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Turquoise parrot

The Turquoise parrot (Neophema pulchella) is a small, ground-feeding endemic to southeastern , measuring approximately 20 cm in length and weighing 35–46 g. Males are brightly colored with a deep face, bright green upperparts, yellow underparts tinged orange on the breast, underwing coverts, and a distinctive brown or red shoulder patch, while females are duller overall with a paler face, or lores, a pale green breast, and no shoulder markings. Juveniles resemble females but develop more on the face with age. This species belongs to the genus Neophema in the family and is known for its quiet, sociable nature, often foraging in small groups on the ground. The Turquoise parrot inhabits a variety of lowland environments up to 700–1,130 m , including open woodlands, grasslands, heathlands, shrublands, and ecotones between forests and farmlands, particularly those with a grassy and scattered trees. Its distribution spans from southeastern (around 26°S) through eastern to north-central , covering an extent of occurrence of about 771,000 km², though it is largely absent from higher altitudes and more arid inland areas. The population is estimated at around 20,000 mature individuals and appears stable, with some local increases in due to to introduced like cape weed. Behaviorally, the Turquoise parrot is mostly resident and sedentary, though it may form nomadic flocks outside breeding season; it roosts communally in tree hollows and emits soft metallic calls in flight or high-pitched twittering while feeding. Its diet consists primarily of seeds from native and introduced grasses and herbs (such as Leucopogon microphyllus and Stellaria media), supplemented by flowers and fruits. Breeding occurs mainly from August to December, sometimes extending to April–May, with nests in tree hollows or stumps containing 4–6 eggs that hatch after about 18–19 days and fledge at 4–5 weeks. Major threats include predation by introduced foxes and , habitat degradation from and land clearing, loss of hollow-bearing trees for nesting, and inappropriate regimes that reduce grassy areas. Despite these pressures, the species is classified as Least Concern on the due to its stable population and wide distribution, and it is listed under Appendix II for international trade regulation. Conservation efforts focus on protecting remnants and managing threats in agricultural landscapes.

Taxonomy

Classification

The turquoise parrot (Neophema pulchella) belongs to the order Psittaciformes, family , subfamily Platycercinae, and Neophema, which includes other small Australian grass parrots such as the (Neophema splendida). The species was first described by naturalist George Shaw in 1792 under the name Psittacus pulchellus in the Psittacus, based on a specimen likely from the Leverian Museum collection. The current binomial name Neophema pulchella was established when Italian ornithologist Tommaso Salvadori created the Neophema in 1891 to accommodate this and related species, reflecting their distinct morphological and ecological traits within the broad-tailed parrots. Neophema pulchella is considered a monotypic with no recognized , as genetic and morphological variation across its range does not warrant further subdivision. Molecular phylogenetic studies, including analyses of mitochondrial genomes and nuclear loci, place it in a with the , with divergences among Neophema species estimated at approximately 2–3 million years ago during the late .

Naming and etymology

The "turquoise parrot" derives from the vivid turquoise-blue coloration on the male's face and upper breast, a feature that distinguishes it among . This name, along with the variant "turquoisine parrot," emerged in English ornithological shortly after the species' formal description, reflecting early observers' focus on its striking . The scientific name Neophema pulchella combines the Neophema with the specific pulchella. The Neophema, established by Tommaso Salvadori in 1891, originates from the words neo- (new) and phema (voice or sound), implying "new voice" and alluding to the parrots' distinctive calls; it replaced the earlier Euphema established by in 1832, which means "good voice" from eu- (good) and phema. The species name pulchella, a form of the Latin pulcher (beautiful), translates to "little beautiful one," highlighting the bird's attractive appearance; it was first applied in the original as Psittacus pulchellus by George in 1792 in The Naturalist's Miscellany. Historically, the turquoise parrot appeared under synonyms such as Lathamus azureus (coined by René Primevère Lesson in 1830, with azureus from for "sky-blue") before its placement in Neophema by Italian ornithologist Tommaso Salvadori in 1891, which formalized its current nomenclature under emerging international standards. No widely documented Australian names for the have been recorded in historical ornithological sources. Post-20th-century revisions under the (ICZN), adopted in 1961 and updated thereafter, stabilized the name Neophema pulchella by prioritizing Shaw's 1792 description as the valid type, preventing displacement by junior synonyms and ensuring nomenclatural consistency across global avian taxonomy.

