Sciurus
Sciurus is a genus of tree squirrels comprising 28 species of small- to medium-sized, arboreal rodents in the family Sciuridae, characterized by their prominent bushy tails, sharp claws, and adaptations for climbing and leaping among trees.[1][2] The name Sciurus derives from the Ancient Greek words skia (shadow or shade) and oura (tail), alluding to the squirrels' habit of resting in tree shade with their tail arched over their back. These diurnal mammals typically exhibit no sexual dimorphism in size or coloration, with body lengths ranging from 20 to 50 cm (excluding the tail) and weights between 200 and 1000 grams depending on the species.[2] Established taxonomically by Carl Linnaeus in 1758, the genus belongs to the tribe Sciurini within the subfamily Sciurinae and includes seven subgenera, such as Sciurus, Guerlinguetus, and Otosciurus, encompassing 142 subspecies in total.[1] Species of Sciurus are distributed across the Palearctic, Nearctic, and Neotropical realms, ranging from Eurasia and North America through Central America to northern South America, where they inhabit diverse forested habitats including deciduous woodlands, coniferous forests, and tropical rainforests.[3] Notable species include the Eurasian red squirrel (S. vulgaris), the eastern gray squirrel (S. carolinensis), and the fox squirrel (S. niger) in North America, as well as various Neotropical forms like the red-tailed squirrel (S. granatensis).[1] These squirrels play key ecological roles as seed dispersers and prey for predators, though some species face threats from habitat loss and competition with introduced populations.[3]Taxonomy
Etymology and Classification History
The genus name Sciurus derives from the ancient Greek words skia, meaning shadow or shade, and oura, meaning tail, a reference to the animal's behavior of sitting in the shade cast by its bushy tail.[4] Carl Linnaeus formally established the genus Sciurus in the 10th edition of Systema Naturae published in 1758, designating Sciurus vulgaris—the Eurasian red squirrel—as the type species based on specimens from Europe.[4][5] Early post-Linnaean naturalists classified Sciurus within the family Sciuridae, with Thomas Pennant providing influential descriptions of squirrel morphology and distribution in his 1771 work Synopsis of Quadrupeds, which helped solidify the family's boundaries amid growing collections from Europe and North America.[6] Throughout the 19th century, classifications refined further through the efforts of systematists like John Edward Gray, who in publications such as his 1867 Synopsis of the species of American squirrels in the collection of the British Museum and related zoological arrangements organized Sciurus species by cranial and dental traits, incorporating specimens from global expeditions to address variability in pelage and size.[7][8] By the early 20th century, Sciurus was firmly recognized as a distinct genus within the order Rodentia, encompassing tree squirrels across multiple continents, with taxonomic reviews estimating approximately 40 species based on morphological distinctions before later consolidations reduced recognized counts through synonymy.[6] Key revisions in the 1940s, including those by Glover Morrill Allen in his multi-volume The Mammals of China and Mongolia (1938–1940), grouped Sciurus taxa by geographic ranges and osteological features, influencing North American and Asian classifications.[9] In the 1970s, Ronald M. Nowak advanced these frameworks in contributions to mammalian taxonomy, such as co-authored accounts in Mammalian Species, by emphasizing subgeneric divisions to better reflect evolutionary affinities among species.[10]Phylogenetic Relationships
The genus Sciurus first appears in the fossil record during the Middle Miocene, approximately 15 million years ago, with isolated cheek teeth attributed to the genus recovered from localities in Anatolia (modern-day Turkey) and other parts of Europe, as well as early records in North America.[11] These fossils indicate that Sciurus was already a distinct arboreal form by this time, co-occurring with other early sciurids in forested environments. A notable North American example is Sciurus olsoni from the Late Miocene of Nevada, representing one of the earliest well-documented species and highlighting the genus's initial diversification across Holarctic regions. Within the Sciuridae family, Sciurus belongs to the tribe Sciurini, which encompasses tree squirrels and diverged from ground squirrel lineages (subfamily Xerinae) around 30–40 million years ago during the late Eocene to early Oligocene, coinciding with the expansion of forested habitats in North America. Phylogenetic analyses place Sciurus as part of a monophyletic Sciurini clade, with the North American red squirrels (Tamiasciurus) as the sister group to Sciurus sensu lato, reflecting an early split within the tribe that underscores the genus's Holarctic origins before subsequent dispersals.