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Dipodoidea

Dipodoidea is a superfamily of rodents within the order Rodentia and suborder Myomorpha, established by Fischer de Waldheim in 1817, encompassing the single family Dipodidae with 52 extant species across 16 genera and 6 subfamilies.^[1] These rodents, commonly known as birch mice, jumping mice, and jerboas, are distinguished by their specialized adaptations for saltatorial (jumping) locomotion, including elongated hind limbs that can be up to four times the length of the forelimbs, fused tarsal bones in the feet, and long, tufted tails for balance and steering during leaps.^[2] Ranging in size from 4 to 25 cm in body length, they exhibit a hystricomorphous skull structure with an enlarged infraorbital foramen and a dental formula typically of 1/1:0/0:0-1/0-1:3/3, adapted for a diet of seeds, insects, and vegetation.^[2] The superfamily Dipodoidea is the sister group to the diverse Muroidea (mice and rats) within the infraorder Myodonta, with fossil evidence tracing their origins to the Middle Eocene epoch, around 45 million years ago, and a more substantial record from the Oligocene.^[3] While some older classifications split Dipodidae into separate families such as Sminthidae (birch mice), Zapodidae (jumping mice), and Dipodidae sensu stricto (jerboas), modern taxonomy, including that of the Integrated Taxonomic Information System (ITIS), recognizes a unified family structure under Dipodoidea to reflect phylogenetic relationships supported by molecular data.^[1]^[4] The subfamilies include Allactaginae (jerboas), Cardiocraniinae (pygmy jerboas), Dipodinae (three-toed jerboas), Euchoreutinae (birch mice), Sicistinae (birch mice), and Zapodinae (jumping mice), highlighting the group's evolutionary divergence into quadrupedal, facultatively bipedal, and obligately bipedal forms.^[1]^[5] Geographically, dipodoids are distributed across the Northern Hemisphere, with jumping mice (Zapodinae) primarily inhabiting grasslands and forests of North America and eastern Asia, birch mice (Euchoreutinae and Sicistinae) favoring Eurasian woodlands and meadows, and jerboas (Allactaginae, Cardiocraniinae, and Dipodinae) thriving in arid deserts and steppes from northern Africa to central Asia.^[2] These nocturnal, fossorial species construct burrows for shelter and hibernation or estivation, with behaviors varying by group: birch mice are agile climbers and runners, jumping mice hibernate for up to nine months, and jerboas can leap up to 3 meters using their powerful hind legs to evade predators and forage efficiently in sparse environments.^[2] Ecologically, they play key roles in seed dispersal and insect control, though many species face threats from habitat loss and climate change in their fragmented ranges.^[3]

Taxonomy

Historical classification

The family Dipodidae, encompassing jerboas, jumping mice, and birch mice, was first established by Gotthelf Fischer de Waldheim in 1817, based on morphological characteristics such as elongated hind limbs adapted for saltatorial locomotion.^[6] Early classifications in the 19th century built upon this foundation, with George Robert Waterhouse refining the family in 1842 to include genera like Dipus and Jaculus, emphasizing dental patterns and cranial structures as key diagnostic traits.^[6] By the late 19th century, Elliott Coues introduced the subfamily Zapodinae in 1875 for North American jumping mice, highlighting subtle differences in auditory bullae and limb proportions, though the group remained unified under Dipodidae.^[6] In the early 20th century, taxonomists generally treated all dipodoids as a single family, Dipodidae, incorporating jerboas (e.g., Allactaga), jumping mice (Zapus), and birch mice (Sicista) based on shared morphological features like reduced forelimbs and specialized tarsal bones.^[7] This unified view persisted through works such as Joel Asaph Allen's 1901 description of subfamilies Sicistinae and Euchoreutinae, which focused on pelage and skeletal similarities without proposing familial splits.^[6] The classification emphasized overall bipedal adaptations and myomorphous jaw musculature, aligning Dipodidae within the suborder Myomorpha. Key revisions occurred between the 1940s and 1970s, driven by detailed morphological analyses. J.R. Ellerman's 1940 and 1961 monographs, along with Ellerman and T.C.S. Morrison-Scott's 1951 checklist, consolidated the family by integrating subfamilies like Allactaginae (Vinogradov, 1925) and Cardiocraniinae, stressing cranial morphology and dental occlusal patterns as evidence of close affinities.^[7]^[8] These works rejected earlier proposals for separate families, such as Weber's 1928 Sicistidae, in favor of a monophyletic Dipodidae supported by comparative osteology.^[6] The recognition of Dipodoidea as a distinct superfamily emerged in the mid-20th century, formalized by George Gaylord Simpson in 1945, who grouped the family within Myomorpha based on integrated dental and cranial features like high-crowned molars and elongated auditory bullae.^[9] Further refinements in the 1980s, such as Pavlinov and Rossolimo's 1987 elevation of Allactagidae, reinforced this status through advanced studies of skull proportions and jaw mechanics, though the core superfamily delineation remained morphologically grounded.^[6] This pre-molecular framework set the stage for later phylogenetic revisions into three families.

