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Shrew

A shrew is a small, insectivorous in the Soricidae, distinguished by its elongated, pointed snout, tiny eyes concealed in fur, small rounded ears, and dense pelage that provides camouflage in leaf litter or undergrowth. These , numbering around 385 across 26 genera, are among the most diverse in the order and represent the smallest terrestrial , with the (Suncus etruscus) weighing as little as 1.2 grams. Shrews inhabit a wide range of environments worldwide, excluding polar regions, , and most of southern , often favoring moist microhabitats such as forests, grasslands, and stream edges, though some adapt to deserts or semi-aquatic lifestyles. Shrews exhibit extraordinarily high metabolic rates—significantly higher than those of similarly sized mammals—necessitating near-constant foraging, as they can starve within hours without food; a single shrew may consume up to twice its body weight daily in invertebrates like insects, worms, and spiders. Some species, notably in the genus Blarina such as the northern short-tailed shrew, possess venomous saliva produced by enlarged submandibular glands, which immobilizes prey larger than themselves, including small vertebrates, marking shrews as one of the few venomous mammalian groups. Behaviorally, shrews are solitary and territorial, active around the clock with bursts of frenzied activity; they may use echolocation-like clicks for navigation in low light and, in aquatic species, propel themselves with specialized bristly tail and foot hairs. Reproduction in shrews is rapid and prolific to counter high mortality, with most species breeding seasonally and litters of 4–8 young after a of 17–24 days; newborns are altricial but develop quickly due to the mother's intense demands. Despite their abundance—shrews often comprise a significant portion of small in ecosystems—they face threats from loss and predation, with few listed as endangered, though their fragile skeletons rarely fossilize, complicating evolutionary studies. Ecologically, shrews play a vital role as predators of soil invertebrates, aiding in and nutrient cycling in temperate and tropical s.

Physical Description

Size and Appearance

Shrews in the family Soricidae exhibit a wide range of body sizes, from the smallest terrestrial , the (Suncus etruscus), with a body length of approximately 3.5 cm and weight of 1.8–2.4 g, to the largest species, the (Suncus murinus), reaching up to 15 cm in body length and 100 g in weight. True shrews possess a mouse-like form distinguished by a long, pointed , small eyes, and tiny, often concealed ears hidden within dense . Their is typically soft and thick, providing with , , or on the upper and lighter gray or silvery tones underneath, while short legs support a scurrying and the is proportionally long—often equal to or exceeding length in many —to aid balance. Skeletal features include the absence of a , resulting in a lightweight, elongated adapted for rapid movements, and sharp, spike-like teeth specialized for piercing tough exoskeletons. The varies slightly across genera but generally follows 3.1.1–3.3 1–2.0–1.1.3, with the upper incisors enlarged and the lower ones often grooved. In some species, such as those in the genus Crocidura, the teeth exhibit red pigmentation due to iron reinforcement in the , enhancing durability against wear. Certain shrews, particularly in the genus Blarina, are venomous, with grooved lower incisors that deliver neurotoxic from submandibular glands to immobilize prey efficiently. This trait underscores their predatory adaptations, though their small size and high metabolic rate limit overall body mass.

Sensory Adaptations

Shrews exhibit limited visual capabilities, primarily due to their small eyes, which are adapted mainly for detecting rather than forming detailed images. This poor eyesight restricts their ability to distinguish fine details or colors, serving largely to differentiate light from dark environments. To compensate, shrews rely heavily on other sensory modalities, such as acute hearing and olfaction, for and prey detection in dense or low-light habitats. A key tactile adaptation is the elongated snout equipped with highly sensitive vibrissae, or , which enable precise detection of prey and obstacles through touch. These macrovibrissae and microvibrissae on the rostrum allow shrews, such as the (Suncus etruscus), to explore surfaces and identify shapes in complete darkness, guiding rapid prey capture behaviors with latencies as short as 80 milliseconds. The vibrissae form a critical sensory array, with cortical representations occupying a significant portion of the dedicated to somatosensory processing. Olfactory senses are highly developed in many shrew species, facilitated by a large nasal chamber and extensive that supports scent detection and territorial maintenance. For instance, the (Blarina brevicauda) possesses the most advanced olfactory organ among North American soricines, correlating with numerous used for active scent-marking to delineate territories and signal . This adaptation aids in locating food sources and avoiding competitors through chemical cues. Shrews demonstrate sensitivity to high-frequency sounds, with hearing ranges extending up to approximately 70 kHz in species like the , enabling detection of subtle environmental noises beyond human auditory limits. Certain species, including the , produce ultrasonic clicks that facilitate echolocation for navigation in confined or dark spaces, such as burrows, by interpreting echo returns without reliance on . These clicks, often emitted in novel environments, help map surroundings and avoid obstacles.