Physical description

Morphology and measurements

The (Neophema pulchella) is a small, slender with an average total length of 20–22 cm from the tip of the bill to the end of the tail. Its wing length measures approximately 10.7–11.6 cm, with a of 32 cm, and it weighs 35–45 g on average. Males are slightly heavier, typically 40–45 g, while females average 35–40 g, reflecting minimal sexual size dimorphism. The exhibits a lightly built with a long, graduated tail, aiding in maneuverability. The wings are short and rounded, adapted for agile, undulating flight through open woodlands and grasslands. The is short, curved, and robust, suited for cracking seeds, its primary food source. As with other parrots, the feet are zygodactyl, featuring two toes directed forward and two backward, which supports both perching in trees and on the ground.

Plumage and sexual dimorphism

The turquoise parrot exhibits marked in its , with males displaying more vibrant colors than females. Adult males feature a bright turquoise-blue face and extending to the ear coverts, grading lighter on the cheeks, contrasted against bright upperparts and underparts. A distinctive brick-red to crimson patch on the inner median and lesser secondary coverts of the upperwing is visible primarily in flight, while the wings are edged in with black tips, and the tail shows pale central feathers with rich outer tips and edges. Adult females are duller overall, with a more subdued olive-green to pale blue face restricted to the forehead and cheeks, often featuring a whitish or cream-colored mask around the eyes and lacking the extensive blue of males. Their upperparts and body are a muted yellow-green, with pale green on the breast and a yellow belly sometimes tinged in older individuals; the red wing patches are absent or greatly reduced, replaced by a pale off-white underwing bar, and the tail mirrors the male's pattern but with less intensity. Juveniles resemble females in plumage but are even less vibrant, with pale blue limited to the and cheeks, rudimentary or absent red on the wing coverts, and overall subdued yellow-green tones; they also possess a shorter compared to adults. Both sexes attain immature plumage resembling that of adults through a partial molt within the first six months, though juvenile and feathers are retained until the post-breeding molt around one year of age, achieving full adult coloration early in the second year. The undergoes an annual post-breeding molt commencing around one year of age, typically in late summer following the breeding season, during which replace body feathers and eventually over several weeks.

Distribution and habitat

Geographic range

The turquoise parrot (Neophema pulchella) is native to southeastern , with its current range extending from southeastern near , through the tablelands and slopes of eastern , to northeastern , including around and extending to east . This distribution is confined to the eastern mainland, with no records of vagrants outside . Historically, the species' range was broader, reaching northward to the Suttor River in , but it contracted significantly during the late 19th and early 20th centuries primarily due to widespread clearance for . The current distribution remains patchy, consisting of isolated populations in coastal valleys and inland plains across its core range in , , and . As assessed by in 2024, the extent of occurrence for the turquoise parrot is approximately 771,000 km², reflecting its overall spread across southeastern , while the area of occupancy is unknown. As of 2024, the area of occupancy is estimated at around 20,000 km² (low reliability), with indications of increase in .

Habitat preferences

The turquoise parrot prefers open eucalypt woodlands dominated by species, such as box-ironbark associations, and callitris pine forests (Callitris spp.), particularly those with grassy understories. It shows a marked affinity for ecotones between these woodlands and native grasslands, as well as areas adjacent to farmland or heath. Key habitat features include native grass-dominated ground cover, which supports foraging, and the presence of tree hollows in live or dead trees for nesting, often in species like river red gums () along riparian zones near creeks. These riparian areas provide essential shelter and breeding sites, with hollows typically located in dead branches or trunks. The species occupies elevations between 0 and 1,130 m, primarily on inland slopes and tablelands of southeastern . It avoids dense forests, which lack suitable open understories, and arid desert regions beyond its moist temperate range. During the non-breeding season, turquoise parrots shift toward more open grassy areas to access abundant seeds, while maintaining use of treed corridors for dispersal. This local movement, often less than 10 km, reflects adaptations to seasonal resource availability within their preferred landscapes.

Behavior and ecology

Social behavior and movements

The turquoise parrot (Neophema pulchella) typically occurs in pairs or small family groups consisting of parents and their offspring, with group sizes ranging from 3 to 10 individuals during much of the year. Larger flocks of up to 30 birds may form post-breeding in autumn and winter, particularly when resources are abundant. These facilitate social interactions and resource sharing while minimizing predation risk in open habitats. The species is predominantly sedentary across its range in southeastern , exhibiting no long-distance . Instead, it undertakes local nomadic movements, often along treed corridors in response to fluctuations in food availability and rainfall patterns. These short dispersals allow populations to exploit seasonal resources without extensive relocation. Vocalizations play a key role in social cohesion, with soft twittering contact calls emitted during flight or on the ground to maintain group proximity and pair bonds. Sharper, high-pitched alarm notes, described as "zit-zit" or zitting calls, are used to signal threats and defend territories against potential intruders. These calls are generally subdued compared to larger parrots, reflecting the species' preference for inconspicuous behavior. Turquoise parrots form monogamous pairs that defend small nesting territories around cavity sites, with occasional displays of aggression toward conspecific intruders to protect breeding areas. Such interactions are brief and focused, helping to secure resources for the pair and their young without extensive territorial disputes.