Modern phylogeny

The superfamily Dipodoidea was elevated within the suborder Myomorpha during the 1990s, with molecular evidence from mitochondrial DNA sequences supporting its distinction from Muroidea while confirming their close sister-group relationship, forming the clade Myodonta.^[10]^[9] This framework was bolstered by analyses of mitochondrial genes, which highlighted shared synapomorphies in DNA structure and evolutionary rates among dipodoid lineages.^[11] Note that while some classifications, such as that of the Integrated Taxonomic Information System (ITIS), retain a single family Dipodidae with six subfamilies, molecular phylogenetic studies support recognizing three extant families within Dipodoidea: Dipodidae (jerboas; 13 genera, 33 species), Sminthidae (birch mice; 1 genus Sicista, 14 species), and Zapodidae (jumping mice; 2 genera, 5 species), totaling 16 genera and around 52 species.^[12]^[13] These families exhibit monophyly supported by genetic data, with Dipodoidea as a whole forming a robust clade sister to Muroidea.^[9] A key study by Michaux et al. (2004) using the 12S rRNA mitochondrial gene confirmed this monophyly and resolved basal relationships among dipodoid genera, emphasizing convergent morphological adaptations over deep genetic divergences.^[14] Sminthidae and Zapodidae are not subdivided into subfamilies. Within Dipodidae, the family is divided into four subfamilies: Allactaginae (five-toed jerboas), Cardiocraniinae (pygmy jerboas), Dipodinae (three-toed jerboas), and Euchoreutinae (long-eared jerboa), reflecting adaptations to arid environments through saltatorial locomotion. Phylogenetic analyses integrating nuclear and mitochondrial markers have refined these subdivisions, showing Dipodinae as the most diverse and basal within the family. Overall, these genetic insights contrast with earlier morphology-based views by establishing Dipodoidea's position through cladistic and molecular clock methods.^[9]