[12] This placement is supported by both morphological comparisons of fossil postcrania, which show shared arboreal specializations like elongated tarsals for leaping, and molecular data confirming the tribe's unity separate from flying squirrels (Pteromyini). Molecular phylogenies have refined the evolutionary history of Sciurus, with a 2004 study by Steppan et al. using nuclear genes (c-myc and RAG1) demonstrating the monophyly of Sciurus based on sequences from multiple genera, highlighting its distinct radiation within Sciurini. More recent mitogenomic analyses, such as the 2020 work by de Abreu-Jr et al., incorporated complete mitochondrial genomes from 40 Sciurini species and revealed hidden diversity, rendering Sciurus paraphyletic and prompting proposals to elevate subgenera like Leptosciurus for certain Neotropical lineages with slender tails and specialized gliding traits. These studies estimate the crown age of Sciurini at around 20 million years ago, with key divergences driven by vicariance and dispersal events. The evolutionary adaptations of Sciurus, including enhanced grasping limbs, large eyes for depth perception, and flattened tails for balance during arboreal locomotion, are linked to the Eocene radiation of angiosperms (flowering plants), which created complex canopy structures and diverse nut-bearing trees approximately 50–40 million years ago, favoring specialized tree-dwelling rodents over ground-dwellers. A major divergence within Sciurus separates the Neotropical clade, which colonized South America via the Great American Biotic Interchange, from the Holarctic clade, with molecular clocks estimating this split at 10–15 million years ago during the Miocene, influenced by cooling climates and Andean uplift that fragmented forests.[13] This event facilitated rapid speciation in the Neotropics, adapting to tropical diversity while Holarctic forms emphasized caching behaviors in temperate zones.Subgenera and Species Recognition
The genus Sciurus is traditionally subdivided into seven subgenera, a classification established in the comprehensive revision by Thorington and Hoffmann (2005), which organized the then-recognized 28 species based on morphological, distributional, and preliminary genetic evidence.[6] These subgenera include Sciurus (sensu stricto), encompassing Holarctic species such as the Eurasian red squirrel (S. vulgaris), characterized by temperate forest adaptations; Guerlinguetus, comprising Neotropical lowland forms like the Guayaquil squirrel (S. aestuans); and Urosciurus, featuring montane species such as the Andean squirrel (S. pyrrhinus), distinguished by elongated tails and high-elevation distributions.[6] The remaining subgenera—Otosciurus, Hesperosciurus, Hadrosciurus, and Tenes—further delineate regional clades, with Hesperosciurus limited to western North American species like the western gray squirrel (S. griseus) and Tenes including the Caucasian squirrel (S. anomalus) adapted to Eurasian woodlands.[6] Species recognition within Sciurus relies on a combination of morphological traits, genetic markers, and behavioral signals to establish diagnosability and reproductive isolation. Morphological criteria often focus on diagnostic features such as relative tail length, presence of ear tufts, cranial proportions, and pelage patterns, which help differentiate closely related taxa in overlapping ranges.[14] Genetic analyses, particularly sequencing of the mitochondrial cytochrome b gene, have been instrumental in resolving phylogenetic boundaries and identifying cryptic diversity, though nuclear markers are increasingly incorporated for more robust delimitation.[15] Vocalizations also play a role in species identification, with distinct alarm calls and territorial chirrs serving as acoustic barriers that reinforce genetic and morphological distinctions, especially in sympatric Neotropical assemblages.[16] In conservation contexts, IUCN assessments incorporate minimum viable population thresholds—typically estimated at 1,000–5,000 mature individuals for least concern status—to evaluate taxonomic validity alongside threat levels, ensuring recognized species maintain ecological viability.