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Jerboa

Jerboas are small, bipedal belonging to the Dipodinae within the Dipodidae, renowned for their elongated hind limbs that are four times longer than their forelimbs, enabling exceptional jumping abilities across sandy terrains. These nocturnal mammals, typically measuring 5 to 15 centimeters in body length with tails often exceeding their body size, feature large eyes for low-light vision, elongated ears in many species for heat dissipation and hearing predators, and furry soles on their feet to prevent sinking in loose sand. Distributed across arid landscapes from northern Africa through the Middle East to central and eastern Asia, jerboas thrive in hot deserts, steppes, and semi-arid grasslands, where temperatures can exceed 40°C during the day. They construct complex burrow systems—sometimes with multiple chambers for nesting, food storage, and waste—that can extend up to 2.5 meters deep, allowing them to remain cool and protected from predators like owls, foxes, and snakes during daylight hours. Primarily solitary or living in loose colonies, jerboas emerge at night to forage on a diet of seeds, insects, roots, and occasional vegetation, using their short forelimbs to manipulate food and dig shallow foraging pits. With around 33 divided into 13 genera, jerboas exhibit diverse adaptations to extreme environments, such as the ability to survive without free by obtaining from their and producing highly concentrated . Notable examples include the (Euchoreutes naso), with ears comprising half its body length for enhanced sensory detection, and the great jerboa (Allactaga major), capable of leaps up to 3 meters. While most face no major threats, degradation from and poses risks to some populations, though many remain widespread in their native ranges.

Taxonomy and Classification

Etymology and Definition

The term "jerboa" originates from the word yarbuʿ (يَرْبُوع) or jarbūʿ (جَرْبُوع), referring to a small noted for its jumping ability, and was borrowed into New Latin as jerboa in the 1660s. This entered European languages through accounts of travelers and naturalists encountering the animals in and , with the earliest recorded English usage dating to 1662 in a describing their long hind legs and tufted tail. The word is a of "gerbil," reflecting shared linguistic roots in for similar burrowing rodents. Biologically, jerboas are defined as bipedal, saltatorial rodents in the subfamily Dipodinae of the family Dipodidae, adapted to arid habitats with elongated hind limbs that enable leaps up to several times their body length. They differ from related jumping rodents, such as zapodids in the family Zapodidae (North American jumping mice), by their more specialized desert morphology, including reduced forelimbs, fused metatarsals for stability, and a focus on nocturnal, hopping locomotion rather than cursorial movement. The subfamily Dipodinae comprises key genera such as Allactaga (five-toed jerboas, known for their robust builds and burrowing habits), Dipus (northern three-toed jerboas, with slender forms suited to sandy dunes), and Jaculus (lesser Egyptian jerboas, featuring three toes and exceptional jumping prowess). Historically, jerboas were initially classified among other in the expansive family (mice and rats) by early taxonomists like , who described species such as Jaculus jaculus in 1758 under a separate genus but within broader murine groupings. This changed in 1817 when established the family Dipodidae to distinguish jerboas and their allies based on unique cranial features, limb proportions, and ecological specializations, marking a key shift in . Subsequent refinements, driven by morphological and later molecular evidence, have solidified Dipodidae as a distinct lineage within the superfamily , separate from .