Habitat and Distribution

Geographic Range

Shrews of the family Soricidae exhibit a nearly , inhabiting continents across , , , , and the northern portions of , while being notably absent from , , , polar regions, and the southern extent of . This broad range reflects their adaptability to diverse continental landmasses, with native populations established in temperate and tropical zones where environmental conditions support their insectivorous lifestyle. Diversity within the family is particularly pronounced in regions with varied climates, such as the temperate forests of and , the tropical woodlands of and , and the montane ecosystems of the northern . In , the genus Crocidura dominates, accounting for over 100 species that contribute significantly to the continent's high shrew diversity. hosts more than 70 species, primarily within genera like Sorex and , underscoring the region's role as a hotspot for soricid . Introduced populations have expanded the range of certain species beyond their native habitats, facilitated by human transportation and commerce. The Asian house shrew (Suncus murinus), originally from South and Southeast Asia, has established invasive populations in parts of eastern , , and various Pacific islands, including and , where it often thrives in human-modified environments. Shrews occupy a wide altitudinal gradient, from in coastal lowlands to high-elevation montane zones, with some species adapted to extreme altitudes. For instance, the Mérida small-eared shrew (Cryptotis meridensis) in the northern occurs at elevations ranging from 2,800 to 4,000 meters in habitats, while other records indicate shrew presence up to 4,050 meters in certain Asian and South American highlands. These distributions highlight their tolerance for varied climatic conditions, though specific habitat preferences influence local occupancy.

Preferred Environments

Shrews are primarily terrestrial mammals that inhabit moist, vegetated environments such as forests, grasslands, and wetlands, where they can access abundant prey and maintain suitable humidity levels. These habitats provide the damp conditions essential for shrews, which have high metabolic rates and are prone to in arid areas. Certain species, like the ( brevicauda), favor hardwood forests with deep leaf litter layers that offer cover and foraging opportunities. Within these broader habitats, shrews occupy specific microhabitats including leaf litter, burrows, under-snow spaces, and occasionally hollows, which provide protection from predators and environmental extremes. Their preference for high-humidity microhabitats helps mitigate water loss through their permeable and elevated rates. Some , such as the montane shrew (Sorex monticolus), are adapted to riparian zones and wet meadows within coniferous forests, where moist supports their burrowing activities. Environmental adaptations enable shrews to thrive in diverse conditions; for instance, their dense provides insulation against cold temperatures in temperate and regions. In semi-aquatic species like the water shrew (Sorex palustris), webbed hind feet fringed with stiff hairs facilitate and in streams and marshy areas. These adaptations allow water shrews to exploit streamside habitats with and vegetation. A few shrew species demonstrate tolerance for human-modified landscapes; for example, the house shrew (Suncus murinus) can inhabit gardens, buildings, and orchards, adapting to fragmented habitats near human settlements. Seasonally, shrews shift to more sheltered microhabitats in winter, such as burrows under logs or tunnels in temperate zones, which offer from frost and wind while allowing continued activity. Species like the least shrew (Cryptotis parvus) utilize cover for protection, remaining active year-round in these subnivean spaces.

Behavior and Ecology

Diet and Foraging

Shrews exhibit an omnivorous diet dominated by , which typically comprise the majority of their intake, including such as and larvae, , spiders, and other arthropods. Occasional consumption of small vertebrates like amphibians or carrion, as well as plant matter such as seeds and fungi, supplements this primarily insectivorous regimen, allowing adaptability to available resources. Due to their elevated basal metabolic rate—reaching approximately 2.5 to 3.5 times that expected for comparably sized mammals—shrews must consume 1 to 2 times their body weight in food daily to sustain energy demands. This voracious appetite stems from their high caloric needs, with species like the common shrew (Sorex araneus) ingesting approximately 80-90% of their body mass per day in wet food, much of which is water-rich invertebrates. Failure to meet this intake can lead to starvation within hours, underscoring their physiological constraints. Shrews are active hunters that rely on acute senses of smell and touch, facilitated by vibrissae (whiskers), to detect and pursue prey in leaf litter, , or undergrowth. Some , such as the short-tailed shrew (Blarina brevicauda), employ venomous saliva to immobilize larger or small vertebrates, enhancing capture efficiency, while others cache excess prey in burrow chambers for later consumption. This approach emphasizes rapid, opportunistic predation over passive waiting. Specialist species like the masked shrew (Sorex cinereus) focus intensely on , preying on caterpillars, grubs, slugs, and spiders using cover for ambush tactics. Shrews do not hibernate but enter daily during periods of food scarcity or cold, reducing metabolic activity to conserve without prolonged . This state allows brief physiological slowdowns, enabling survival when invertebrate availability declines.