Foraging and diet

The turquoise parrot (Neophema pulchella) is primarily granivorous, with the bulk of its diet comprising seeds from native and introduced grasses and herbs, such as Austrodanthonia spp., Poa annua, Anthoxanthum odoratum, and Briza spp.. It also consumes seeds from shrubs like common fringe-myrtle (Calytrix tetragona) and erect guinea-flower (Hibbertia riparia), as well as nectar from plants such as Grevillea alpina. Foraging occurs predominantly on or near the ground, often in pairs or small groups of 5–30 individuals, typically in open clearings, margins, pastures, and disturbed sites like verges and lawns where seeding are abundant. These actively feed from early morning through late afternoon, with a midday rest period, and show a for shaded areas that provide while searching for food. Brief references to social highlight coordinated movements in these groups to exploit patchy resources. Supplementary components of the diet include green plant material, flowers, fruits, and occasional insects such as scale insects, which provide protein, particularly during periods of higher nutritional demand. The turquoise parrot drinks water daily, typically twice per day at dawn and dusk, from sources like puddles, streams, or dams, a that influences its selection of habitats near reliable .

Reproduction and breeding

The turquoise parrot exhibits a monogamous , with pairs forming from communal flocks as the breeding season approaches. The breeding season typically spans primarily from August to December in eastern , peaking between October and November in many regions, with occasional breeding in April–May for second broods. Nesting occurs in tree hollows, often in living or dead or Callitris trees, at heights of 1 to 3 meters above the ground; pairs may also use stumps, logs, or artificial nest boxes. The female prepares the nest by lining the hollow with decayed wood dust, fine wood chips, leaves, or grass. Clutch sizes range from 2 to 6 glossy white eggs, with an average of 4 to 5; eggs are laid at intervals of 2 to 3 days. lasts approximately 18 to 22 days and is performed solely by the female, who leaves the nest briefly to feed or drink while the male remains nearby or provides food. Both parents share chick-rearing duties, with the female brooding the hatchlings for the first few days before the male assists in feeding them regurgitated seeds and soft foods. Chicks remain in the nest for about 4 weeks, fledging at 25 to 32 days of age, after which they depend on the parents for 1 to 4 additional weeks while learning to . In favorable conditions, pairs may raise a second brood in the same season. Breeding success yields an average of 2.3 to 2.8 fledglings per nesting attempt or successful nest.

Health and diseases

Known pathogens

The turquoise parrot (Neophema pulchella) is susceptible to a range of bacterial, viral, fungal, and parasitic pathogens, with infections more frequently documented in captive populations than in the wild, where direct evidence remains limited. Most data are extrapolated from congeneric Neophema species or general psittacines.

Bacterial Pathogens

, the causative agent of , induces respiratory distress, lethargy, and systemic infections in psittacine birds, including those in the Neophema genus; transmission occurs via inhalation of contaminated dust or droppings from infected birds. spp., acquired through contaminated food or water, lead to , , and septicemia in parrots, posing risks in captive settings where hygiene may be compromised.

Viral Pathogens

Psittacine beak and feather disease (PBFD), caused by the circovirus beak and feather disease virus (BFDV), results in progressive feather loss, beak and nail deformities, and immune suppression, often proving fatal in young or stressed individuals; while not confirmed in wild turquoise parrots, susceptibility is likely given its prevalence across Australian psittacines. Avian paramyxovirus serotype 3 (APMV-3) frequently affects Neophema spp., manifesting as mild respiratory symptoms, pancreatitis, and neurological signs such as ataxia, with higher mortality in dense aviary conditions.

Fungal Pathogens

, primarily due to *, targets the in immunocompromised or stressed psittacine birds, including those in the Neophema genus, causing granulomatous lesions, dyspnea, and ; spores are inhaled from environmental sources like moldy or feed.

