Fact-checked by Grok 2 weeks ago

Juniper titmouse

The Juniper titmouse (Baeolophus ridgwayi) is a small, plain gray in the Paridae, measuring about 5¾ inches (15 cm) in length, with a short on its head, a prominent , rounded wings, and a square-tipped tail. It was recognized as a distinct in 1996 after being split from the (formerly combined as the plain titmouse) due to differences in , vocalizations, genetics, and habitat preferences. This non-migratory is a year-round resident in warm, dry pinyon-juniper woodlands, as well as or pine- forests, and occasionally riverine or areas with shade trees, primarily across the interior , including , the , the Southwest, and parts of . It forages acrobatically in trees and shrubs, often hanging upside down to glean like caterpillars and , spiders, , pinyon nuts, acorns, berries, and small fruits, while also storing for winter and visiting feeders for sunflower and . Its vocalizations include harsh, scratchy calls such as "see-dee-dee," and it flies with a direct, undulating pattern. Breeding occurs from to May, with pairs nesting in natural tree cavities or nest boxes, where the female lays 5–6 white eggs speckled with reddish-brown spots and incubates them for 14–16 days; both parents feed the young, which after 16–21 days. The species is classified as Least Concern by the IUCN, with stable populations and no major threats identified, though its habitat-dependent nature makes it sensitive to woodland alterations; the oldest recorded individual lived over 4 years.

Taxonomy

Etymology

The common name "Juniper titmouse" reflects the bird's strong association with pinyon-juniper woodlands, where it primarily resides and forages; this designation was adopted following the taxonomic split from the plain titmouse (now including the ), to highlight distinct habitat preferences. The term "titmouse" is a longstanding English name for small, acrobatic songbirds in the family Paridae, derived from "titemose," combining "tit" (a for something small) and "mose" or "mase" (from "māse," denoting a small or tit). This etymology underscores the bird's diminutive size and woodland habits, with historical usage dating back to at least the for similar . The scientific binomial Baeolophus ridgwayi originates from the genus Baeolophus, coined in 1850 by German ornithologist Jean Cabanis from the Greek words "baiós" (small) and "lóphos" (crest), alluding to the species' subtle head crest. The specific epithet "ridgwayi" honors American ornithologist Robert Ridgway (1850–1929), a pioneering systematist who first described the subspecies as Lophophanes inornatus griseus in 1882 based on specimens from the Great Basin. The name Baeolophus ridgwayi was formalized in 1902 when Charles Wallace Richmond renamed the subspecies Parus inornatus ridgwayi in the Proceedings of the Biological Society of Washington, replacing the preoccupied epithet "griseus" (meaning gray) due to nomenclatural conflicts under the emerging . This renaming exemplified early 20th-century practices in avian taxonomy, where junior synonyms were often resolved by honoring influential figures like Ridgway, who contributed extensively to North American bird classifications through works such as the of North American Birds.

Classification history

The subspecies was first described by Robert Ridgway in 1882 as Lophophanes inornatus griseus, based on specimens from Iron City, Utah (in the ). In 1902, Charles Wallace Richmond provided the replacement name Parus inornatus ridgwayi due to the preoccupied "griseus". For much of the , it was classified as part of the widespread plain titmouse ( inornatus) complex due to their nearly identical plumage and overall morphology, which made differentiation challenging without detailed examination of geographic variation. In 1996, comprehensive research by Carla Cicero demonstrated significant differences between the interior and coastal populations of the plain titmouse, including distinct vocalizations, habitat preferences, and genetic lineages revealed through molecular analyses such as allozyme electrophoresis and sequencing. These findings indicated that the interior form, previously P. i. ridgwayi, represented a separate species adapted to pinyon-juniper woodlands. As a result, the American Ornithologists' Union (AOU) formally split the plain titmouse in its checklist supplement, recognizing the Juniper titmouse as Baeolophus ridgwayi and the coastal form as the (B. inornatus), while also transferring both from the Eurasian-centered genus to to better reflect their phylogenetic affinity with other North American titmice. The full taxonomic placement of the Juniper titmouse is Kingdom Animalia, Phylum Chordata, Class Aves, Order Passeriformes, Family Paridae, Genus , Species ridgwayi. Subsequent molecular studies, including cytochrome-b sequencing, have reinforced the distinct lineages of B. ridgwayi and B. inornatus, dating their divergence to the late Pleistocene-Holocene transition around 12,000 years ago. This classification has been upheld without further revisions in the (AOS, successor to AOU) checklists and the International Ornithological Congress (IOC) World Bird List as of 2025, confirming the species' in modern avian .