[17] Recent taxonomic revisions have significantly altered the scope of Sciurus by elevating subgenera to full genera and proposing new splits based on molecular phylogenies. In their 2015 review of South American Sciuridae, de Vivo and Carmignotto elevated several subgenera (e.g., Guerlinguetus, Hadrosciurus, Urosciurus) to generic rank, restricting the core Sciurus to approximately 15–17 primarily Holarctic and northern Neotropical species while redistributing the remaining 11–13 to new or revived genera.[18] This restructuring emphasized biogeographic barriers and genetic divergence, reducing paraphyly in the original genus. Further refinements occurred in a 2020 mitogenomic study by de Abreu-Jr et al., which proposed reorganizing Sciurini into 14 genera and 46 species, restricting Sciurus sensu stricto to the three Eurasian species (S. anomalus, S. lis, S. vulgaris) and elevating or creating genera such as Neosciurus for North American grays (S. carolinensis) and Parasciurus for larger forms like the fox squirrel (S. niger), while excluding species like the fiery squirrel (S. flammifer)—previously in subgenus Hadrosciurus—to the genus Syntheosciurus based on deep mitochondrial divergences and phenotypic convergence.[15] As of 2025, these proposals remain influential but not fully adopted in all taxonomic authorities, which continue to recognize 28 species in Sciurus.[19] This highlights the need for integrative taxonomy in montane clades. Despite these advances, significant gaps persist in the taxonomic framework for Sciurus, particularly for poorly sampled Neotropical species. For instance, species such as the Yucatán squirrel (S. gilvigularis) and Sanborn's squirrel (S. sanborni) lack comprehensive genetic data, with no published cytochrome b sequences or whole-genome analyses available, resulting in provisional placements within subgenera Guerlinguetus and reliance on outdated morphological descriptions.[20] This scarcity of molecular evidence contributes to ongoing debates about their specific status and relationships, underscoring the need for targeted field collections to resolve provisional classifications.[15]Physical Description
General Morphology
Sciurus species exhibit a slender, elongated body adapted for arboreal locomotion, featuring strong hind limbs that enable powerful jumps between branches and pentadactyl feet equipped with sharp, curved claws for gripping tree bark.[21] Unlike flying squirrels in the tribe Pteromyini, tree squirrels lack a patagium, relying instead on their limb structure and tail for stability during descent.[22] The forefeet possess four elongated digits plus a reduced thumb, while the hind feet have five toes, all padded with soft, furred soles that provide traction on rough surfaces.[23] The tail is characteristically bushy and cylindrical, often nearly as long as the body, with dense fur that covers it from base to tip and aids in thermoregulation by trapping air.[24] In cross-section, the tail appears slightly flattened due to the arrangement of its vertebrae and surrounding musculature, which supports its role in maintaining balance during movement.[24] The skull is elongated and robust, housing a dentition typical of sciuromorph rodents, with a total of 22 teeth following the formula I 1/1, C 0/0, P 2/1, M 3/3. Prominent, ever-growing incisors facilitate gnawing on hard materials, while the molars feature prismatic cusps suited for grinding tough plant matter.[25] Sensory adaptations include large, forward-facing eyes that provide binocular vision suited to diurnal activity, enhancing depth perception in forested environments.[21] Prominent vibrissae on the muzzle and cheeks serve as tactile sensors for navigating narrow branches and detecting nearby obstacles.[26] Acute hearing is supported by rounded ears positioned high on the head, allowing detection of low-frequency sounds from predators or conspecifics.[27] Internally, Sciurus possess a simple, glandular stomach for initial breakdown of ingested material, complemented by a large caecum that hosts microbial communities for fermenting fibrous plant components through hindgut fermentation.[28] This digestive configuration enables efficient processing of seeds, nuts, and other vegetation central to their diet.[28]Size, Coloration, and Sexual Dimorphism
