28 days and litter size is usually one to seven, averaging three to five.Jones and Engstrom, 1986, p. 12; Medellín and Medellín, 2006, p. 710; Reid, 2009, p. 207; Whitaker and Hamilton, 1998, p. 280; Wolfe, 1982, p. 2; Linzey and Hammerson, 2008 Young marsh rice rats and O. couesi become reproductively active when about 50 days old.Medellín and Medellín, 2006, p. 710; Wolfe, 1982, p. 2
The marsh rice rat, O. couesi, and O. gorgasi are known to be , eating both plant and animal material. They eat both seeds and green plant parts and consume a variety of animals, including , , and many others.Medellín and Medellín, 2006, p. 710; Reid, 2006, p. 207; Sánchez et al., 2001, p. 211; Whitaker and Hamilton, 1998, p. 280 The barn owl ( Tyto alba) is a major predator on the marsh rice ratWolfe, 1982, p. 2 and remains of O. antillarum, O. couesi, and O. gorgasi have been found in owl pellet deposits.Anthony, 1920, p. 166; Woodman, 1995, p. 1, table 1; McFarlane and Debrot, 2001, p. 182 Several other animals are known to prey on Oryzomys.Whitaker and Hamilton, 1998, p. 281; Vega et al., 2004, p. 217 A variety of are known from O. couesiHall and Dalquest, 1963, p. 288; Eckerlin, 2005, p. 155; Underwood et al., 1986; Barnard et al., 1971, p. 1294 and the marsh rice ratWolfe, 1982, p. 3 and two parasitic have been found in O. gorgasi.Sánchez et al., 2001, p. 211
The marsh rice rat is the natural reservoir of the Bayou virus, the second most common cause of hantavirus pulmonary syndrome in the United States.McIntyre et al., 2005, p. 1083 Two other hantaviruses, Catacamas virus and Playa de Oro virus, occur in O. couesi in Honduras and western Mexico, respectively, but are not known to infect humans.Milazzo et al., 2006; Chu et al., 2008
Circumscription
The name Oryzomys was introduced in 1857 by Spencer Fullerton Baird for the marsh rice rat (now Oryzomys palustris) of the eastern United States,Baird, 1857, p. 482 which had been first described twenty years earlier by Richard Harlan.Musser and Carleton, 2005, p. 1144 The name combines the Greek oryza "rice" and mys "mouse" and refers to the feeding habits of the marsh rice rat.Schwartz and Schwartz, 2001, p. 192, . Baird placed Oryzomys as a subgenus of the now-defunct genus Hesperomys and included only the marsh rice rat in it, a classification which was followed by Elliott Coues in 1874 and 1877.Coues, 1874, pp. 183–184; 1877, p. 113 In 1890, Oryzomys was raised to generic rank, and in subsequent years numerous additional species were ascribed to it, many of which were soon moved to separate genera.Tate, 1932, pp. 4ff. In the 1898 Catalogus Mammalium, Édouard Louis Trouessart listed 67 species of Oryzomys,Trouessart, 1898, pp. 523–527 including some that are now placed in Calomys, Necromys, Thomasomys, and other genera unrelated to Oryzomys.Tate, 1932, pp. 6–7; Musser and Carleton, 2005, pp. 1105, 1108, 1128, 1130, 1144, 1179, 1180 Some of the new genera proposed were soon subsumed in Oryzomys again,Weksler, 2006, table 1; Musser and Carleton, 2005, p. 1144 and in The Families and Genera of Living Rodents (1941), John Ellerman listed Microryzomys, Oligoryzomys, Melanomys, Nesoryzomys, and Oecomys as synonyms of OryzomysEllerman, 1941, p. 340 and included about 127 species in it.Ellerman, 1940, pp. 345–359 In 1948, Philip Hershkovitz suggested that other oryzomyines like Nectomys and Megalomys could as well be included in Oryzomys,Hershkovitz, 1948, p. 54, footnote 1 and Clayton Ray followed this suggestion in 1962.Ray, 1962, pp. 16–26
Species
The current concept of Oryzomys derives from the palustris-mexicanus group recognized within a much larger genus Oryzomys by Merriam (1901) and the palustris group proposed by Goldman (1918).Carleton and Arroyo-Cabrales, 2009, p. 116 Merriam recognized 21 species within his group, but Goldman consolidated them into eight—the marsh rice rat in the United States, Oryzomys couesi in far southern Texas, Mexico, and Central America, and six others with small distributions.Goldman, 1918, p. 16 In 1960, Raymond Hall united O. couesi and the marsh rice rat into a single species, Oryzomys palustris, and thereafter, other localized forms were also included in O. palustris.Musser and Carleton, 2005, p. 1147 Hershkovitz described another species in the group, Oryzomys gorgasi from Colombia, in 1970Hershkovitz, 1970, p. 700 and the next year he noted that O. dimidiatus, previously classified as a Nectomys, was similar to O. palustris.Hershkovitz, 1971, pp. 789, 791 After 1979, the marsh rice rat and O. couesi were again regarded as separate as a result of further work in Texas, where their ranges meet. While reviewing O. gorgasi in 2001, J. Sánchez H. and colleagues redefined and characterized the O. palustris group and listed O. couesi, O. dimidiatus, O. gorgasi, and the marsh rice rat as its members;Sánchez et al., 2001, pp. 209–210 Guy Musser and Michael Carleton in the 2005 third edition of Mammal Species of the World additionally listed Oryzomys nelsoni from María Madre Island in western Mexico.
