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Alstroemeria aurea
Alstroemeria aurea
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Alstroemeria aurea
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Monocots
Order: Liliales
Family: Alstroemeriaceae
Genus: Alstroemeria
Species:
A. aurea
Binomial name
Alstroemeria aurea
Alstroemeria aurea is native to Chile and Argentina[1]
Synonyms[1]
  • Alstroemeria araucana Phil.
  • Alstroemeria aurantiaca D.Don
  • Alstroemeria chiloensis Phil.
  • Alstroemeria concolor Steud.
  • Alstroemeria mutabilis Kunze ex Kunth
  • Alstroemeria nivali Meyen
  • Alstroemeria peruviana Van Houtte
  • Alstroemeria pulchella E.Vilm.
  • Alstroemeria xanthina Phil.

Alstroemeria aurea is a species of flowering plant in the family Alstroemeriaceae, native to Chile and Argentina, but naturalised in Australia, New Zealand and the United Kingdom.[2] It is also widely cultivated as an ornamental.

Common names

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Common names include yellow alstroemeria,[2] though cultivars have been selected in a range of colours. The name Peruvian lily is often applied to this and other species of Alstroemeria, despite the fact that most are not native to that country.[citation needed]

Description

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Growing to 1 m (3.3 ft) tall by 0.5 m (1.6 ft) broad, it is a herbaceous perennial with brittle, fleshy roots beneath erect stems with narrow leaves. Many orchid-like flowers[3] in brilliant shades of yellow and orange. appear in early to midsummer. The flowers may be heavily spotted or striped with red or brown. If undisturbed, plants will spread rapidly in benign conditions.[4]

Cultivation

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When cultivated it is one of the hardiest alstroemerias, surviving temperatures of −10 °C (14 °F). It requires a sheltered spot in sun or part shade.[4]

Etymology

[edit]

The Latin specific epithet aureum means "golden".[5]

References

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Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
Alstroemeria aurea is a tuberous geophyte species in the family Alstroemeriaceae, native to the temperate biomes of central and southern and southern . This robust herbaceous forms spreading clumps with upright, branching stems that reach heights of 0.6 to 1 meter (2 to 3 feet), bearing narrow, lance-shaped, twisted leaves up to 10 cm long. In early to mid-summer, it produces terminal clusters of small, orchid-like flowers in shades of brilliant orange or golden-yellow, typically featuring six petals with darker spotting and streaking on the upper ones. Despite its common names of Peruvian lily or Inca lily—derived from the genus's association with South American flora—A. aurea originates primarily from Chilean regions spanning latitudes 32° to 49°S, inhabiting humid valleys and coastal mountains at altitudes of 300 to 1250 meters. It has been introduced and naturalized in parts of Australia, New Zealand, and Europe, where it thrives in similar temperate conditions. Hardy to USDA zones 7–10, the plant tolerates frost down to -15°C and occasional snow, making it suitable for outdoor cultivation in mild climates. In , A. aurea is prized for its long-lasting , which remain vibrant in vases for over two weeks, and its ability to attract pollinators while resisting deer. It prefers full sun to partial shade and organically rich, moist but well-drained soils with neutral to slightly acidic , though it adapts to various soil types including and . Propagation occurs via division in spring or fall, and it serves both ornamental and minor edible uses in its native range. The species contributes to in its , supporting local ecosystems through its nectar-rich blooms.