Species in the genus Sciurus exhibit a moderate range in body size, with head-body lengths typically spanning 200–500 mm and tail lengths from 150–300 mm across adults. Weights generally fall between 200 g and 1000 g, though Neotropical species tend to be smaller, such as S. richmondi averaging around 250 g.[29] These measurements reflect adaptations to arboreal lifestyles, with longer tails aiding balance, though exact proportions vary by species and region.[30] Fur coloration in Sciurus is diverse but follows a common pattern of grizzled gray, reddish-brown, or cinnamon tones on the dorsal surface, contrasted by white, cream, or buff ventral pelage.[30] Temperate species, like S. carolinensis, undergo two annual molts, producing a denser winter coat for insulation and a sleeker summer pelage. Melanistic forms occur in several populations, notably black morphs in S. carolinensis and S. niger, resulting from genetic variations in melanin production.[31] Sexual dimorphism in Sciurus is minimal, with no significant differences in overall size, coloration, or pelage patterns between males and females in most species.[30] Males may exhibit slightly greater body mass in some cases, such as up to 10% heavier in S. niger, but this is not consistent across the genus.[2] Females possess more developed mammary glands to support lactation, though external morphology remains monomorphic. Intraspecific variation in Sciurus often manifests as geographic clines in coloration, with darker coats prevalent in humid tropical regions and paler tones in arid zones, as observed in S. niger across its range.[32] Such variations arise from local environmental influences on pelage development, without altering the fundamental dorsal-ventral contrast.[33]Distribution and Habitat
Geographic Range
The genus Sciurus exhibits a broad native distribution primarily within the Holarctic and Neotropical realms, encompassing diverse forested habitats across multiple continents. In the Holarctic region, species of the subgenus Sciurus are predominant, ranging from temperate and boreal forests in Europe and Asia to deciduous and coniferous woodlands in North America. For instance, the Eurasian red squirrel (S. vulgaris) occupies a vast area from the United Kingdom and Ireland eastward through continental Europe to the Ural Mountains in Russia and further into northern Asia, extending to Mongolia, China, and Japan, spanning latitudes up to approximately 70°N.[34][35] In North America, species such as the eastern gray squirrel (S. carolinensis) are native from southern Canada through the eastern and midwestern United States to northern Mexico, while the fox squirrel (S. niger) inhabits central and eastern regions of the continent.[36][37] The overall Holarctic range reflects post-glacial recolonization patterns in Eurasia following the Last Glacial Maximum, with ancestral lineages originating in North America around 36 million years ago and subsequent dispersals to Asia.[21][38] In the Neotropics, the subgenera Guerlinguetus and others dominate, with the majority of Sciurus species—approximately 70% of the genus's total diversity—confined to Central America and northern and central South America, from approximately 18°N to 28°S latitude.[21] These species thrive in tropical rainforests, montane forests, and gallery woodlands, with key concentrations in the Amazon Basin and Andean foothills, where diversification hotspots have driven high endemism since the Pliocene, around 6 million years ago. A representative example is the Brazilian squirrel (S. aestuans), which ranges across the Amazon River basin in Colombia, Venezuela, the Guianas, northern Brazil, and extends southward to eastern Paraguay, Bolivia, and northeastern Argentina, often reaching the eastern slopes of the Andes.[21][39][40] The Neotropical radiation likely stemmed from North American ancestors invading northwestern South America, leading to cladogenetic events concentrated in the Pacific domain and subsequent spread across the region.[39][38] Several Sciurus species have established introduced populations outside their native ranges through human-mediated translocations beginning in the 19th century. The eastern gray squirrel (S. carolinensis) was introduced to the United Kingdom in the late 19th century (starting around the 1870s–1890s) from North America, where it has since expanded widely, and to Italy in the 1940s from escaped pets originally imported in the late 1800s; additional introductions occurred in South Africa around 1900 on private estates in Cape Town.[41][42][43] The fox squirrel (S. niger) has been introduced to the Pacific Northwest of the United States, including Washington state in the early 1900s, and California within the past 130 years, with ongoing range expansions in western North America.[44][45] These introductions often followed ornamental or hunting releases, contrasting with the natural historical expansions driven by climate shifts.[41]Habitat Preferences and Adaptations