Parasitic Pathogens

Internal parasites such as (e.g., spp.) infect the intestinal tract, leading to mucoid and , particularly in crowded captive flocks where oocysts spread via feces. External parasites including mites (Knemidokoptes spp.) can infest skin and follicles in psittacine birds, resulting in poor condition, itching, and secondary bacterial infections. The haemosporidian blood parasite Haemoproteus minutus has caused lethal outbreaks in captive turquoise parrots, with megalomeronts forming in tissues and inducing severe and organ damage.

Disease susceptibility and impacts

The turquoise parrot (Neophema pulchella) is likely susceptible to (PBFD), a circoviral that induces abnormalities, including , loss, and abnormal regrowth, which impair flight efficiency and diminish mate attraction by altering plumage vibrancy essential for displays. In juveniles, PBFD often manifests acutely, leading to high mortality rates that can reach up to 50% in infected nestlings of susceptible psittacine species, including those in the Neophema genus, due to and secondary s. Psittacosis, caused by , affects adult turquoise parrots with acute respiratory symptoms such as , lethargy, and weight loss, which reduce overall vitality and lower breeding success by impairing and egg viability. Outbreaks in wild psittacine populations, including natives, are frequently associated with environmental stressors like habitat degradation, which compromise immune function and facilitate bacterial transmission through aerosols from droppings or secretions. Due to its fragmented and small population sizes, the turquoise parrot demonstrates heightened vulnerability to introduced pathogens like PBFD and compared to more robust parrot species with larger, interconnected groups that buffer disease spread. This susceptibility is exacerbated by lower in isolated subpopulations, potentially reducing adaptive resistance to novel infections. Serological monitoring in has revealed PBFD exposure in wild psittacine birds, with historical surveys indicating prevalence rates of 41-94% across flocks. Ongoing emphasizes the need for vigilant screening to mitigate impacts on survival and reproduction in both wild and recovering populations.

Conservation status

Global and national assessments

The Turquoise Parrot (Neophema pulchella) is classified as Least Concern on the , with the assessment conducted in 2024. This status is attributed to its very large extent of occurrence exceeding 20,000 km²—specifically estimated at 771,000 km²—and a stable global population that does not approach vulnerable thresholds under population size criteria (over 10,000 mature individuals). At the national level in , the species was reassessed as Least Concern in the Action Plan for Birds 2020, despite ongoing regional declines in parts of its range. The global population is estimated at approximately 20,000 mature individuals (2009, poor), with low indicating a stable trend overall, though localized variations persist. efforts by authorities estimate that around 18,000 individuals—comprising about 90% of the total population—occur in (2009 estimate, low). Historically, the Turquoise Parrot experienced a severe decline to near- between 1880 and 1920, primarily due to habitat clearance and modification by introduced herbivores. However, populations have since recovered in regions such as , with sightings increasing from the 1930s onward following the species' presumed there by the early .

Regional variations and threats

In , the Turquoise Parrot (Neophema pulchella) is listed as Vulnerable under the Biodiversity Conservation Act 2016. Primary threats include the degradation of grasslands through livestock grazing, which reduces the availability of grass and forb seeds essential for foraging, and predation by introduced feral cats (Felis catus) and European red foxes (Vulpes vulpes), which target nests and adult females. These factors contribute to habitat stress across key bioregions such as the and tablelands, where over 50% of native forests and woodlands have been cleared historically. In , the species holds Vulnerable status under the Flora and Fauna Guarantee Act 1988, following a 2023 assessment. Major threats stem from inappropriate fire regimes that eliminate grasses used for feeding and nesting, as well as the loss of hollow-bearing trees due to and silvicultural practices, which limit suitable sites near the ground. These impacts are particularly acute in north-eastern regions like the Warby Ranges, where exacerbates vulnerability. Queensland lists the Turquoise Parrot as least concern under the Nature Conservation Act 1992. Threats are relatively minor but include urban expansion in southern areas such as near , which encroaches on open woodlands and grassy clearings vital for the . Across its range, poses a common threat through induced droughts that diminish seed availability in pastures and grasslands, potentially affecting foraging success and overall population stability. This aligns with broader national assessments indicating ongoing pressures from environmental variability.