Oryzomys albiventer Michoacán, Guanajuato, Jalisco (inland western Mexico)Carleton and Arroyo-Cabrales, 2009, pp. 118 Large, long tail, robust skull Described in 1901 as a species; subspecies of O. couesi in 1918; reinstated as a species in 2009Carleton and Arroyo-Cabrales, 2009, pp. 117–118 Oryzomys antillarum Jamaica (extinct)Morgan, 1993, p. 439 Long , short incisive foramen (perforations in the palate), robust (cheekbones)Goldman, 1918, p. 44 Described in 1898 as a species; subspecies of O. couesi in 1966; reinstated as a species in 1993/2006Morgan, 1993, p. 439; Weksler et al., 2006, table 1, footnote e Oryzomys couesi Southern Texas and coastal Sonora (northwestern Mexico) to northwestern ColombiaMusser and Carleton, 2005, p. 1147; Carleton and Arroyo-Cabrales, 2009, p. 119 Upperparts to reddish, underparts white to buff, sphenopalatine vacuities small to absentGoldman, 1918, p. 29 Described in 1877 as a species; subspecies of marsh rice rat in 1960; reinstated as a species in 1979; various other species split from and lumped into it from time to time.Musser and Carleton, 2005, p. 1147; Carleton and Arroyo-Cabrales, 2009, pp. 94–95 Genetic data suggest four species may be present: one along the Pacific coast from Sonora to El Salvador; one from Texas to Nicaragua; one in Costa Rica; and one in Panama.Hanson et al., 2010, pp. 342–343 Oryzomys dimidiatus Southeastern NicaraguaMusser and Carleton, 2005, p. 1148 Gray underparts, brown feet, tail nearly the same color above as belowReid, 2009, p. 207 Described in 1905 as a species of Nectomys; reclassified in Oryzomys in 1948Hershkovitz, 1948, pp. 54–55 Oryzomys gorgasi Northwestern Colombia, northwestern Venezuela; extinct on CuraçaoMusser and Carleton, 2005, p. 1149; Voss and Weksler, 2009, p. 73 Robust rostrum (front part of skull); incisive foramina tapering at the back; sphenopalatine vacuities absent; subsquamosal fenestra (opening at the back of the skull) smallSánchez et al., 2001, p. 210 Described in 1970; Oryzomys curasoae described in 2001; both synonymized in 2009 Oryzomys nelsoni María Madre Island, Nayarit, western Mexico (extinct)Musser and Carleton, 2005, p. 1152 Large, long tail, rostrum heavy and bent downward, large and wideCarleton and Arroyo-Cabrales, 2009, pp. 121–122 Described in 1898 as a species; subspecies of O. palustris in 1971; otherwise regarded as a distinct species Marsh rice rat ( Oryzomys palustris) In the eastern United States from New Jersey and Kansas south to Florida and Texas, and into Tamaulipas, Mexico; previously further north to Iowa and southwestern PennsylvaniaMusser and Carleton, 2005, p. 1152; Schmidt and Engstrom, 1994, p. 914; Richards, 1980, fig. 1 Compared to sympatry O. couesi where the two meet: short tail, white underparts, sphenopalatine foramen largeSchmidt and Engstrom, 1994, p. 917 Described in 1827; specific status of Florida Keys form ( argentatus; first described in 1978) disputed;Musser and Carleton, 2005, p. 1153 genetic data suggest populations west of Alabama may be a separate speciesHanson et al., 2010, p. 342 Oryzomys peninsulae Southern tip of Baja California Sur (perhaps extinct)Carleton and Arroyo-Cabrales, 2009, p. 114 Moderately large, gray on head and forequarters, broad, squared zygomatic arches, long, broad incisive foramina, upper incisor nearly orthodontCarleton and Arroyo-Cabrales, 2009, p. 122 Described in 1899 as a species; subspecies of O. palustris in 1971 and of O. couesi in 1994; reinstated as a species in 2009
Description