Subspecies

The Juniper titmouse (Baeolophus ridgwayi) is currently recognized as comprising two subspecies, distinguished primarily by geographic distribution, morphology, vocalizations, and genetics. The nominal subspecies, B. r. ridgwayi (Richmond, 1902), occupies the majority of the species' range across the Great Basin and extends from southeastern Oregon southward through Idaho, Nevada, Utah, Arizona, New Mexico, and into northeastern Mexico. In contrast, B. r. zaleptus (Oberholser, 1932) is more restricted, occurring in the western portion of the range, particularly the Inyo-White Mountains region and adjacent high-elevation pinyon-juniper woodlands in southeastern Oregon, eastern California, and western Nevada. The B. r. ridgwayi tends to exhibit a larger , with adults weighing up to 22 g, and slightly darker gray overall. This form is adapted to a broader array of arid and semi-arid habitats within its extensive . The B. r. zaleptus is generally smaller, with weights ranging from 10–15 g, and features paler that may reflect s to the more extreme arid conditions of its limited high-elevation range. These are delimited based on consistent morphological differences (such as and coloration), distinct vocal repertoires, and genetic markers, with no documented hybridization between them despite adjacent ranges. Such intraspecific variation underscores the ' adaptation to diverse environmental gradients in western North American woodlands.

Description

Physical characteristics

The Juniper titmouse (Baeolophus ridgwayi) is a small measuring approximately 14–15 cm (5.5–5.9 in) in length, with a of approximately 23 cm (9.1 in) and a body mass ranging from 10–22 g. It possesses a long, slender body, short neck, and medium-length tail, contributing to a compact yet elongated ; the head appears pointed due to a short, conspicuous of feathers. Its plumage is uniformly plain gray, with the upperparts medium to dark gray and the underparts paler gray, sometimes with a faint olive-brown tinge on the lower flanks; there is no in coloration or size. The large, contrasts sharply against the unmarked gray face, enhancing its alert expression, while and back appear slightly darker than the rest of the body. Juveniles exhibit similar but with duller, more filamentous body feathers (particularly on the undertail coverts) due to reduced barb density, paler upperwing coverts, and a less defined . Key identifying features include a short, thick, dark bill that is rounded and stout, adapted for cracking , and strong legs and feet that enable acrobatic postures during . The is more prominent and pointed than in related species like chickadees, which lack a crest entirely. Compared to the closely related (Baeolophus inornatus), the Juniper titmouse has a cooler, grayer overall tone rather than the warmer brownish-gray of the Oak titmouse, along with a slightly longer bill (averaging 13.5 mm versus 12.7 mm). Unlike the (Poecile atricapillus), it lacks bold black-and-white facial markings or a distinct cap.

Vocalizations

The song of the Juniper titmouse consists of a medium-pitched (1–4 kHz), rolling series of 5–15 syllables delivered in 1–2 seconds, often featuring alternating high and low frequencies or rapid trills that give it a snappier quality compared to the harsher song of the closely related . Males primarily produce this song for territory defense and advertisement, typically from exposed perches, with singing peaking in mid-winter through spring and most intense in the mornings. Individual males possess repertoires of 1.6–13.6 song types, showing some regional variation in complexity but maintaining a distinct, rapid-fire delivery overall. The species produces a variety of calls, including the harsh "tsicka dee," comprising 1–7 high-pitched notes (6–8 kHz) followed by lower chattering, used for alarm and territorial purposes. Alarm and situations also elicit fast, harsh chatter calls, while high-pitched (7–9 kHz) "see" whistles serve as alerts, and soft lisping "sip" notes function during foraging or nest care. Incubating females emit a loud, snake-like hiss when disturbed to deter predators, and rare calls (sit-sit-sit) occur in contexts of sexual excitement. Juniper titmice vocalize year-round, with calls maintaining steady use outside the breeding peak, and pairs often duet during breeding, where the female contributes calls to the male's song. Juveniles beg with high-pitched (7–10 kHz) twitter peeps, though song learning remains unstudied in detail. Recordings of these vocalizations, including songs and calls in the 4–8 kHz range, are extensively documented in the Cornell Lab of Ornithology's Macaulay Library, aiding in auditory identification.