Physical characteristics

Morphology

Dipodoids are characterized by a compact, rodent-like body form, with head-body lengths typically ranging from 4 to 26 cm across the superfamily, though smaller species like birch mice and jumping mice measure 6–10 cm while larger jerboas reach up to 26 cm; their tails are often longer than the head-body length, providing balance and sensory functions.^[15]^[16] Forelimbs are short and adapted for digging or handling food, contrasting with the more elongated hindlimbs that support saltatorial locomotion.^[3] Dipodoids exhibit a hystricomorphous skull with an enlarged infraorbital foramen, a feature shared with other myomorph rodents.^[2] The dentition of dipodoids follows the myomorph rodent pattern, with a dental formula of I 1/1, C 0/0, P 0–1/0, M 3/3 (×2), yielding 16 or 18 teeth in total; Zapodinae retain an upper premolar (P 1/0) absent in most other subfamilies of Dipodidae, and the molars are rooted with crowns ranging from brachydont to semi-hypsodont and complex occlusal patterns suited for grinding tough vegetation and seeds.^[16]^[17]^[18] Fur varies by subfamily: soft and dense in the woodland-adapted birch mice (Sicista) and jumping mice (Zapus, Napaeozapus), providing insulation, while coarser and sparser in desert-dwelling jerboas, frequently showing countershading with pale sandy dorsal pelage and white ventral fur for concealment against arid substrates.^[19]^[3] Sensory structures reflect their predominantly nocturnal lifestyle, including large, prominent eyes that enhance low-light vision and elongated vibrissae (whiskers) on the snout for tactile navigation through burrows or vegetation.^[20] Sexual dimorphism is generally minimal, with subtle differences in body size—males occasionally slightly larger than females in certain jerboa species like Jaculus—but no consistent cranial or skeletal disparities across the group.^[21] These baseline anatomical traits underpin further specializations, such as hindlimb modifications for jumping.

Locomotion adaptations

Dipodoidea exhibit remarkable adaptations for saltatorial locomotion, primarily through modifications in their hindlimbs and associated structures that enable efficient jumping and rapid evasion in arid or open habitats. In jerboas (Allactaginae, Cardiocraniinae, Dipodinae), the hindlimbs are profoundly elongated, with hind feet measuring approximately 2–3 times the length of forefeet, conferring significant leverage for propulsion during bipedal movement. This elongation is complemented by the fusion of the central three metatarsals into a robust cannon bone, which resists bending forces and enhances stability under high ground reaction loads during hopping, allowing for sustained dynamic locomotion without structural failure.^[22]^[23] The foot morphology in jerboas further optimizes bipedal hopping, featuring enlarged digital pads divided by cross folds for improved traction on loose substrates, alongside a prominent central pad at the base of the third digit that aids in shock absorption. Toe reduction to three or four functional digits on the hind feet minimizes drag and focuses force transmission through the fused metatarsals, facilitating explosive leaps. In contrast, jumping mice (Zapodinae) retain a pentadactyl foot structure that is cursorial, supporting bipedal hops over short distances while permitting quadrupedal walking for foraging.^[24]^[25]^[16] The long, tufted tail in jerboas plays a critical role in maintaining balance and stability during high-speed maneuvers, acting as a counterweight to prevent forward pitching in mid-air and enabling sharp directional changes. Leaps supported by these adaptations can span up to 3 meters horizontally, providing an effective escape mechanism from predators. Birch mice (Sicistinae), with their shorter tails, rely less on extreme saltation and instead use the tail for enhanced agility in quadrupedal scampering, incorporating occasional bounds to navigate dense vegetation.^[26]^[27] Muscular and tendinous enhancements underpin the power output of these locomotor strategies, particularly in jerboas where the gluteal muscles are enlarged to drive hip extension, and the Achilles tendon exhibits high compliance for energy storage and recoil during vertical and horizontal propulsion. These features collectively enable burst speeds reaching up to 10.8 km/h (180 m/min) in certain species, such as the comb-toed jerboa, though sustained locomotion often involves variable gaits like hopping, skipping, and bounding to optimize efficiency. In jumping mice, similar but less pronounced muscular adaptations support intermittent bipedal hops of 1–2 meters, while birch mice favor steady quadrupedal progression with supplementary leaps for evasion.^[28]^[29]^[26]