Social Structure and Activity Patterns

Shrews exhibit a predominantly solitary , with individuals maintaining exclusive territories to minimize competition for resources. In species such as the short-tailed shrew (Blarina brevicauda), residents occupy small, stationary home ranges at high prey densities and larger, more variable areas at low densities, with minimal overlap between same-sex individuals during the breeding season. Males typically defend larger territories than females, using to mark boundaries and deter intruders, as observed in the lesser (Crocidura suaveolens), where males perform more frequent scent marking and display heightened . This territoriality extends to the (Suncus etruscus), which remains solitary outside of breeding periods, relying on scent markings to enforce spatial separation. Adult interactions are characterized by aggression rather than cooperation, with encounters often escalating to chases, attacks, or vocal threats when territories are breached. In the lesser white-toothed shrew, males are equally aggressive toward both sexes, while females rarely attack other females, indicating sex-specific patterns in agonistic behavior. The Etruscan shrew similarly engages in violent confrontations or avoidance with unfamiliar individuals, underscoring the minimal social tolerance among adults. Cooperative behaviors are largely absent except during maternal care, where females provision and protect litters without male involvement. A notable exception to occurs in maternal-offspring dynamics, exemplified by the "caravanning" behavior in species like the (Suncus murinus). Young follow the mother in a single-file line, maintaining contact through tactile and olfactory cues rather than physical grasping, which facilitates group movement while relying on the mother's scent trails for . This behavior aids in relocating nests or sites, leveraging the young's developing to stay connected. Activity patterns in shrews are largely nocturnal or crepuscular, adapted to their high metabolic rates that necessitate near-continuous foraging. Species such as the forest shrew (Myosorex varius) and greater red musk shrew (Crocidura flavescens) display predominantly nocturnal activity under natural light cycles, with polyphasic rhythms involving multiple short bouts distributed across the 24-hour period. Due to their elevated metabolism, shrews like the common shrew (Sorex araneus) alternate between foraging episodes of approximately 55 minutes and brief rest periods of about 64 minutes, preventing extended sleep to sustain energy demands. The Etruscan shrew exemplifies this with evenly spaced activity bursts, enabling efficient prey capture in low-light conditions. Seasonal variations influence activity levels, with heightened and movement during seasons to support and establishment. In the , spring adults exhibit peak energy expenditure and activity for growth and mating, while summer juveniles maintain high mobility. Winter subadults reduce running and overall activity, increasing rest and targeted to cope with scarcer , resulting in lower absolute energy costs through body size reduction. In response to fluctuating availability, some undertake local movements or dispersal rather than long-distance , as seen in Merriam's shrew (Sorex merriami), which shifts habitats seasonally within limited ranges.

Echolocation and Communication

Shrews in certain genera, such as Blarina and Cryptotis, employ echolocation through the production of ultrasonic clicks to navigate dark environments like underground tunnels. These clicks, generated vocally rather than by tongue snapping as once hypothesized, typically range from 25 to 60 kHz in frequency and serve primarily for obstacle detection and spatial orientation rather than locating prey during hunting. For instance, the northern short-tailed shrew (Blarina brevicauda) emits these broadband, multi-harmonic pulses at rates that increase in novel or cluttered settings, allowing it to interpret echoes for pathfinding. Recent research since 2020 has extended evidence of this ability to additional New World species, including further confirmation in Blarina and related taxa, highlighting convergent adaptations in their auditory systems. A 2024 comparative genomics study revealed genomic adaptations in shrews linked to echolocation, nervous system development, and metabolism. Beyond echolocation, shrews rely on chemical signals for territory maintenance and social signaling, primarily through scent marking with and . These marks convey individual identity and reproductive status, deposited via rubbing behaviors on substrates within home ranges, as observed in species like the musk shrew (Suncus murinus). Ultrasonic vocalizations also play a key role in non-echolocative communication; high-pitched twittering calls, often in the 4-16 kHz range with ultrasonic harmonics, are emitted during distress to signal alarm or during to attract partners. In Suncus murinus, for example, male calls evolve from juvenile vocalizations and incorporate ultrasonic components to facilitate pair . Shrews possess specialized hearing adaptations, including relatively enlarged cavities and cochleae tuned to high frequencies, enabling detection of subtle prey movements such as insect rustling or predator footsteps. This acute sensitivity to sounds above 20 kHz supports both and anti-predator responses across species. However, echolocation is not universal among shrews; it is absent in many taxa like most Sorex species, and their poor vision limits reliance on visual cues, emphasizing acoustic and olfactory modalities instead.