Distribution and habitat

Geographic range

The Juniper titmouse (Baeolophus ridgwayi) is a year-round resident in western , distributed from southeastern and southwestern southward through , , southwestern , central and south-central , southeastern , central and southern , southern , extreme western , and into northeastern , . This range encompasses the and Upper Sonoran life zones, with the eastern limit extending to the western in via isolated populations in the Mountains; no trans-Mexican populations occur beyond northeastern . The is non-migratory, with sedentary pairs defending year-round territories; rare appear outside the core range, such as occasional sightings in . The distribution has remained stable since the 1996 taxonomic split from the oak titmouse, with no significant range expansions or contractions documented as of 2025.

Habitat requirements

The Juniper titmouse (Baeolophus ridgwayi) is a habitat specialist adapted to dry, open woodlands in arid to semi-arid climates of the . It primarily occupies pinyon-juniper woodlands dominated by species such as single-leaf pinyon (), Colorado pinyon (), Utah juniper (), and western juniper (), where these trees form a sparse canopy suitable for . These habitats often include understories of sagebrush () or Joshua trees (), providing additional cover, while single-species juniper stands or mixed configurations with oaks (Quercus spp.) occur in some regions. Elevation preferences range from approximately 2,250 to 8,000 feet (686–2,438 m), typically on - and west-facing slopes in mid-elevation with open spacing and rocky understories. The requires mature or senescent —often with diameters at breast height of 6–20 inches and in stands with at least 35% canopy cover and ≥37 senescent per —for natural cavities or woodpecker-excavated holes used in nesting and roosting. Microhabitat features include dense foliage clusters for overnight roosting and protection, with secondary use of desert riparian areas featuring willows or cottonwoods, though it avoids dense forests and urbanized landscapes lacking these woodland elements. Following its taxonomic split from the (B. inornatus) by the American Ornithologists' Union in 1996—based on genetic, vocal, and ecological distinctions—the juniper titmouse has been recognized as a specialist in juniper-pinyon ecosystems, contrasting with the oak titmouse's affinity for -dominated woodlands. This specialization underscores its dependence on late-successional pinyon-juniper stands for survival, with populations declining in areas where such mature habitats are fragmented.

Behavior and ecology

Social structure

The Juniper titmouse exhibits a monogamous , with pairs forming strong, typically lifelong bonds early in the first year and maintaining them year-round unless one partner dies. These pairs defend all-purpose territories averaging 1.2–1.3 (3 acres), which encompass , nesting, and roosting areas, through vocalizations and displays such as crest-raising and harsh calls directed at intruders.103[0361:FIPTIT]2.0.CO;2) Throughout most of the year, Juniper titmice are observed as solitary individuals or stable pairs, but following the breeding season, they form small family groups consisting of 3–8 birds, including parents and fledglings, which remain cohesive into the fall. These family units do not typically merge with other conspecific groups, and large intraspecific flocks are rare. However, during the nonbreeding period, particularly in fall and winter, they may join mixed-species foraging flocks with bushtits (Psaltriparus minimus), ruby-crowned kinglets (Corthylio calendula), and various warblers, particularly when food is scarce, enhancing social dynamics without forming permanent associations. No has been documented in this species. Social interactions among Juniper titmice involve territorial antagonism, including song exchanges, scolding calls, wing quivering, and pursuit flights to repel rivals, with both sexes participating aggressively in . At nests, females display bold defensive , such as hissing like a snake when disturbed by potential threats. Pairs and family groups show curiosity toward human observers in some contexts but prioritize evasion or vocal warnings over direct confrontation outside of or nest . For roosting, Juniper titmice select sheltered sites such as natural tree cavities, dense foliage, or occasionally artificial birdhouses, with individuals or pairs using these locations year-round to conserve . Females may roost in prospective nest cavities up to a month before egg-laying, and in cold weather, they huddle closely for warmth, though specific huddling patterns remain understudied.

Foraging and diet

The Juniper titmouse maintains an omnivorous diet that varies seasonally, reflecting changes in food availability within its pinyon-juniper woodland habitat. In spring and summer during the breeding season, arthropods dominate the intake, with such as , caterpillars, flies, leafhoppers, , and wasps, along with spiders, comprising the majority of consumed items to support high energy demands for and nestling . Plant material, including berries and seeds, remains a supplementary component year-round but increases notably in fall and winter, when large seeds from , juniper berries, acorns, and other seeds become primary foods. Foraging occurs primarily through gleaning techniques on foliage, twigs, branches, trunks, and occasionally the ground, with the displaying acrobatic by hanging upside down or headfirst to access hidden prey. It employs its strong to probe crevices, chip at surfaces, and hammer tough seeds or nuts against branches to crack them open, while using its legs to hold larger items in place. Seeds are frequently cached in fissures or other sheltered spots for winter retrieval, aiding survival during periods of scarcity. Juniper titmice spend much of their time in the canopy or on woody substrates, occasionally hovering briefly or pursuing mid-air, though such aerial captures are infrequent. They readily exploit food sources by visiting feeders for sunflower seeds, , and , particularly in winter near suitable and tree cover.