Distribution and habitat

Geographic range

Dipodoidea species are primarily distributed across the Palearctic and Nearctic realms of the Northern Hemisphere. The superfamily's range encompasses diverse biomes from deserts and steppes to forests, reflecting adaptations to varied environments in these regions.^[7] Subfamilies Allactaginae, Cardiocraniinae, and Dipodinae (jerboas) occupy extensive areas from North Africa eastward through the Middle East, Central Asia, and into Mongolia and northern China. Euchoreutinae and Sicistinae (birch mice) are widespread across Eurasia, extending from Europe and the Caucasus through Siberia, the Kazakh steppes, Tian Shan mountains, Altai region, and Mongolia to China. Zapodinae (jumping mice) are confined mainly to North America—from Alaska and Canada southward to the central and western United States—with a disjunct extension to eastern Asia in central China via the genus Eozapus.^[7]^[2]^[13] The collective geographic range of Dipodoidea covers vast expanses, underscoring their prominence in northern terrestrial ecosystems. Highest species diversity occurs in the arid steppes of Kazakhstan and Mongolia, where multiple genera of jerboas, such as Stylodipus and Allactaga, coexist and contribute to elevated local richness.^[30]^[31] Disjunct distributions characterize the superfamily, with jumping mice entirely absent from Europe and birch mice predominantly restricted to temperate forest belts rather than open arid zones. Recent climate change has prompted range shifts in some populations, including upward shifts amid overall habitat contraction for the Siberian jerboa (Orientallactaga sibirica) in parts of its Asian range, evidenced by modeling predictions and observations from the 2000s onward.^[32]

Habitat preferences

Dipodoids exhibit diverse habitat preferences shaped by their subfamilies. Members of the Dipodinae (jerboas) predominantly occupy arid and semi-arid zones, including deserts, sand dunes, and steppes characterized by sparse vegetation cover. These environments, often featuring loose sandy or stabilized clay substrates, are prevalent across the southern Palearctic, with notable examples in the hyper-arid Gobi Desert where species like the Gobi jerboa thrive amid extreme dryness.^[33]^[34] Jerboas favor microhabitats suitable for burrowing, such as loose sand for constructing extensive tunnel systems that provide refuge from diurnal heat and predators.^[33] In contrast, the Zapodinae (jumping mice) and Sicistinae (birch mice) prefer more mesic temperate habitats, including woodlands, grasslands, meadows, and taiga regions with dense understory vegetation. Jumping mice, such as the meadow jumping mouse (Zapus hudsonius), select moist riparian zones, grassy fields, and areas bordering streams or marshes with high herbaceous cover for nesting and foraging.^[35] Birch mice (Sicista spp.) inhabit forested edges, subalpine grasslands, and tall-herb communities in transitional zones between forests and meadows, often in slightly disturbed areas with rich herbage.^[36] These groups utilize microhabitats like leaf litter and subterranean burrows for hibernacula, where nests of grass and dead leaves offer insulation during prolonged dormancy.^[37]^[35] Across Dipodoidea, altitudinal ranges span from sea level to over 4,000 m, with some jerboa species, such as the Siberian jerboa (Orientallactaga sibirica), reaching high-altitude arid plateaus on the Tibetan Plateau in Central Asia, while jumping and birch mice occur up to subalpine elevations around 2,000 m in regions like the Appalachians and Caucasus.^[38]^[39]^[36]^[37] Many dipodoids demonstrate tolerance to temperature extremes from -40°C in continental winters to 50°C in desert summers, facilitated by physiological adaptations and behavioral strategies such as deep burrowing or hibernation.^[40] Certain jerboa populations move to ungrazed areas post-hibernation to access fresher resources amid fluctuating environmental conditions.^[40]