Species of the genus Sciurus primarily inhabit arboreal environments characterized by the presence of trees, favoring deciduous and coniferous forests, woodland edges, and mixed woodlands across elevations from sea level to approximately 3,000 m. These squirrels select habitats with ample canopy cover and structural complexity to support their arboreal lifestyle, including temperate broadleaf forests in North America and Europe, as well as tropical and montane rainforests in Central and South America. Their distribution spans diverse ecosystems such as swampy areas and riparian zones, provided suitable trees are available for locomotion and shelter.[21][46] Within these habitats, Sciurus species exhibit key morphological and behavioral adaptations for arboreal life. Flexible ankle joints allow the hind feet to rotate nearly 180 degrees, enabling head-first descent down tree trunks by splaying the feet against the bark for grip. The long, bushy tail functions as a counterbalance during climbing and leaping between branches, while also serving as a rudder to aid steering and stability during jumps spanning up to several meters. Sharp, curved claws on all feet provide secure attachment to bark, facilitating rapid vertical and horizontal movement through the canopy. Behaviorally, these squirrels are highly agile, capable of precise calculations for inter-tree leaps, and they preferentially use microhabitats near mast-producing trees such as oaks (Quercus spp.) and hickories (Carya spp.), where acorns and nuts provide essential resources. Nesting occurs in tree cavities for protection during winter or in external dreys—large leafy nests constructed in tree forks—for summer use, often at heights of 5–20 m to minimize predation risk.[47][46] Sciurus demonstrates remarkable tolerance to environmental disturbance and habitat fragmentation, thriving in human-altered landscapes including suburban gardens and urban parks. This adaptability is evident in species like the eastern gray squirrel (S. carolinensis), which readily occupies city greenspaces and exploits anthropogenic food sources such as bird feeders, maintaining populations in highly fragmented areas. In urban settings, they select microhabitats with dense understory and tall trees for cover, showing reduced flight responses to human presence compared to rural conspecifics. Climatically, Sciurus species do not hibernate but remain active year-round, entering short bouts of torpor—a state of reduced metabolic rate and body temperature—during extreme cold to conserve energy when food is scarce. In tropical ranges, activity persists without significant estivation, though rare instances occur under seasonal resource shortages. These traits underscore their resilience across varied climatic zones, from boreal winters to equatorial conditions.[48][49][50]Behavior and Ecology
Diet and Foraging Strategies
Sciurus species exhibit a primarily herbivorous diet, with nuts, seeds, and fruits comprising the majority of their intake depending on habitat and season. Acorns from oak species (Quercus spp.), hickory nuts (Carya spp.), and pine seeds (Pinus spp.) serve as staple foods, providing high-energy mast that supports survival during periods of scarcity. They occasionally consume animal matter such as insects, fungi, bird eggs, or small vertebrates when preferred plant resources are limited.[51][52][23] Foraging activity in Sciurus is diurnal, with peaks at dawn and dusk to minimize predation risk while maximizing efficiency. Individuals scan visually from tree canopies to locate food sources, then descend to ground level or remain arboreal to harvest items such as cones or mast. Seasonal shifts influence preferences: in spring, when seeds are scarce, squirrels consume tree buds, flowers, and young shoots; summer foraging targets fungi and soft fruits; and autumn focuses on high-fat mast accumulation. In coniferous habitats, species like the Eurasian red squirrel (S. vulgaris) spend up to 93% of winter foraging time extracting pine seeds from cones using strong incisors and dexterous paws.[53][51] A hallmark foraging strategy is scatter-hoarding, where individuals bury thousands of small caches annually—up to 5,000-10,000 in eastern gray squirrels (S. carolinensis)—to store surplus food for winter. Squirrels retrieve a substantial portion of their caches (typically 40-95%, depending on conditions), but many are pilfered by other animals or left uneaten, benefiting seed germination and thus influencing forest dynamics. Caches are placed near visual landmarks like trees or rocks to aid relocation, with olfactory cues playing a critical role in detection even under snow or soil. Eastern fox squirrels (S. niger), for instance, prioritize larger, higher-fat items during hoarding to optimize energy returns, aligning with optimal foraging principles.[54][55][56][57] Nutritional adaptations enable efficient exploitation of challenging foods. Sciurus species select mast with high lipid content, such as white oak acorns (up to 20% fat), over lower-quality alternatives. To counter tannins in red oak acorns (5-15% concentration), which inhibit digestion, gray squirrels rely on specialized gut microbiota for detoxification and improved protein digestibility, conferring a competitive edge over species like red squirrels. These microbes facilitate tannin breakdown, allowing consumption of tannin-rich foods without significant physiological cost.[56][58]Reproduction and Development