Reproduction

Breeding biology

The Juniper titmouse (Baeolophus ridgwayi) breeds primarily from early to , with egg-laying occurring from mid-March to late May and fledglings observed as late as ; this timing aligns with increasing photoperiod and seasonal availability that supports nestling provisioning. Pairs are typically monogamous, forming bonds in their first year and remaining together for life while defending year-round territories. The female lays a of 4–7 eggs, averaging 5.5 (range typically 4–7, mode 6), once per season and rarely twice; the eggs are white, short subelliptical to elliptical in shape, and may bear faint reddish-brown speckles. Incubation lasts 14–16 days and is performed solely by the female, who develops a single ventral brood patch; during this period, the male feeds the incubating female. Nestlings hatch altricial, blind, and helpless, and are brooded by the female while both parents feed them and remove fecal sacs; the nestling period spans 16–21 days, after which the young simultaneously, capable of short flights. Post-fledging, both parents continue to feed the juveniles for about one month, during which gradually disperse and young begin foraging independently by around five weeks of age, achieving full independence by August. Breeding success is limited primarily by predation on eggs and nestlings, with key predators including Woodhouse’s scrub-jays and , though specific fledging rates remain undocumented for this species.

Nesting habits

The Juniper titmouse is a secondary cavity nester, primarily using natural cavities in dead snags or live trees, old holes, or artificial nest boxes. These sites are typically located 1–4.4 m (3.6–14.4 ft) above ground, with a median height of about 3.2 m (10.5 ft), often in , , or trees. Nest construction is carried out almost exclusively by the over 4–10 days, forming a cup-shaped structure from grass, shredded bark, moss, rootlets, straw, feathers, and hair, with the inner lining softened by or for the eggs. During the and early nestling periods, the broods the eggs and young, often hissing defensively if disturbed, while the guards the and makes more frequent visits to the nest, delivering food to support her. Both parents then feed the altricial nestlings, prioritizing in their diet (as detailed in the foraging and diet section). If a nesting attempt fails, pairs may re-nest and attempt a second in a new cavity site.

Conservation

Population status

The global breeding population of the Juniper titmouse (Baeolophus ridgwayi) is estimated at 180,000 individuals, with approximately 99% occurring in the United States and 1% in . More recent assessments by Partners in Flight place the total number of mature individuals at 6,500,000, reflecting updated monitoring data. Population trends indicate stability across the species' range from 1966 to 2015, based on data from the North American Breeding Bird Survey. Subsequent analyses show an increasing trend, particularly in the region, with an estimated annual growth of 11.7% from 2001 to 2011. The International Union for Conservation of Nature (IUCN) classifies the Juniper titmouse as Least Concern, with the 2025 assessment noting no immediate but emphasizing the need for continued due to its dependence on specific habitats. Breeding densities in optimal piñon-juniper woodlands typically range from 0.1 to 0.5 pairs per (equivalent to roughly 4–20 pairs per 100 acres), with higher densities observed in core areas where habitat conditions are favorable. The species exhibits relatively low population densities compared to its close relative, the , likely due to the patchier distribution of suitable juniper-dominated habitats. The oldest recorded banded Juniper titmouse—a female recaptured in —lived at least 4 years and 2 months. These estimates are derived from banding recoveries and survivorship studies, highlighting the species' vulnerability to annual mortality factors despite stable overall populations.