Behavior and ecology

Diet and foraging

Dipodoids exhibit an omnivorous diet, with seeds and vegetation forming the primary components (typically 70–90% of intake across species), supplemented by insects and occasionally fungi or small vertebrates. In jerboas (Allactaginae, Cardiocraniinae, and Dipodinae), plant matter such as seeds, roots, bulbs, and green vegetation dominates, accounting for 89–99% of the diet, while insects contribute only 1–11% on average. Jumping mice (Zapodinae) consume a mix of seeds, fruits, fungi, and arthropods, with arthropods comprising up to 50% in some analyses of gut contents. Birch mice (Euchoreutinae and Sicistinae) show greater insect reliance, particularly in summer when invertebrates can make up the majority of their intake for protein, alongside seeds, berries, and green plant parts.^[41]^[16] Foraging occurs predominantly at night, leveraging heightened senses like olfaction to detect food sources on the surface or in shallow soil. Jerboas employ bipedal hops to glean seeds and insects from desert floors, relying on their acute sense of smell to locate buried or scattered items without extensive digging. Birch mice use their elongated, flexible snouts to probe leaf litter and soil for insects and seeds, facilitating precise extraction in grassy or forested understories. Jumping mice forage in herbaceous vegetation, climbing stems to access fruits and fungi, often detected via olfactory cues. While some dipodoids scatter-hoard seeds near burrows, jumping mice rarely cache food, instead relying on pre-hibernation fat accumulation from high-energy foraging bouts.^[42]^[43]^[16] Dietary habits vary seasonally to optimize nutrition and energy conservation. In summer, consumption shifts toward insects and fungi for protein and fats, as seen in jumping mice where lepidopterans and dipterans appear consistently, alongside early-season sedges and late-season forbs. Winter foraging emphasizes calorie-dense seeds and roots, with reduced activity; many species enter torpor or hibernation, lowering metabolic rates to as little as 5% of normal and minimizing food needs during scarcity. For instance, birch mice increase seed intake pre-hibernation, losing up to 30% body mass over winter but emerging to insect-rich diets.^[44]^[45] As seed dispersers, dipodoids inadvertently aid plant propagation by dropping or burying uneaten seeds during foraging, enhancing germination in arid or steppe ecosystems, as observed in jerboas sifting soil for bulbs. Their predation on insects positions them as controllers of arthropod populations, regulating pest levels in grasslands and deserts while supporting trophic balance. These roles underscore their ecological importance, though overgrazing can disrupt foraging efficiency.^[46]^[47] Reproduction in Dipodoidea is typically seasonal, occurring primarily during spring and summer months, with females producing one to three litters per year in response to increasing photoperiod lengths that signal favorable environmental conditions. In jerboas (Allactaginae, Cardiocraniinae, and Dipodinae), such as Jaculus jaculus, breeding seasons span March to August in natural habitats, though captive individuals may breed more frequently every three months. In jumping mice (Zapodinae), like Zapus princeps, mating begins shortly after emergence from hibernation in late spring, extending from late April to early September, with up to two or three litters possible in a single season. In birch mice (Euchoreutinae and Sicistinae), breeding occurs from May to August with typically one litter per year.^[48]^[49]^[50] Litter sizes in Dipodoidea generally range from 2 to 9 young, with averages of 3 to 6 depending on the species and environmental factors; for instance, jerboas average 3 young in Jaculus jaculus, jumping mice average 5.4 (ranging 2–9) in Zapus species, and birch mice typically 3–6 (up to 11 in some Sicista species). Gestation periods vary from 18 to 35 days across the superfamily, lasting 25–30 days in many jerboas such as Jaculus jaculus, approximately 18 days in jumping mice like Zapus princeps, and 23–30 days in birch mice. Young in all groups are born altricial—hairless, blind, and helpless—requiring extended care in underground burrows lined with vegetation; in jerboas, this includes prolonged maternal investment to develop bipedal locomotion skills, with independence achieved at 8–10 weeks.^[48]^[51]^[49]^[52]^[53]^[54] Parental care is predominantly provided by females, who nurse and protect offspring in secure burrows, provisioning them until weaning at around 3–5 weeks; males exhibit territorial behavior but do not participate in direct paternal care in most species. In jerboas, females may aggressively evict young from nests post-weaning, while in jumping mice, mothers transport altricial young by mouth if disturbed. Hibernation in some jumping mice and birch mice species can delay or truncate breeding cycles by limiting the active period for reproduction.^[48]^[55]^[49] Social structure in Dipodoidea is largely solitary, with individuals maintaining exclusive home ranges outside of brief breeding interactions, though loose colonies form in certain jumping mice habitats like riparian zones. Jerboas are strictly solitary year-round except during mating, using scent marking and visual displays for territory defense. Birch mice are also predominantly solitary. Mating systems are predominantly polygynous, particularly in jerboas, where males compete through scent marking and upright postures to court multiple females, as observed in Jaculus jaculus and Stylodipus telum; in jumping mice, systems may also be polygynous, with males sharing nests with multiple females and offspring in some cases.^[56]^[48]^[57]^[54]