Recovery and management efforts

Conservation efforts for the Turquoise Parrot focus on habitat protection, threat mitigation, and population monitoring to support its recovery from historical declines. A significant portion of the species' range in is encompassed by parks, such as Weddin Mountains National Park, and traveling stock routes that serve as vital connectivity corridors for movement and foraging. In , grassland reserves in the north-east and east regions provide key protected habitats, particularly for ground-foraging populations. In 2024, BirdLife Australia installed 120 custom-made nest boxes in north-eastern to support breeding. Management actions emphasize maintaining suitable nesting and foraging conditions. Retention of hollow-bearing trees in state forests is prioritized to ensure availability of nesting sites, as the species relies on tree hollows for breeding. Fox baiting programs target the European red fox, a major predator, with efforts aimed at reducing nest predation rates through coordinated control measures. Additionally, initiatives restore native grass understories degraded by and , enhancing food resources like seeds. Research and monitoring are led by organizations such as BirdLife Australia, which has conducted annual surveys since to assess distribution and abundance trends across key sites. Community-driven nest box programs supplement natural hollows, with installations on private lands and reserves increasing available breeding sites and supporting local population growth. As of 2025, no major new initiatives have been announced, but ongoing stable or increasing trends observed in monitoring data indicate potential for future downlisting from vulnerable status.

Aviculture

History and popularity

The turquoise parrot (Neophema pulchella) entered in the , shortly after its scientific description by George Shaw in 1792, becoming one of the earliest parrots kept as cage birds by European colonists and enthusiasts for its striking turquoise and yellow plumage and relatively quiet demeanor. Early imports to occurred during this period, contributing to its initial appeal among bird keepers who valued its small size and vibrant colors. In , the species gained traction in aviculture from the 1920s onward, coinciding with the recovery of wild populations after heavy trapping for the pet trade in the late 1800s had nearly extirpated it from some areas. Popularity surged globally after the 1980s, driven by advancements in techniques that improved survival rates and reduced reliance on wild-caught specimens, making the turquoise parrot a staple in aviaries worldwide. Its docile nature and ease of maintenance further endeared it to breeders, with the now commonly housed in collections across , , and . The discovery and propagation of color mutations, such as the blue variant first bred in Europe in 2010, added to its allure among aviculturists seeking genetic variety. In Australia, the turquoise parrot is fully protected under state wildlife laws, classified as vulnerable or near threatened in several regions, necessitating licenses or permits for keeping, breeding, and interstate trade to prevent overexploitation. Internationally, it has been listed under CITES Appendix II since 1981, regulating commercial trade to ensure sustainability. Culturally, the turquoise parrot holds significance in as a local in regions like the Glenrowan , often highlighted in avicultural events and as an emblem of native ecosystems amid conservation awareness efforts.

Captive breeding and care

In captivity, turquoise parrots (Neophema pulchella) require spacious aviaries to thrive, with a minimum size of 2 m in length by 1 m in width by 2 m in height for a breeding pair to allow for flight and . These enclosures should include natural perches such as branches of varying diameters, nesting boxes that mimic tree hollows (approximately 15 cm x 15 cm base and 25-30 cm deep with a 4.5-5 cm entrance hole), and enrichment items like swings and shallow bathing dishes. Temperature should be maintained between 15-25°C to prevent stress, with protection from drafts and extreme cold, while high levels (around 50-60%) support their natural bathing behaviors, facilitated by misters or pans of water. Breeding pairs typically reach between 12 and 24 months of age, with the season aligning to late winter through summer (August to January in the ). Females lay clutches of 3-6 eggs, which are incubated solely by the for 18-20 days, with fledging occurring after 4-5 weeks and juveniles remaining dependent for an additional 2-3 weeks. Successful breeding, achieving 70-80% hatch and fledging rates, depends on a nutrient-enriched diet during this period, including increased protein and calcium sources; pairs should be isolated to avoid or hybridization with other Neophema . The captive diet consists primarily of a small seed mix featuring canary seed, white millet, panicum, and limited oats, supplemented daily with fresh greens (such as spinach, kale, and lettuce), vegetables (carrots and broccoli), and small amounts of fruits (apples, pears, and berries) to replicate their natural foraging. Calcium supplementation via cuttlebone or powder is essential, particularly for breeding females, while oily seeds like sunflower should be minimized to prevent obesity; sprouted seeds and occasional insect-based foods (e.g., mealworms) enhance breeding outcomes. Health management in emphasizes protocols for new birds to screen for (PBFD) and , both prevalent in psittacines and transmissible via feathers, feces, or aerosols, with regular veterinary testing recommended. Aviaries must be kept clean and dry to mitigate risks of mites, respiratory infections, and internal parasites, with performed biannually. has produced color mutations such as opaline, which reduces for paler, yellow-shifted , established since the late , alongside blue, lutino, and pied variants; as of 2025, rare red-opaline combinations have been reported in specialized aviaries, increasing but requiring careful monitoring to maintain viability.

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