Threats and management

The primary threats to the Juniper titmouse stem from habitat loss and in pinyon-juniper woodlands, including logging for fuelwood, fence posts, and Christmas trees, as well as and historical practices to expand livestock grazing areas. suppression has promoted the encroachment of young junipers, leading to denser stands that reduce the open woodland structure preferred by the for foraging and nesting. exacerbates these issues by drying out woodlands and causing decline through prolonged droughts and warmer temperatures, which diminish key food sources like pine nuts. However, the faces lower overall human impacts compared to the closely related , owing to its occurrence in sparsely populated regions with substantial federal land ownership. Secondary threats include nest predation by snakes, scrub-jays, and potentially domestic cats in areas near human development, though the latter is limited by the bird's remote habitat preferences. Conservation management for the Juniper titmouse benefits from protections on national forests and monuments, such as Great Basin National Park, where pinyon-juniper habitats are preserved under multiple-use policies that emphasize retention of mature trees with nesting cavities. Nest box programs in fragmented landscapes, like those implemented by community groups in New Mexico, provide artificial cavities to supplement natural sites and support breeding success. Population monitoring occurs through the North American Breeding Bird Survey, which tracks trends across the species' range. Classified as Least Concern by the IUCN with a stable population, the Juniper titmouse requires no targeted recovery plan at present. Looking ahead, the species remains potentially vulnerable to intensified droughts under ongoing , with research into habitat resilience—such as prioritizing cooler slopes for —continuing as of 2025.