Evolutionary history

Fossil record

The fossil record of Dipodoidea documents a diverse group of rodents originating in Asia during the Middle Eocene, approximately 48–37 million years ago (mya), with subsequent dispersals to Europe and North America. The earliest known fossils come from Asian localities, such as the genus Primisminthus from the middle Eocene of central China (Henan and Shanxi provinces), which exhibits primitive dental features including low-crowned, bunolophodont molars adapted for a mixed diet in forested environments.^[58] Similarly, Banyuesminthus from contemporaneous deposits in China shares these early traits, marking the initial radiation of dipodoids from ancestral myomorph rodents.^[3] Over 20 extinct genera have been described, highlighting the superfamily's evolutionary breadth across continents. Notable examples include Banyuesminthus (Eocene, China), Protalactaga (early to middle Miocene, Europe and Asia, with five-toed hindlimbs indicating transitional bipedal adaptations), and Armintomys (middle Eocene, North America, featuring retained premolars and early ricochetal morphology).^[3] Other key taxa encompass sicistines like Heosminthus and Plesiosminthus (late Eocene to Oligocene, Asia and Europe) and zapodines such as Megasminthus (Miocene, North America).^[59] The temporal distribution of Dipodoidea fossils spans the Eocene to the Pleistocene, with peak diversity occurring during the Miocene (approximately 23–5 mya), when multiple lineages diversified in aridifying Asian steppes and spread westward.^[3] Major fossil-bearing sites include the Oligocene Tabenbuluk fauna in western Gansu Province, China, which has yielded several genera such as Shamosminthus and Gobiosminthus, reflecting early community assemblages in transitional woodlands.^[60] In North America, the Pliocene Blacktail Cave deposits in Montana preserve zapodine remains, including forms related to modern jumping mice, amid late Cenozoic faunal turnovers.^[61] Extinction patterns indicate a significant decline in European dipodoid diversity following the Pleistocene, linked to post-glacial climate warming and habitat fragmentation that favored more adaptable competitors over specialized saltatorial forms.^[3] While Asian and North American lineages persisted, European sicistines and early jerboas largely vanished by the Holocene, underscoring the role of climatic shifts in shaping modern distributions.^[62]

Phylogenetic relationships

Dipodoidea, a superfamily within the suborder Myomorpha of Rodentia, occupies a basal position in the myomorph lineage, forming a sister group to the more diverse superfamily Muroidea. This relationship has been consistently supported by molecular phylogenetic analyses using nuclear and mitochondrial genes, placing the divergence between Dipodoidea and Muroidea in the late Paleocene to early Eocene, approximately 50–60 million years ago (mya). Genomic studies from the 2010s, incorporating multi-locus datasets, further affirm this topology, with Dipodoidea branching off early within Myomorpha, distinct from other suborders like Sciuromorpha and Caviomorpha.^[63]^[64] Within Dipodoidea, phylogenetic reconstructions based on nuclear genes such as BRCA1, RAG1, GHR, and IRBP reveal a resolved tree where the subfamily Sicistinae (birch mice) represents the basal lineage, followed by Zapodinae (jumping mice), with the jerboa subfamilies (Allactaginae, Cardiocraniinae, Dipodinae) as the more derived clades under the unified family Dipodidae. This intra-superfamily structure, supported by concatenated sequence data from multiple genera, indicates monophyly for each subfamily, though resolution among certain subfamilies within the jerboas (e.g., Dipodinae, Allactaginae, and Euchoreutinae) remains a trichotomy in some analyses. A 2025 study discovered an ancient Himalayan birch mouse lineage (new genus Breviforamen), confirming Sicistinae as the basal extant group and extending their evolutionary history across the Qinghai-Xizang Plateau region.^[65] Eocene fossils like Simimys from North America are integrated as stem-dipodoids, providing early evidence of myomorph traits such as elongated hindlimbs, while Miocene radiations, including genera like Protalactaga and Tamquammys, bridge the gap to extant jerboas, reflecting adaptations to arid environments. Divergence time estimates, calibrated with fossil constraints, date the origin of Dipodoidea to around 40–43 mya in the middle Eocene, coinciding with global cooling and habitat shifts that favored cursorial forms. Subsequent subfamily-level splits occurred between 34 and 27 mya during the Oligocene, with Sicistinae diverging first, followed by the Zapodinae-jerboa subfamilies split; further diversification within the jerboa subfamilies accelerated in the late Miocene (11–8 mya), aligning with the expansion of grasslands. Controversies persist regarding the monophyly of Zapodinae, as some morphology-based phylogenies nest its genera (e.g., Zapus and Napaeozapus) within the jerboa subfamilies, though molecular data strongly support its independence as a sister clade to the jerboas.