Reproduction and Life Cycle

Mating and Gestation

Shrews generally exhibit a , in which larger males compete aggressively for access to multiple females, as suggested by sexual size dimorphism in species such as the (Suncus murinus). In many soricid species, particularly the musk shrew (Suncus murinus), is induced reflexively by copulation, with the mating stimulus activating neurons in the to trigger release and subsequent follicular maturation within hours. Breeding patterns vary with and . Tropical , like the , breed year-round with peaks in spring and summer, enabling high reproductive output. In contrast, temperate species such as northern shrews breed seasonally from to , producing 1 to 4 litters per year to align with favorable conditions. periods range from 17 to 32 days across , tending to be shorter in smaller-bodied shrews to support their high metabolic rates. Females often overlap reproductive phases by conceiving a new litter while lactating for the previous one, as observed in the (Crocidura russula monacha), where demands partially overlap rather than additively increase, facilitating accelerated breeding cycles. Litter sizes typically vary from 2 to 10 young, depending on the , body size, and resource availability; for example, northern shrews average 4 to 7, while the produces 4 to 8 per litter.

Development and Lifespan

Shrew newborns are altricial, born blind, hairless, and highly dependent on their mother for warmth, nourishment, and protection. At birth, they typically weigh between 0.2 and 0.4 grams and measure about 2 cm in length, though this varies slightly by ; for example, masked shrew (Sorex cinereus) neonates weigh 0.2–0.3 g, while pygmy shrews (Sorex pygmaeus) are around 0.25 g. These tiny, pink, wrinkled young remain in the nest, nursing from the mother for the first 20–30 days, during which they grow rapidly due to their elevated metabolic rates—often tripling or quadrupling their within two weeks. Maternal care is intensive, with the mother providing milk rich in fats and proteins to support this accelerated development, and she may employ behaviors like caravanning to relocate the litter safely. Postnatal growth is exceptionally fast, driven by the shrew's high , which is among the highest of any relative to body size. Young shrews open their eyes and ears around 10–14 days and begin exploring the nest by 20 days, reaching near-adult size in 1–2 months for many species, such as the ( brevicauda), though full body mass may take up to 4 months in some cases. occurs between 20 and 30 days, marking a transition to independence; juveniles must quickly learn to independently to meet their high demands. is achieved rapidly, typically at 1–3 months of age—females often as early as 6 weeks in species like the , and males by 2–3 months—allowing for multiple breeding cycles within their short lives. In the wild, shrew lifespans are brief, averaging 12–30 months, with most individuals rarely surviving beyond 2 years due to intense predation, environmental stressors, and their voracious metabolism. For instance, the common shrew (Sorex araneus) seldom exceeds 14–16 months in natural settings, as adults must consume 200–300% of their body weight daily in food, leading to starvation if inactive for more than 3–4 hours. In captivity, with controlled conditions and ample food, lifespans can extend to 3–4 years, as observed in some common shrew specimens. Juvenile mortality is particularly high, with 50–80% of young dying in the first month from predation, exposure, or failure to learn foraging skills, though rates vary by species and habitat; for the arctic shrew (Sorex arcticus), about 50% perish during this vulnerable period. Overall, these factors contribute to high population turnover, ensuring that only a fraction of shrews reach adulthood.