Phylogenetic Relationships

Jerboas are members of the family Dipodidae, which includes jerboas (saltatorial subfamilies) and birch mice (Sicistinae), placed within the superfamily of the suborder and order Rodentia. This classification reflects their position among the Myomorpha, a diverse suborder characterized by gnawing incisors and cheek teeth adapted for varied diets. The superfamily comprises the Dipodidae and the Zapodidae (jumping mice), distinguishing it from other myomorph superfamilies like the . Within rodent phylogeny, forms the to , the latter including families such as (African pouched rats and climbing mice) and (hamsters, voles, and rats). This close relationship is supported by shared myomorph cranial and dental features, with divergence between and estimated at approximately 55-60 million years ago in the late to early Eocene, based on recent calibrations incorporating fossil constraints. Within , early diversification is evidenced by fossils like Protalactaga, a genus from the late to early (approximately 25–30 million years ago), which represents primitive members of the subfamily Allactaginae and indicates initial radiations in arid Asian environments. Molecular studies reinforce the evolutionary framework of jerboas, with analyses of , including the cytochrome b gene, confirming the monophyly of the subfamily Dipodinae, which encompasses most true jerboa genera. These genetic data, combined with nuclear markers, resolve internal relationships and highlight Dipodinae's distinct lineage from other dipodid subfamilies like Allactaginae, with divergence within Dipodidae dated to the around 30–35 million years ago. A defining feature of Dipodidae's phylogeny is the presence of key synapomorphies adapted for saltatorial , notably the of hindlimbs relative to and the of size and count. These traits, evident in and extant forms, evolved as adaptations for bipedal hopping in open habitats, distinguishing jerboas from their quadrupedal muroid relatives and underpinning their ecological success in deserts.

Species Diversity

Jerboas encompass approximately 33 species distributed across 13 genera within the family Dipodidae, reflecting significant taxonomic diversity adapted to arid environments. These species are organized into four or five subfamilies depending on the classification: Allactaginae, Dipodinae, Cardiocraniinae, Euchoreutinae, and Paradipodinae (sometimes merged into Dipodinae), each characterized by variations in hindlimb structure and toe count that influence locomotion. For instance, the subfamily Dipodinae primarily includes three-toed jerboas, while Allactaginae features five-toed forms, with Euchoreutes placed in its own subfamily or Dipodinae in some classifications to highlight its distinct long-eared morphology. The genus Allactaga (great jerboas or five-toed jerboas) includes about 6 species, such as the great jerboa (Allactaga major); related genera like Scarturus (3 species, including the Scarturus tetradactyla) contribute to the subfamily's diversity. Other notable genera include Pygeretmus (3 species of fat-tailed jerboas), Salpingotus (pygmy jerboas), and monotypic genera such as Allactodipus and Dipus. Among the most distinctive species is the (Euchoreutes naso), renowned for its oversized ears relative to body size; the Gobi jerboa (Allactaga bullata), a robust form from Central Asian deserts; and the (Salpingotulus michaelis), the smallest jerboa species with adults weighing around 3.2 grams. Recent taxonomic revisions, particularly in the 2020s, have refined jerboa classification through morphological and phylogenetic analyses. For example, studies on three-toed jerboas in Dipodinae have elevated several to full status based on cranial and genetic data, while the genus Scarturus—encompassing small five-toed jerboas—has been delineated more clearly from related taxa like Allactaga following evaluations of dental and skeletal traits. These updates, building on earlier works like Holden and Musser (2005), underscore ongoing refinements in understanding jerboa evolutionary relationships.

Physical Characteristics

External Anatomy

Jerboas, members of the subfamily Dipodinae within the family Dipodidae, display considerable variation in body size across their approximately 33 . Head-body lengths typically range from 4 to 18 cm, with tails measuring 8 to 30 cm—often exceeding the body length—and weights spanning 3 to 400 g, reflecting adaptations to diverse arid environments. Smaller species, such as the thick-tailed pygmy jerboa (Salpingotus crassicauda), have head-body lengths of 4.5–6 cm and weights around 8–10 g, while larger ones like the great jerboa (Allactaga major) reach 18 cm in head-body length and up to 415 g. Their fur is characteristically soft and silky, providing in extreme conditions, with coloration adapted for cryptic in sandy habitats. Dorsal fur is typically pale sandy or yellowish, often accented by darker stripes along the back for blending into arid landscapes, while the ventral side is white or cream. Eyes are large and prominent, suited for nocturnal , and ears vary markedly by ; in long-eared forms like Euchoreutes naso, they can measure up to 5–7 cm—nearly two-thirds of the body length—enhancing heat dissipation and sound detection. Limb morphology is a defining feature, with hindlimbs that are four times as long as their forelimbs, enabling bipedal saltation, while forelegs remain short and vestigial for . Hindfeet 3–5 toes equipped with hairy pads or fringes that prevent sinking into loose sand, and the forelegs, with five digits, primarily facilitate feeding and manipulation. The tail is slender, tufted at the tip with black-and-white hairs, and serves as a counterbalance during leaps reaching up to 3 m in distance.