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Zapus hudsonius (meadow jumping mouse) - Animal Diversity Web
They are generally nocturnal (although occasionally diurnal), and usually move in sequential short hops of about 2.5 to 15 cm or by crawling along vole runways ...Missing: bipedal | Show results with:bipedal
[35]
(PDF) Recent geographic distribution of birch mice (genus Sicista) in ...
This report focuses on the faunal results of a mammalogical expedition, aimed to survey distribution, habitat preference, current density, ...
[36]
Napaeozapus insignis (woodland jumping mouse) | INFORMATION
Woodland jumping mice have 16 total teeth and a dental formula of 1/1, 0/0, 0/0, 3/3. Northern populations average 12% larger in body size than southern ...
[37]
Original biological and ecological data on the endemic Chinese ...
It belongs to the Dipodidae family (Zapodinae sub-family) (Wilson and Reeder, 2005), among which the monotypic genus Eozapus is endemic to central China (Wilson ...
[38]
Activity strategy and pattern of the Siberian jerboa (Orientallactaga ...
Mar 10, 2021 · A pattern has emerged in some studies to show that abiotic environmental factors such as temperature often provide a range within which rodents ...
[39]
Dipodidae. ( ⁉ ⁉ ) ''Coming through! This unusual ... - Facebook
Dec 3, 2023 · ... jerboas to migrate to ungrazed areas during post-hibernation. Grazing negatively impacts the Jerboa pre- and post- hibernation population ...The thick-tailed pygmy jerboa (Salpingotus crassicauda ... - FacebookJerboas' remarkable desert hopping adaptations explainedMore results from www.facebook.com
[40]
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[41]
Allactaga euphratica (Euphrates jerboa) - Animal Diversity Web
Jerboas have keen senses of hearing, smell, and vision in dim light. As with other rodents, they probably communicate among themselves using mainly olfactory ...
[42]
Learn about Animals - Mammal Web
Northern birch mouse. Scientific name: Sicista betulina. Appearance: Yellow ... The head is long and elongated with a flexible snout which enables it to ...<|separator|>
[43]
breadth and seasonal variation in the diet of the New Mexico ...
Jumping mice survive annual hibernations of up to 9 months on body fat rather than seed caching (Humphries et al. 2003; Frey 2015) and the provision of seed ...
[44]
Preble's Meadow Jumping Mouse (Zapus hudsonius preblei)
The U.S. Fish and Wildlife Service later designated critical habitat for the Preble's meadow jumping mouse in 50 CFR 17.68 on June 23, 2003, and revised ...Missing: temperature | Show results with:temperature
[45]
Jaculus orientalis (greater Egyptian jerboa) - Animal Diversity Web
When the animal sifts through the soil searching for seeds and other plant matter, it disperses seeds, particularly those too hard to eat, and aerates the soil.
[46]
Effects of overgrazing on the functional diversity of rodents in desert ...
Feb 21, 2024 · The species composition in the summer was only significantly correlated with the functional traits of reproductive cycle and diet. (2) The ...
[47]
Jaculus jaculus (lesser Egyptian jerboa) - Animal Diversity Web