Taxonomy and Evolution

Classification and Diversity

Shrews are classified in the family Soricidae, which belongs to the mammalian order , a group that also includes moles, hedgehogs, and solenodons. As of 2025, the family comprises approximately 400 species distributed across 27 genera, making it one of the most diverse families of mammals. This diversity reflects their adaptability to various habitats, though all are small, insectivorous mammals characterized by a pointed and rapid . Recent discoveries, including the 2025 description of Nagasorex, continue to expand shrew diversity. The family Soricidae is divided into three main subfamilies based on dental and morphological traits. The Crocidurinae, or white-toothed shrews, is the largest subfamily with 234 species in 9 genera, distinguished by unpigmented teeth lacking the red tint seen in other groups. The Soricinae, known as red-toothed shrews due to iron deposits in their teeth that provide a reddish hue and resistance to wear, includes 158 species across 13 genera. The Myosoricinae, specialized African shrews, encompasses approximately 20 species in 3 genera, often adapted to tropical forest environments with unique ecological roles. Among the genera, Crocidura stands out as the most species-rich and cosmopolitan, with approximately 192 found across , , and , representing a significant portion of the family's diversity. In contrast, Sorex is a key genus in the Holarctic , comprising approximately 86 primarily in the northern temperate zones of and , where it dominates local shrew communities. True shrews of the Soricidae must be distinguished from superficially similar but unrelated mammals bearing the name "shrew," such as elephant shrews (order Macroscelidea), which are more closely related to and , and treeshrews (order Scandentia), which are primitive allied with colugos. These distinctions arise from phylogenetic analyses confirming separate evolutionary lineages, with true shrews uniquely placed within . Recent taxonomic updates have further expanded shrew diversity; in 2025, the new genus Nagasorex was described based on a specimen from in northeastern (Southeast Asia border region), tentatively assigned to the subfamily Myosoricinae due to its 34 teeth—a unique count among shrews—and highlighting ongoing discoveries in understudied areas.

Fossil Record and Evolutionary History

The fossil record of shrews (family Soricidae) extends from the Middle Eocene epoch, approximately 50 million years ago (Ma), to the present day, with the earliest known fossils discovered in and . The oldest records include the genus Domnina from the Middle Eocene of , , dating to around 47 Ma, and Soricolestes from contemporaneous deposits in , consisting primarily of isolated jaws and teeth that highlight early dental specializations for insectivory. Subsequent fossils from the late Eocene and in , such as those of heterosoricids, indicate a gradual diversification across Laurasian continents, though the record remains fragmentary with few complete crania until the . Shrews belong to the order , deriving from early insectivoran-grade mammals that survived the Cretaceous- extinction event around 66 Ma. Within , Soricidae represents the sister group to (moles), with their divergence estimated between 64 and 41 Ma during the Eocene, following an earlier split from (hedgehogs and gymnures) near the Cretaceous- boundary. This lineage likely originated in , where the earliest soricids like Domnina and heterosoricids appear outside the crown group, adapting post-Cretaceous ecosystems through enhanced mechanics, including a double and elongated basicranium, which optimized their insectivorous diet by improving bite force and prey manipulation. A major radiation occurred during the epoch (approximately 23–5 Ma), coinciding with climatic warming and habitat expansion, leading to the diversification of key subfamilies such as Crocidurinae. For instance, the genus Crocidura—now the most speciose mammalian genus—began its proliferation around 19–10 Ma, with early fossils from at ~14 Ma evidencing rapid driven by ecological opportunities in forested and environments. This period also saw the establishment of distinct red-toothed (Soricinae) and white-toothed (Crocidurinae) lineages, adapting to varied prey across and . Several extinct lineages related to shrews underscore their evolutionary breadth within . The Nesophontidae, or island-shrews, comprising genera like Nesophontes, diverged from solenodons around 57 Ma (range 44–69 Ma) and evolved in isolation on the from the middle (~40 Ma), developing shrew-like insectivorous traits such as nocturnal burrowing. These taxa went extinct shortly after colonization in the late , likely due to introduced predators like rats and mongooses, with the last records from in the 1930s. Molecular phylogenetic studies, integrating mitochondrial and nuclear DNA, robustly confirm the of Soricidae, supporting two primary subfamilies (Soricinae and Crocidurinae) and resolving intergeneric relationships that align with calibrations. Additionally, evolution has occurred independently in multiple shrew lineages, including genera such as , Neomys, and Crocidura, through the co-option of salivary proteins like kallikrein-1 serine proteases, enhancing prey immobilization and aiding diversification in competitive niches. This convergent trait, seen across at least four eulipotyphlan events, parallels adaptations in distantly related venomous mammals.