Most species of Sciurus exhibit a polygynandrous mating system, in which females mate with multiple males and males compete for access through behaviors such as scent marking and chasing rivals.[36][27] This promiscuous strategy results in multiple paternity within litters, enhancing genetic diversity while allowing males to maximize reproductive opportunities without long-term pair bonds.[59] Breeding patterns in Sciurus vary by latitude and habitat. In boreal and temperate species, such as the Eurasian red squirrel (S. vulgaris) and eastern gray squirrel (S. carolinensis), reproduction is seasonal, with typically 1-2 litters per year produced in late winter to spring (December-February) and early to mid-summer (May-July), timed to coincide with peak food availability for lactation.[34][36] In contrast, tropical and subtropical species, like the Yucatan squirrel (S. yucatanensis), often breed continuously or show peaks during rainy seasons, potentially producing up to 3 litters annually under optimal conditions.[60] Gestation lasts 38-45 days across the genus, with an average litter size of 2-5 young (typically 3), though ranges can extend to 1-7 depending on species and maternal condition.[27][34][60] Young Sciurus are altricial at birth, emerging hairless, blind, and weighing 8-18 g, requiring intensive maternal care in secure nests.[36][27] Eyes open after 4-5 weeks, weaning occurs at 7-10 weeks, and juveniles achieve independence shortly thereafter, reaching sexual maturity at 9-12 months.[34][36] Wild lifespan averages 6-12 years, though most individuals do not survive to adulthood due to predation and environmental factors.[27][34] Parental care is provided solely by females, who nurse, groom, and protect offspring, often relocating litters to avoid threats; males play no role after mating.[21][36] Infanticide by unrelated males is rare but documented in high-density populations, such as in S. vulgaris, where it may accelerate female estrus during resource-abundant periods like mast years.[61]Social Structure and Communication
Sciurus species exhibit primarily solitary social organization, with individuals maintaining individual home ranges that often overlap, particularly between sexes. Females are typically territorial year-round, defending exclusive core areas against other females to secure resources, while males display greater range overlap and territorial behavior primarily during breeding seasons. In Eurasian red squirrels (Sciurus vulgaris), female core areas show minimal intrasexual overlap (around 9-10%), whereas male ranges overlap more extensively (up to 44%), reflecting sex-specific strategies for resource access and mating opportunities.[62] In eastern gray squirrels (Sciurus carolinensis), social hierarchies structure interactions, with older, larger males dominating subordinates, and females asserting priority when protecting litters, though overall home ranges (0.4-2.4 ha) commonly overlap without strict boundaries.[63] Group dynamics are loose and transient, with individuals occasionally forming small aggregations of 2-10 during mast years when food abundance reduces competition. In winter, dreys may be shared among related females or mother-offspring groups for thermoregulation, promoting limited communal nesting in species like S. vulgaris, though such sharing is infrequent and temporary. Territorial behaviors include agonistic displays such as chases, vocal threats, and physical confrontations involving bites, often escalating in resource-scarce conditions. Density influences these interactions; in urban habitats, populations reach up to 18-31 squirrels per hectare with increased tolerance for proximity due to supplemental resources, compared to 1-5 per hectare in natural forests where territorial defense is more intense.