Internal Adaptations

Jerboas exhibit specialized skeletal adaptations in their hindlimbs that facilitate efficient bipedal and jumping in arid habitats. The tarsal bones, particularly the , are elongated to provide greater leverage for , allowing the animal to store and release effectively during leaps. Additionally, the central three metatarsal bones in larger species fuse into a single rigid structure known as the cannon , which enhances structural integrity and resists bending forces during high-speed hopping. In contrast, the forefeet retain five digits, but these are reduced in size and phalangeal count compared to quadrupedal , adapting them primarily for feeding rather than weight-bearing. Muscular adaptations in jerboas support powerful jumps by optimizing energy storage and release. The is enlarged and paired with an extended , which acts as an elastic mechanism to store during takeoff and return it upon landing, minimizing metabolic cost in oxygen-scarce conditions. This tendon-muscle complex contributes significantly to the jerboa's ability to achieve jumps up to 3 m, with the recovering a portion of the energy expended in vertical leaps. Physiological features enable jerboas to thrive in water-scarce environments through superior conservation mechanisms. Their kidneys are highly efficient, featuring long loops of Henle that allow production of with osmolality exceeding 5000 mOsm/L, far surpassing that of mesic and enabling survival on metabolic alone. Complementing this, the nasal passages include convoluted turbinates that facilitate countercurrent exchange, cooling exhaled air to condense and reabsorb moisture, thereby reducing respiratory loss by up to 70% in hot, dry air. Internally, sensory adaptations enhance predator detection in open deserts. Jerboas possess enlarged auditory bullae—expanded bony capsules enclosing the —that amplify low-frequency sounds, allowing detection of approaching threats like from distances over 100 meters where high-frequency cues dissipate rapidly. This specialization improves sensitivity to infrasonic vibrations and distant calls, critical for nocturnal evasion in sparse vegetation.

Habitat and Distribution

Geographic Range

Jerboas, belonging to the subfamily Dipodinae within the family Dipodidae, occupy a broad geographic range across arid and semi-arid landscapes of the , encompassing northern including the Desert, the , and extending eastward to and . This distribution is confined to the , with no native populations in the or . Their occurrence aligns primarily with the Palearctic , extending into the in northern Africa, where transitions occur along ecological gradients such as the Sahara-Sahel boundary. Endemic highlight regional specificity, such as the (Salpingotulus michaelis), which is restricted to desert dunes and plains in and potentially adjacent . Representative species illustrate key distributional foci: the great jerboa (Allactaga major) inhabits steppes and northern deserts from through to ; the Gobi jerboa (Allactaga bullata) is centered in the arid zones of and ; and the (Jaculus jaculus) ranges widely across , including Egypt, Sudan, and Morocco, as well as into the . Phylogenetic analyses indicate historical westward dispersals from East into West for certain genera like Allactaga, likely facilitated by post-glacial expansions of open habitats following the .