Taxonomy

Classification

Alstroemeria aurea is classified in the kingdom Plantae, phylum Tracheophyta, class Liliopsida, order Liliales, family Alstroemeriaceae, genus Alstroemeria, and species A. aurea. The species was first described by Robert Graham in 1833 in the Edinburgh New Philosophical Journal. Historically, Alstroemeria aurea was placed within the family Liliaceae due to superficial similarities in floral structure, but molecular phylogenetic studies in the 1990s, including analyses of DNA sequences, demonstrated distinct evolutionary lineages, leading to its reclassification into the separate family Alstroemeriaceae by the Angiosperm Phylogeny Group in 1998. This separation was further supported by morphological traits such as rhizomatous growth and chromosome characteristics unique to Alstroemeriaceae. Several names have been synonymized with Alstroemeria aurea, including Alstroemeria aurantiaca D. Don (1833), Alstroemeria araucana Phil. (1873), Alstroemeria chiloensis Phil. (1858), and Alstroemeria mutabilis Kunze (1850), as subsequent taxonomic revisions determined these to represent the same taxon based on type specimens and overlapping distributions in southern . No formal are currently accepted for Alstroemeria aurea, though populations in central and southern exhibit morphological variation in flower color and leaf pubescence, suggesting potential for infraspecific taxa pending further integrative taxonomic studies.

Common names and etymology

The genus is named after the Swedish botanist and naturalist Clas Alströmer (1736–1794), a close friend and pupil of , who received bulb specimens of South American plants collected by Alströmer's associates during expeditions in the late . The specific epithet aurea derives from the Latin aureus, meaning "golden," in reference to the plant's characteristic yellow to orange flower coloration. Alstroemeria aurea is known by several common names reflecting its South American origins and appearance, including Peruvian lily—a term linked to its Andean habitat despite its native range in and adjacent —lily-of-the-Incas, and golden Peruvian lily. In , regional names include amancay and Chilean lily, highlighting its local cultural significance. The genus comprises approximately 128 in the Alstroemeriaceae, primarily from and western . Specimens of A. aurea were among the first Alstroemeria plants collected in the 18th century by Alströmer's associates during botanical explorations in , contributing to early European introductions of the genus.

Description

Morphology

Alstroemeria aurea is a tuberous that forms spreading clumps from fleshy, horizontal rhizomes, which can reach up to 30 cm in length and produce offsets for clonal . The plant exhibits an upright growth habit, with simple to branched stems arising from the rhizomes and attaining heights of 60-120 cm. These stems are typically glabrous and support spirally arranged leaves along their length. In mild climates, the foliage remains semi-evergreen, persisting through winter. The leaves are grass-like, linear to lanceolate or oblanceolate in shape, measuring 5-10 cm long and 5-15 mm wide, with a green coloration that may include reddish markings toward the base. A is their resupination, where the leaves twist 180 degrees at the base, orienting the upper surface outward. The leaves are glabrous or sparsely hairy, bluntly acute to obtuse at the apex. Flowers are arranged in terminal umbels containing 5-20 lily-like blooms, each with six tepals that lack differentiation into sepals and petals. The tepals measure 2-3 cm long, with the outer three shorter (15-20 mm), acute, and slightly spreading or reflexed, while the inner three are longer (20-25 mm), obtuse, and saccate at the base. Flower color varies from to deep orange, often featuring prominent or dark spots and streaks, particularly on the inner tepals. In its native range, blooming occurs from June to July. Some populations exhibit variations in stem pubescence, with glabrous forms predominant, while flower coloration ranges continuously from pale yellow to intense orange-red. The rhizomes bear thin, tuberous that contribute to the plant's clump-forming nature.