Sexual Dimorphism; female larger. Range mass: 43 to 73 g: 1.52 to 2.57 oz. Average mass: 55 g: 1.94 oz. Range length: 95 to 110 mm: 3.74 to 4.33 in. Average ...<|control11|><|separator|>
[48]
Zapus princeps (western jumping mouse) - Animal Diversity Web
Western jumping mice are found primarily in moist fields, thickets, and woodlands, especially where grasses, sedges, or other green plant cover is dense.
[49]
Meadow Jumping Mouse - Montana Field Guide
Sep 24, 2024 · There are 18 teeth in the skull (dental formula: I 1/1, C 0/0, P 1/0 ... Body measurements are: total length 187 to 255 millimeters ...
[50]
[PDF] Capture d'écran 2019-01-18 à 16.28.19 - ORBi
Jan 18, 2019 · 1 species Vulnerable; none Extinct since 1600. Systematics. The superfamily Dipodoidea (Rodentia, Myomorpha) is the sister group of Muroidea ...<|control11|><|separator|>
[51]
https://orbi.uliege.be/bitstream/2268/231835/1/texte%2520total%2520chapitre%2520dipodidae%2520handbook%2520mammals%2520species%2520of%2520the%2520world.pdf
[52]
[PDF] J. F. EISENBERG
Dipodomys the social system appears to be predicated on individual defense of a burrow system and defense of associated caches. A Comparison of Behavior ...
[53]
SUNY ESF Meadow Jumping Mouse
216pp. Order: Rodentia Family: Zapodidae. Range and Habitat. The range is the southern half of Alaska, most of Canada, and the eastern two-thirds of the U.S. ...Missing: geographic distribution
[54]
SPATIAL ORGANIZATION OF STYLODIPUS TELUM (DIPODIDAE ...
suggesting a promiscuous or polygynous mating system. Individuals used a single day burrow and several shelter burrows. Use of day burrows was exclusive ...
[55]
Molecular and Paleontological Evidence for a Post-Cretaceous ...
The earliest known fossils of Dipodinae (three-toed jerboas) is dated to 10.5 Ma ... earliest fossil record of myodonts [19]. Based on recent magneto ...
[56]
Dipodidae (Mammalia, Rodentia) from the Paleogene of south-east ...
Oct 28, 2019 · The Dipodidae described in this paper are part of the late Eocene-early Oligocene small mammal assemblages found in south-east Serbia. The ...
[57]
Dipodidae (Rodentia, Mammalia) from the Oligocene and Early ...
Cenozoic sediments and fossils of the Taatsiin Gol and Taatsiin Tsagaan Nuur area in Mongolia yield important information about stratigraphy and mammal ...
[58]
Publications | University of Montana
A new species of petrified cones from the Oligocene of western Montana. American Journal of Botany, Vol. 56 (9), 972-978.
[59]
A small assemblage of early Oligocene rodents and insectivores ...
Feb 8, 2023 · The assemblage of small mammals from a site near Yeniköy (Anatolia) is described. The assemblage was collected by screen-washing a sample from a locality in ...
[60]
A glimpse on the pattern of rodent diversification: a phylogenetic ...
Jun 14, 2012 · Myodonta is divided into Muroidea (BP = 100%) and Dipodidae (BP = 100%). Platacanthomyidae is the sister-group to all other Muroidea [49]. Our ...
[61]
Whole mitochondrial genome sequence and phylogenetic ...
Jul 16, 2020 · The superfamily Dipodoidea formed a sister group with Muroidea, and this relationship has been well demonstrated in previous studies (Holden & ...