Environmental Preferences

Jerboas, members of the family Dipodidae, predominantly occupy arid biomes such as hot deserts, steppes, and semi-deserts across , Asia, and parts of , where loose, sandy, or gravelly soils facilitate burrowing activities. These environments typically feature stabilized substrates like sand dunes or clay plains, with species showing a preference for areas of low vegetation density that allow quick escape and foraging. For instance, the (Jaculus jaculus) selects sites with medium soil moisture, cohesion, and coarse particle sizes to optimize burrow stability. Within these biomes, jerboas exploit specific microhabitats centered around burrow systems, which are essential for and predator avoidance. Burrow depths vary by species and purpose, typically 20-50 cm in some pygmy jerboas but up to 1.75 m in species like the (Jaculus orientalis) in sandier locales, featuring multiple chambers for nesting, food storage, and waste, constructed in oblique or zigzag patterns to enhance structural integrity in loose soils. They actively avoid rocky or densely vegetated areas, favoring barren or sparsely covered expanses that support rapid excavation and minimal obstruction. Jerboas exhibit high tolerance for extreme climates, thriving in regions with annual rainfall below 250 mm and diurnal temperatures reaching up to 42-50°C, as seen in the Alxa Desert habitats of the Siberian jerboa (Allactaga sibirica), where means hover around 8.3°C but extremes span -36°C to 42°C. Their nocturnal lifestyle aligns with these hot, dry conditions to minimize heat exposure. Ecologically, they co-occur with predators like pallid foxes (Vulpes pallida) and snakes, prompting adaptations in depth and entrance design to deter intrusion and ensure survival.

Behavior and Ecology

Activity Patterns and Locomotion

Jerboas exhibit strictly nocturnal activity patterns, emerging from their burrows shortly after sunset to engage in foraging and other behaviors, with peak activity often occurring in the early night hours before tapering off toward dawn. This temporal niche minimizes exposure to diurnal predators and the intense daytime heat of arid environments, where surface temperatures can exceed 50°C. Studies on species such as the Siberian jerboa (Allactaga sibirica) reveal bimodal activity in spring and summer, with increased trimodal patterns in autumn, all confined to nighttime periods from approximately 19:00 to 07:00. Similarly, the (Jaculus jaculus) demonstrates entrainment to dark phases under varying light regimes, confirming robust nocturnal rhythms that align with cooler evening conditions in hyper-arid habitats. In response to extreme heat or , some jerboa species retreat deeply into burrows, entering periods of reduced metabolic activity akin to estivation to conserve water and energy, though this behavior is less documented than their winter . During colder months, certain species like the Siberian jerboa (Allactaga sibirica) hibernate from early to late March, utilizing insulated winter burrows to survive low temperatures and food scarcity. These seasonal dormancy strategies complement their nocturnal lifestyle, enabling survival in fluctuating climates. Jerboas are specialized for bipedal saltation, a hopping locomotion that dominates their movement across sandy terrains, involving gaits such as symmetric hopping, asymmetric skipping, and faster running to evade predators through erratic, unpredictable trajectories. At low speeds, they alternate to quadrupedal walking using all four limbs for during cautious or burrowing preparation. When threatened, jerboas can achieve jumps of up to 3 m and sustained speeds reaching approximately 3.5 m/s (12.6 km/h) in controlled settings, with field estimates suggesting higher maxima during escapes. This ricochetal saltation relies on elongated hindlimbs, which provide for rapid and direction changes, enhancing predator avoidance in open deserts. Burrowing is a critical component of jerboa and refuge, excavated primarily with forepaws to loosen and hindlimbs to propel it backward, creating complex systems tailored to seasonal needs. Temporary burrows are shallow (10–20 cm deep) and used for short rests during nightly activity, while summer burrows reach 40–60 cm with plugged entrances to retain coolness. Winter burrows are deeper, often exceeding 1 m, featuring nest chambers lined with for during . These multi-type networks facilitate by providing immediate without long-distance travel. The bounding of jerboas optimizes on loose , where bipedal hopping reduces metabolic cost compared to quadrupedal alternatives by minimizing limb sinking and maximizing stride length through elastic storage, though elastic recovery accounts for only about 14% of total savings. Biomechanical analyses indicate that this lowers overall locomotor energy expenditure by up to 20–30% relative to walking in unstable substrates, supporting sustained nocturnal travel in resource-poor s. Such adaptations underscore the evolutionary convergence of hopping in desert mammals for metabolic thrift.