[64][65] Communication among Sciurus individuals occurs through multiple modalities to convey alarm, aggression, mating interest, and territorial claims. Vocalizations include alarm calls such as the sharp "kuk" barks and rattling sounds in S. carolinensis for aerial or terrestrial threats, and trills during mating chases; S. vulgaris employs similar barks and chatters for defense.[66] Chemical signaling involves scent marking via cheek gland rubbing on branches and trunks, as well as urine and fecal deposits at posts, which advertise sex, dominance, and reproductive status to deter intruders or attract mates.[67] Visual cues feature prominently in agonistic contexts, with tail positioning—such as tight curling to signal aggression or partial bending for submission—modulating chase intensity and fight outcomes in S. carolinensis.[68] Ear twitching and upright postures further enhance these displays, facilitating rapid assessment of intent during encounters.Species Diversity
Current List of Recognized Species
The genus Sciurus currently comprises 28 recognized species according to standard taxonomy (as of 2025), including those in seven subgenera such as Sciurus, Guerlinguetus, and Otosciurus, with 142 subspecies in total.[1] These species are primarily arboreal tree squirrels characterized by bushy tails, strong claws for climbing, and varied pelage patterns adapted to forested habitats across the Holarctic and Neotropics. A complete list is provided in Thorington et al. (2012); below is a table of selected recognized species, including brief identifying traits, geographic ranges, and IUCN conservation statuses.| Scientific Name | Common Name | Identifying Traits | Geographic Range | IUCN Status |
|---|---|---|---|---|
| S. anomalus | Caucasian squirrel | Grayish-brown fur with white underparts and black ear tufts in winter; body length ~25 cm, tail ~22 cm. | Southwestern Asia from Turkey to Iran and the Caucasus. | Least Concern (LC) |
| S. vulgaris | Eurasian red squirrel | Reddish-brown fur, prominent ear tufts, white belly; body length 19–23 cm, tail 15–20 cm, mass 250–340 g. | Europe and northern Asia, from UK to Japan. | Least Concern (LC) |
| S. lis | Japanese squirrel | Similar to S. vulgaris but smaller, with grayer fur and less pronounced ear tufts; body length ~20 cm. | Japan (Honshu, Kyushu, Shikoku). | Least Concern (LC) |
| S. aberti | Abert's squirrel | Tufted ears, gray fur with white underparts and rusty accents; body length 23–28 cm, mass ~600 g. | Southwestern United States (Arizona, New Mexico) in ponderosa pine forests. | Least Concern (LC) |
| S. carolinensis | Eastern gray squirrel | Gray fur with white belly, occasional melanistic forms; body length 23–28 cm, tail 19–24 cm, mass 400–700 g. | Eastern and central North America, introduced in parts of Europe. | Least Concern (LC) |
| S. niger | Fox squirrel | Largest in genus, rusty red or gray fur, white-tipped tail; body length 25–30 cm, mass up to 1 kg. | Eastern and central North America. | Least Concern (LC) |
| S. griseus | Western gray squirrel | Silvery-gray fur, white underparts, long tail; body length 26–30 cm, mass 700–1000 g. | Western United States (California, Oregon, Washington). | Near Threatened (NT) |
| S. arizonensis | Arizona gray squirrel | Gray fur with yellowish tinge, white belly; body length 25–28 cm. | Southeastern Arizona and Mexico (Sonora). | Least Concern (LC) |
| S. aureogaster | Mexican gray squirrel | Dark gray fur, pale underparts; body length 23–27 cm. | Central Mexico. | Least Concern (LC) |
| S. deppei | Deppe's squirrel | Gray-brown fur with black head stripe, white belly; body length 22–25 cm. | Southern Mexico to Nicaragua. | Least Concern (LC) |
| S. alleni | Allen's squirrel | Reddish-brown fur, white underparts; body length 25–29 cm. | Western Mexico (Nayarit to Oaxaca). | Least Concern (LC) |
| S. yucatanensis | Yucatan squirrel | Gray fur with orange tones, white belly; body length 24–27 cm. | Yucatan Peninsula (Mexico, Belize, Guatemala). | Least Concern (LC) |
| S. colliaei | Collie's squirrel | Spiny pelage on back, gray-brown fur; body length 22–25 cm. | Western Mexico (Sinaloa to Guerrero). | Least Concern (LC) |
| S. granatensis | Red-tailed squirrel | Variegated gray fur, red-black tail; body length 20–25 cm. | Central America from Mexico to Panama, northern South America. | Least Concern (LC) |
| S. variegatoides | Variegated squirrel | Mottled gray-brown fur, bushy tail; body length 22–26 cm. | Central America (Honduras to Panama). | Least Concern (LC) |
| S. stramineus | Central American squirrel | Pale straw-colored fur, white underparts; body length 21–24 cm. | Costa Rica and Panama. | Least Concern (LC) |
| S. ochraceus | Central American squirrel | Ochre-yellow fur, gray back; body length 23–26 cm. | Nicaragua to Panama. | Least Concern (LC) |