References

  1. [1]
    Juniper Titmouse Overview, All About Birds, Cornell Lab of Ornithology
    The Juniper Titmouse is a plain gray bird with a prominent black eye and a feisty tuft of feathers on its head.
  2. [2]
    Juniper Titmouse | Audubon Field Guide
    A plain grayish bird with a short crest. Very similar to Oak Titmouse, usually a bit grayer (less brownish). Best identified by range, entirely separate except ...Missing: facts | Show results with:facts
  3. [3]
    Titmouse - Etymology, Origin & Meaning
    Originating in early 14c. from Old English "tit" (small) + "mase" (titmouse), from Proto-Germanic *maison meaning "little, tiny," titmouse denotes a small, ...
  4. [4]
    TITMOUSE Definition & Meaning - Merriam-Webster
    Word History. Etymology. Middle English titemose, tetmose "tit (European bird of the family Paridae)," from tite-, tet ...
  5. [5]
    tufted titmouse - Baeolophus bicolor (Linnaeus) - PlantSystematics.org
    Jan 29, 2009 · Baeolophus is composed of two Greek words, baios, "little" and lophos, "crest" alluding to the crest on the head. The species epithet, bicolor, ...Missing: etymology | Show results with:etymology
  6. [6]
    Systematics - Juniper Titmouse - Baeolophus ridgwayi
    Feb 6, 2017 · Close ). Note that the original name for this species was Lophophanes inornatus griseus Ridgway, 1882, but because Richmond supplied a ...
  7. [7]
    Baeolophus ridgwayi (Juniper Titmouse) - Avibase
    Baeolophus ridgwayi. Original description. Citation: (Richmond, CW 1902). Reference: Proc. Biol. Soc. Washington 15 p.155. Protonym: Parus inornatus ridgwayi.Missing: first | Show results with:first
  8. [8]
    AOU Check-list Supplement
    1987). p. 516. Parus inornatus, Plain Titmouse, is divided into two species, Baeolophus inornatus (Gambel), Oak. Titmouse, and Baeolophus ridgwayi (Richmond) ...
  9. [9]
    Juniper Titmouse Identification - All About Birds
    The Juniper Titmouse is a small songbird, but the long body, short neck, and medium-long tail makes it appear bigger than it is.
  10. [10]
    Juniper Titmouse - Species Information and Photos
    The two are very similar in appearance, but are separated by geographic range and preferred habitat. The Juniper Titmouse is in drier juniper habitats of the ...Missing: zaleptus differences
  11. [11]
    Plumages, Molts, and Structure - Juniper Titmouse - Birds of the World
    Feb 6, 2017 · Juvenile (First Basic) Plumage ... Present primarily May–August. Similar to Definitive Basic (adult) plumage (see below), but juvenile body ...
  12. [12]
    Juniper Titmouse Life History - All About Birds
    The Juniper Titmouse is a plain gray bird with a prominent black eye and a feisty tuft of feathers on its head. What it lacks in color, it makes up for with ...
  13. [13]
    Titmice at Lava Beds
    With the 7th edition A.O.U. Check-list, however, the "Plain Titmouse" was split into two species: Oak Titmouse Baeolophus inornatus of oak woodlands Oregon to ...
  14. [14]
    Sounds and Vocal Behavior - Juniper Titmouse - Baeolophus ridgwayi
    Calls. The calls of the Juniper Titmouse are highly variable, although detailed study is lacking.
  15. [15]
  16. [16]
    Baeolophus ridgwayi - NatureServe Explorer
    Formerly considered part of B. inornatus, but B. ridgwayi split off by AOU (1997). Renamed B. griseus (griseus was original subspecific epithet given by ...Missing: etymology | Show results with:etymology
  17. [17]
    Habitat - Juniper Titmouse - Baeolophus ridgwayi - Birds of the World
    Like the Oak Titmouse, it frequents warm, arid open woodland (Figure 3), and is most common where juniper is dominant and where large, mature trees are present ...Missing: griseus | Show results with:griseus
  18. [18]
    None
    ### Habitat Details for Juniper Titmouse
  19. [19]
    [PDF] Juniper Titmouse (Baeolophus ridgwayi)
    Juniper Titmouse is a Species Conservation Concern, Level 1 species for New Mexico, with a total assessment score of 19. It receives a high vulnerability score ...
  20. [20]
    Behavior - Juniper Titmouse - Baeolophus ridgwayi
    Actively moves from branch to branch and tree to tree. Prefer to stay close to arboreal cover, flying between trees in shallow undulating motion.Behavior · Self-Maintenance · Social And Interspecific...
  21. [21]
    Breeding - Juniper Titmouse - Baeolophus ridgwayi
    Departure From Nest. Young Oak Titmice leave the nest when capable of climbing to cavity entrance; presumably capable of flying short distances, but do not fly ...Breeding · Nest Site · Microhabitat; Site...
  22. [22]
    Diet and Foraging - Juniper Titmouse - Baeolophus ridgwayi
    Both Juniper and Oak titmice have strong, stout bills and seem to use similar foraging methods. Juniper Titmouse uses its bill to hammer acorns, pinyon nuts, ...Missing: legs | Show results with:legs
  23. [23]
    [PDF] Life history account for Juniper Titmouse
    Former plain titmouse was recently split into the juniper titmouse and the oak titmouse (B. inornatus) and placed in the genus Baeolophus (Cicero 1996, Slikas ...
  24. [24]
    All About Juniper Titmice (Baeolophus ridgwayi) (JUTI) - Sialis.org
    Preferred Nesting Habitat: Warm, dry habitats of open woodland with lots of large junipers or mixed piñon-juniper woodland, especially with dense canopy.
  25. [25]
    [PDF] Lake Powell Pipeline Project - Utah Division of Water Resources
    Apr 30, 2016 · The juniper titmouse prefers warm, dry habitats of open woodland ... re-nesting attempts. Breeding adults generally depart from their ...
  26. [26]
    Juniper Titmouse Baeolophus Ridgwayi Species Factsheet | BirdLife ...
    This species has an extremely large range, and hence does not approach the thresholds for Vulnerable under the range size criterion (Extent of Occurrence ...Missing: etymology | Show results with:etymology<|separator|>
  27. [27]
    JUNIPER TITMOUSE Of Birds and Brush - wieteke holthuijzen
    Apr 8, 2014 · which was recently split from the plain titmouse (Parus inornatus) in 1996 (Cicero 2000, 2004). The juniper titmouse is a small, gray bird ...
  28. [28]
    Longevity Records - Bird Banding Laboratory - USGS.gov
    Previously banded bird trapped and released during banding operations, Alive - Released/Left On Bird. Juniper Titmouse, 4 years 02 months, 06/17/2008, New ...
  29. [29]
    Demography and Populations - Juniper Titmouse - Birds of the World
    Mean territory size of Juniper Titmouse in western Nevada was estimated to be 1.3 ha (Panik 1976 Panik, H. R. (1976). The vertebrate structure of a pinyon ...Missing: bonding | Show results with:bonding
  30. [30]
    Conservation and Management - Juniper Titmouse - Birds of the World
    The primary threats to habitats include the cutting of trees for fuelwood, rangeland conversion, Christmas trees, and fence posts (Schmidt 1994 ...
  31. [31]
    Juniper Titmouse - Oregon Conservation Strategy
    Juniper Titmice use mature juniper trees with cavities for nesting. They require expansive areas of mature juniper habitat, especially in winter.Missing: age | Show results with:age<|separator|>
  32. [32]
    Tackling a (Bird) Housing Shortage - National Wildlife Federation
    Apr 1, 2019 · To provide nesting sites for the juniper titmouse (above), high school students built 70 nest boxes, personalizing each box (below) with their names and other ...Missing: habits | Show results with:habits
  33. [33]
    [PDF] Juniper Titmouse - Baeolophus ridgwayi - b State Species Abstract a
    NATURAL HISTORY. Taxonomy: In 1997, Plain Titmouse (Parus inornatus) was split into two geographically distinct species.