Social Structure and Foraging

Jerboas exhibit a predominantly solitary , with adults typically occupying individual burrows and interacting minimally outside of breeding periods. Males maintain territorial boundaries, often through scent marking and occasional confrontations, while female home ranges may overlap with those of multiple males, facilitating opportunities without forming stable pairs. For instance, in the five-toed pygmy jerboa (Cardiocranius paradoxus), average home ranges span approximately 14,300 m² (1.43 ha), allowing for resource sharing among females in patchy habitats. Temporary loose family groups can form around breeding burrows, particularly involving a female and her offspring, before juveniles disperse to establish independent territories. Foraging in jerboas is characterized by nocturnal, risk-averse strategies adapted to arid environments with unpredictable resources. Individuals engage in patchy , systematically exploiting localized patches or hotspots before returning to , often under cover of darkness to minimize detection by predators. Activity levels decrease significantly under bright , as higher illumination intensifies predation risk from and foxes, prompting jerboas to shift to darker nights or conditions. Some , such as the dwarf fat-tailed jerboa (Pygeretmus pumilio), within systems for later consumption, a that buffers against seasonal shortages and mirrors adaptations in related . Anti-predator vigilance is enhanced through foot-thumping, where jerboas rapidly drum their hind feet to generate seismic signals alerting nearby individuals to threats, often preceding evasive hops. In response to resource scarcity, jerboas undertake short dispersals, relocating up to several kilometers to access better areas during dry seasons or post-hibernation periods. These movements are typically individualistic, with juveniles dispersing farther than adults to avoid . Social interactions remain infrequent and non-aggressive outside , limited to brief encounters at patches; however, males may display heightened territorial aggression during reproductive seasons to secure mates.

Diet Composition

Jerboas exhibit an omnivorous diet primarily composed of , , and occasional green material, with the precise proportions varying by species and environmental conditions. In the Siberian jerboa (Allactaga sibirica), these components—green plant parts, underground plant structures, , and —occur in roughly equal proportions, reflecting an opportunistic feeding strategy adapted to arid habitats. Similarly, the lesser Egyptian jerboa (Jaculus jaculus) consumes roots, grasses, , grains, and , emphasizing -based foods with supplemental protein from arthropods. Species-specific variations highlight dietary specialization; for instance, pygmy jerboas tend to be more insectivorous than their larger relatives. The pallid pygmy jerboa (Salpingotus pallidus) derives approximately 60% of its diet from insects during spring, shifting to 70% seeds in summer, with common seeds including Carex physodes and Eremopyrum orientale. The long-eared jerboa (Euchoreutes naso) is predominantly insectivorous, targeting flying insects such as beetles and grasshoppers detected through auditory cues, with plant matter playing a minor role. Nutritionally, jerboas are adapted to a high-fiber sourced from and , which they process via in the to extract energy from and other complex carbohydrates. This microbial process enables efficient nutrient absorption from fibrous materials that would otherwise be indigestible. Additionally, they derive all necessary metabolically from their food, eliminating the need for free-standing intake and supporting survival in water-scarce deserts. Seasonal shifts in diet composition further optimize nutritional intake; predominate in when availability peaks, providing protein for , while become the focus in summer and winter for sustained amid scarcity.

Communication and Senses

Vocal and Auditory Signals

Jerboas employ a of vocalizations for communication, including high-pitched squeaks emitted as or distress calls during defensive situations or capture. These squeaks serve to signal immediate threats to nearby individuals, often accompanying aggressive displays like tooth-chattering. In addition, species such as produce low-frequency growls or chatters in confrontational contexts, contributing to intraspecific signaling. Non-vocal auditory signals include hind foot drumming, a low-frequency thumping used by jerboas like when encountering unfamiliar conspecifics or potential predators, functioning as a mechanism. This drumming transmits seismic vibrations through the , detectable by others in the vicinity for predator deterrence. Mating chirps, typically softer and repetitive, are observed in behaviors across Dipodidae species, varying in pitch and pattern to attract partners. Auditory adaptations in jerboas feature enlarged bullae and , enhancing sensitivity to low-frequency sounds essential for detecting distant threats in open desert environments. These structures, including a robust and , facilitate efficient transmission of frequencies in the 100-2000 Hz range, aiding communication within burrows where high frequencies attenuate rapidly. Such adaptations support burrow-based signaling, allowing jerboas to perceive conspecific calls or drumming echoes for orientation in dark tunnels. In species like the (Euchoreutes naso), these traits extend to broader auditory acuity, though vocalizations remain primarily within audible ranges without confirmed ultrasonic components.