Oryzomys contains medium-sized, semiaquatically specialized oryzomyine rodents. They have long, coarse fur that is grayish to reddish on the upperparts and white to buff on the underparts.Goldman, 1918, p. 19; Reid, 2009, p. 206; Carleton and Arroyo-Cabrales, 2009, p. 116 The marsh rice rat superficially resembles the introduced species black rat and brown rat, but has larger differences in color between the upper- and underparts. The (whiskers) are short and the ears are small and well-haired. The tail is usually as long as or longer than the head and body and is sparsely haired, but the hairs on the lower side are longer than those above. Females have eight mammae, as in most oryzomyines. The hindfeet are broad and have the first and fifth digits notably shorter than the middle three. The upper surface is hairy, but the underside is naked and covered with small irregularities (squamae). The pads are generally poorly developed, as are the ungual tufts.Goldman, 1918, p. 19; Reid, 2009, p. 206; Carleton and Arroyo-Cabrales, 2009, p. 116; Sánchez et al., 2001, p. 209 Interdigital webbing may be present, but its development is variable within the genus.
+ Measurements of species of Oryzomys 36.1 (33–40) 29.3 (28–30) 30.5 (27–33) 28.3 (27–31) 31 (30–32) 37.3 (35–39) 28–37 32.0 (29–34) Measurements are in millimeters and in the form "average (minimum–maximum)".
Distribution, ecology, and behavior
The range of Oryzomys extends from New Jersey in the eastern United States through Mexico and Central America south to northwestern Colombia and east to northwestern Venezuela and Curaçao.Carleton and Arroyo-Cabrales, 2009, p. 116; Voss and Weksler, 2009, p. 73 Species of Oryzomys usually live in wet habitats such as marshes, streams, and , but both the marsh rice rat and O. couesi are also occasionally encountered in drier habitats.Reid, 2009, p. 207; Kruchek, 2004, p. 269 They occur or occurred on many continental-shelf islands and one oceanic island, Jamaica; their adeptness at colonizing islands may be caused by their close association with water and frequent occurrence in coastal wetlands. The oldest fossils date to the Rancholabrean of the United States, about 300,000 years ago; although there have been some earlier North American records, those are not in fact referable to Oryzomys or even Oryzomyini.Weksler, 2006, pp. 87–88 Oryzomyines likely evolved in South America east of the Andes; the presence of Oryzomys in Central America and other trans-Andean regions is thought to be the result of one of several independent invasions of this region by oryzomyines.Weksler, 2006, p. 88 Alternatively, Oryzomys may have evolved from the Pliocene North American Jacobsomys.Lindsay, 2008, p. 473 O. antillarum may have reached Jamaica during the last glacial period while sea levels were low.
Human interactions
Two species of Oryzomys, O. antillarum and O. nelsoni, have gone extinct since the 19th century,Morgan, 1993, p. 239; Musser and Carleton, 2005, p. 1152 and a third, O. peninsulae, is unlikely to be still extant. Their extinction may have been caused by habitat destruction and by introduced species such as the small Asian mongoose and the brown and black rat.Morgan, 1993, p. 239; Ray, 1962, pp. 33–34; Carleton and Arroyo-Cabrales, 2009, pp. 114–115 These same causes may threaten O. gorgasi, which the IUCN Red List assesses as "Endangered".Sánchez et al., 2001, pp. 205, 211; Weksler and Timm, 2017 O. albiventer has been affected by human alteration of its habitat, but likely still survives.Carleton and Arroyo-Cabrales, 2009, p. 115 In contrast, the widespread species, the marsh rice rat and O. couesi, are common and of no conservation concern—indeed, both have been considered a pest—but some populations are threatened.Linzey and Hammerson, 2008; Linzey et al., 2016; Vega et al., 2004, p. 218; Schmidly and Davis, 2004, p. 281; Whitaker and Hamilton, 1998, pp. 278–280; Hofmann et al., 1990, p. 162 Like these two species, O. dimidiatus is assessed as "Least Concern" by the Red List.Linzey and Hammerson, 2008; Linzey et al., 2016; Timm and Reid, 2019
Notes
Literature cited
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