Human Interactions and Conservation

Relationship with Humans

Shrews play a beneficial ecological role in human-managed landscapes by preying on insect populations, thereby aiding natural pest control in gardens and farms. For instance, the northern short-tailed shrew (Blarina brevicauda) consumes large quantities of invertebrates, including crop pests such as the larch sawfly, helping to reduce damage to agricultural areas. Similarly, various shrew species contribute to invertebrate control, which supports farmers by limiting pest outbreaks without relying solely on chemical interventions. However, shrews can occasionally cause minor crop damage through seed consumption. Some species, including the , incorporate and roots into their , potentially affecting planted or broadcast in agricultural settings, though this impact is generally limited compared to their predatory benefits. Reports from gardeners indicate shrews may eat potatoes in the field, leading to localized losses. In certain regions, shrews are considered pests due to their proximity to human habitation and potential to spread diseases. The Asian house shrew (Suncus murinus), native to South and Southeast Asia, frequently invades homes and urban areas, achieving high population densities in household environments. These shrews serve as reservoirs for pathogens, including Leptospira species that cause leptospirosis, a zoonotic disease transmitted through contact with their urine-contaminated environments; studies in endemic areas like Indonesia have detected high infection rates in this species. Culturally, the term "shrew" has been used in European literature and folklore to denote an ill-tempered or scolding person, a metaphor popularized by William Shakespeare's play The Taming of the Shrew (c. 1590–1592), which draws on earlier folk traditions of taming unruly women. The play adapts motifs from European folktales, such as Danish stories involving shrew-taming, embedding the animal's name as a symbol of discord in Western cultural narratives. In some European folklore, shrews were viewed as omens of misfortune, reflecting superstitions about their secretive, nocturnal habits. Shrews are valuable model organisms in scientific research, particularly for studies on high metabolism and venom systems. Their exceptionally elevated basal metabolic rates—often several times higher than predicted for mammals of similar size—make species like the common shrew (Sorex araneus) and least shrew (Cryptotis parva) ideal for investigating energy demands, thermoregulation, and adaptive responses to environmental stress, such as seasonal brain size changes linked to metabolic efficiency. Additionally, venomous shrews, including the northern short-tailed shrew, are studied for their oral venom compositions, which include proteins causing rapid paralysis and analgesia in prey, providing insights into mammalian toxin evolution and potential biomedical applications. Shrews have not been domesticated for human use and are rarely involved in the pet trade, owing to their demanding care requirements, including constant feeding to sustain their rapid and short lifespans typically under two years. While some species like the Japanese shrew (Crocidura dsinezumi) have been bred in settings after capture and generational adaptation, they are not suited for companionship due to their wild behaviors and specialized needs.

Threats and Conservation Status

Shrews face numerous threats that impact their populations worldwide, primarily driven by human activities and environmental changes. through , agricultural expansion, and urbanization fragments their preferred moist, vegetated environments, reducing available shelter and foraging areas. For instance, in , the (Sorex ornatus relictus) has experienced severe habitat loss from agricultural development and water diversion, contributing to its endangered status. exacerbates these issues by altering precipitation patterns and temperatures, which disrupts prey availability—shrews' primary food source—leading to population declines in affected regions. Additionally, the widespread use of pesticides diminishes populations, indirectly starving shrews and posing direct toxicity risks through in their . Predation and competition from further compound these pressures, particularly on islands and in altered ecosystems. Invasive predators such as the (Neovison vison) have been documented preying on native shrews, including the Iberian water shrew (Neomys anomalus), in waterways, accelerating local declines. Similarly, introduced rats and fish have contributed to the of the Christmas Island shrew (Crocidura trichura), Australia's only native shrew species, declared extinct in 2025 due to and invasive impacts. These non-native species outcompete shrews for resources and increase mortality rates, highlighting the vulnerability of insular populations. According to the , a significant number of shrew are threatened with , with several classified as Endangered or Vulnerable due to these cumulative threats. The (Galemys pyrenaicus), a semi-aquatic relative closely allied with shrews, is listed as Endangered, primarily from , dam construction, and in its Iberian range, which have caused up to 50% population declines since 2011. Conservation efforts include establishing protected areas across and to safeguard critical habitats, such as riparian zones and forests, and implementing monitoring programs to track impacts and population trends. For example, in , recovery strategies for the Pacific water shrew (Sorex bendirii) emphasize habitat restoration and invasive control to mitigate ongoing risks. However, major reintroduction programs remain limited due to shrews' short lifespans and high metabolic demands. Despite these initiatives, substantial gaps persist in shrew conservation knowledge, particularly in tropical regions where many species remain understudied amid accelerating . In the and Mexican volcanic belts, limited data on population fluctuations and habitat responses hinder effective protection, leaving tropical shrews exposed to emerging threats like intensified and agricultural conversion in the 2020s. Enhanced research and transboundary monitoring are essential to address these deficiencies and prevent further extinctions.

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