Visual and Tactile Cues

Jerboas exhibit limited reliance on visual cues for communication, primarily due to their nocturnal lifestyle, which emphasizes other sensory modalities in dim environments. Their large eyes, adapted with expansive pupils to maximize intake, enable effective in low-light conditions but result in poor acuity during daylight hours, making overt visual signaling less practical and potentially hazardous. This adaptation prioritizes detection of predators and prey at night over detailed daytime perception. Tactile cues play a key role in close-range and among jerboas, with facial serving as primary sensors for detecting vibrations, textures, and air movements in burrows or sandy terrains. These vibrissae allow precise maneuvering in complete , facilitating and without visual input. Additionally, tactile communication includes physical during scent marking, where individuals rub cheek glands against substrates to deposit pheromones, combining touch with olfactory signals to delineate territories and convey individual identity. In social contexts, such as occasional pairings, grooming behaviors provide affiliative tactile reinforcement, helping to maintain bonds through mutual cleaning and physical reassurance, though jerboas remain largely solitary outside breeding periods. Tail movements, while crucial for during bipedal , may occasionally serve subtle visual distraction roles during predator pursuits by creating erratic motion in low .

Reproduction and

Mating Behaviors

Jerboas generally exhibit a polygynous , in which pursue and with multiple females during short periods, while females typically with a single per season. This strategy aligns with their solitary, territorial lifestyles, where defend areas that attract females through resource availability. rituals are brief and dynamic, often initiated when a encounters a receptive female. The performs a hopping display around the crouching female, bobbing his body and standing on his hind legs to face her, followed by rhythmic slapping of her body with his forepaws until copulation occurs; the entire sequence typically lasts 30-60 seconds and can be interrupted if the female rejects the advance by chasing the . also employ scent marking to delineate territories, which females assess for quality, such as proximity to food sources and suitability, influencing selection. Breeding is seasonal, occurring primarily in spring and summer in response to environmental cues like rainfall onset, which stimulates growth and availability to support reproduction. Females may produce one to three litters annually during these opportunistic windows, timed to maximize offspring survival in arid habitats.

Gestation and Offspring Care

Jerboas exhibit a period that typically ranges from 25 to 35 days, though this varies across species; for instance, the ( jaculus) has a gestation of approximately 25 days, while the pallid pygmy jerboa (Salpingotus pallidus) gestates for 30 to 35 days. Litters generally consist of 2 to 6 precocial or semi-precocial young, with averages around 3 to 5 per birth; the ( orientalis), for example, produces litters averaging 3 young, ranging from 2 to 8. Births occur in protected natal burrows, where females construct shallow chambers lined with vegetation for safety and warmth. Offspring are altricial in many species, born hairless, blind, and helpless, requiring intensive maternal care; pygmy jerboas, such as the five-toed pygmy jerboa (Cardiocranius paradoxus), exhibit particularly dependent young that remain hairless and immobile for extended periods post-birth. In contrast, some larger species like the Euphrates jerboa (Allactaga euphratica) produce young that open their eyes shortly after birth and become mobile within days, though full development for bipedal hopping takes several weeks. Females provide exclusive , with males absent due to the solitary nature of jerboas; nursing lasts 3 to 4 weeks, after which occurs around 4 to 6 weeks, as seen in J. jaculus where young are weaned at 6 weeks. Offspring achieve between 8 weeks and 2 months, transitioning to solitary foraging; for J. jaculus, this ranges from 8 to 10 weeks, while pygmy species like S. pallidus reach at about 35 days. is typically reached at 8-12 months in species like J. jaculus, or earlier at around 14 weeks in some pygmy jerboas. Juvenile mortality is high in , often exceeding 50% due to predation and environmental stressors, contributing to the species' r-selected reproductive strategy with multiple litters per season. Lifespans average 2 to 4 years in , limited by harsh conditions, but can extend to 6 years or more in , as recorded for J. jaculus up to 6.4 years.

Conservation

Population Status

Jerboas, belonging to the family Dipodidae, encompass approximately 33 recognized , with 39 assessments on the as of 2024, the majority classified as Least Concern due to their wide distributions in arid and semi-arid habitats across and . For instance, the great jerboa (Allactaga major) is rated Least Concern, reflecting a relatively secure status despite localized pressures. However, certain endemic or range-restricted face higher risks; the (Allactaga tetradactyla) is classified as , indicating insufficient data for a full threat assessment. Population trends among jerboas are generally stable in core desert ranges but show declines in fragmented or peripheral areas, as indicated by recent IUCN assessments. Comprehensive global population estimates for the family are unavailable due to the nocturnal habits and remote habitats of these , though rough extrapolations from regional surveys suggest totals in the millions across all combined. like the northern three-toed jerboa (Dipus sagitta) exhibit stable populations, while others, including the small five-toed jerboa (Scarturus elater), are decreasing. The serves as the primary monitoring tool, with assessments updated periodically; for example, evaluations as of 2024 revealed no significant category shifts for most jerboa species, maintaining their overall low risk. Regional variations are notable, with populations in showing declines in several species compared to more stable trends in North African ranges. Pygmy jerboas, such as the (Salpingotulus michaelis), remain , highlighting gaps in population data for these smaller, less-studied taxa.

Threats and Protection

Jerboas face significant threats from habitat loss driven by , , and , which degrade the arid and semi-arid environments essential for their survival. In , livestock grazing has been documented to reduce vegetation cover and negatively impact the body mass, abundance, and overwinter survival of the northern three-toed jerboa (Dipus sagitta), contributing to localized population declines. Similarly, activities disturb desert habitats, exacerbating fragmentation for species like the Gobi jerboa (Allactaga bullata), which is classified as Least Concern by the IUCN but experiences ongoing degradation in its range. Feral domestic cats pose an additional predation risk, particularly in areas where human settlements encroach on natural habitats, leading to increased mortality among vulnerable nocturnal . Climate change further compounds these pressures by altering rainfall patterns and intensifying drought conditions, resulting in shrinking suitable habitats for jerboas across their distribution. Projections indicate that the Siberian jerboa's potential range in and could contract significantly under future warming scenarios, with upward shifts in elevation potentially limiting access to optimal foraging grounds. Human-induced threats include illegal trapping for the international , which targets charismatic such as the (Euchoreutes naso), classified as Least Concern by the IUCN as of 2024 despite ongoing collection pressures and habitat loss from and . Additionally, secondary from rodenticides used to control outbreaks in central endangers non-target wildlife, including jerboas that consume contaminated prey or bait. Conservation efforts focus on habitat protection and legal safeguards to mitigate these risks. In , approximately 21% of the Gobi jerboa's range falls within protected areas, such as the Great Gobi Strictly Protected Area (), which encompasses over 9 million hectares and supports key populations through anti-poaching patrols and monitoring. The has been legally protected since 2009, with prohibited across most range countries, though enforcement remains challenging in remote desert regions. Recent initiatives, including the Wildlife Conservation Society's 2023 core monitoring program in the Mongolian Gobi, involve camera trapping and population surveys to track jerboa distributions and inform strategies. Ongoing research highlights gaps in understanding , particularly the potential for hybridization between cryptic jerboa species in overlapping ranges, which could undermine adaptive traits in changing environments. Updated genomic studies are needed to evaluate risks, as evidenced by historical hybridization events in North African jerboas like Jaculus jaculus and J. hirtipes.

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