Reproduction

Alstroemeria aurea exhibits hermaphroditic flowers that are self-compatible, yet strong during seed development promotes primarily pollination, with a selfing rate of approximately 0.3. The flowers display protandry, featuring a male phase lasting about 4 days, followed by a 1-day neuter phase and a 3-day female phase, which synchronizes across ramets to facilitate transfer between clones while minimizing . occurs from June to August in the native winter or during summer in cultivation. Pollination in A. aurea is entomophilous, relying on insects for pollen transfer, as the species is entirely dependent on biotic agents and lacks autonomous self-pollination capabilities. Nectar guides, consisting of contrasting spots on the tepals, direct pollinators toward the nectar and reproductive organs, enhancing visitation efficiency. In its native range, primary pollinators include bumblebees, which are attracted to the nectar secreted differentially across sexual phases, with higher production during the male phase. The tepal arrangement, with outer and inner whorls forming an orchid-like bloom, supports effective pollinator contact during visits. Successful leads to production within dehiscent capsules that contain multiple , though results in significantly lower set and size compared to or open-pollination due to effects. lack specialized long-distance dispersal structures and are primarily scattered locally from the ripening capsules through and ballistic dehiscence, remaining in close proximity to the parent plant. of these requires cold stratification, typically a period of 4–6 weeks at around 5°C (41°F), to overcome and initiate growth. In addition to sexual reproduction, A. aurea propagates vegetatively via rhizomes, which produce offsets annually and enable clonal expansion across suitable habitats. These store nutrients and facilitate division, allowing the to form dense stands over time. As a herbaceous , A. aurea completes a multi-year life cycle, persisting through seasonal and regrowth, with individual plants capable of surviving several years in natural populations. Seed viability is maintained for several months under cool, dry storage conditions, though fresh sowing is recommended for optimal germination rates.

Distribution and habitat

Native range

Alstroemeria aurea is native to central and southern , spanning from the in the north to the Aisén Region in the south, and extends into adjacent western , particularly the provinces of , Río Negro, and Chubut. This distribution corresponds to latitudes approximately 30°S to 46°S, primarily along the Andean foothills and coastal ranges. The species thrives at elevations ranging from 0 to 2000 meters, where it occupies diverse topographic positions including slopes and valleys. Within its native range, A. aurea prefers habitats such as moist meadows, stream banks, and edges of forests, transitioning between Mediterranean climates in the north and temperate conditions in the south. It grows in well-drained sandy-loam soils that support its rhizomatous growth, with annual rainfall typically between 500 and 1000 mm, including areas influenced by coastal fog and short dry seasons. Associated vegetation includes native grasses, sclerophyllous shrubs, and co-occurring species, forming part of the in open woodlands and grasslands. The plant exhibits adaptations suited to its variable environment, including once established through efficient in rhizomes, frost hardiness down to -15°C, and seasonal during prolonged dry periods. Populations typically form dense clumps in undisturbed open areas, contributing to local , but become rare in overgrazed zones where herbivory disrupts . These rhizomatous structures also enhance stability on slopes and margins.

Introduced ranges and invasiveness

Alstroemeria aurea has been introduced and naturalized outside its native range primarily through the trade, escaping from gardens as early as the . In , it is established in southeastern states including Victoria, , and , where it has become an environmental weed in regions such as the , , and near Falls Creek. In , the species naturalized around 1945 and is now widespread on both the North and Islands, often regarded as a pest plant due to its rapid spread. In , it is introduced and recorded as an alien species in the and listed in inventories such as DAISIE, with cultivation noted in , though less extensively naturalized compared to the . The plant's invasiveness stems from its ability to form dense stands via spreading rhizomes and thin fleshy roots, particularly in grasslands, riparian zones, and upland habitats with moderate shade. In , it competes with native vegetation and is considered a rampant spreader, prompting recognition as an in many areas. In , it displaces local in cooler temperate and sub-alpine environments, leading to its inclusion on regional weed lists in places like Sherbrooke Forest and the Blue Mountains. While not globally invasive, its establishment is facilitated by climatic similarities to its native Chilean and Argentinean habitats, and it poses medium ecological risk in affected regions. Management efforts focus on prevention and eradication in sensitive ecosystems, including manual removal by digging out tubers and rhizomes, especially for small infestations. Herbicide applications, such as glyphosate applied via cut-stump or foliar spray methods, are commonly used for larger populations, with follow-up monitoring required due to the plant's regenerative capacity. In Victoria, Australia, early invader protocols emphasize integrated control to limit further spread in conservation areas. Overall, A. aurea is monitored in introduced ranges, with ongoing vigilance in the ornamental trade to curb new introductions.

Ecology

Pollination and interactions

Alstroemeria aurea is primarily pollinated by native bumblebees in its Chilean range, with workers of Bombus dahlbomii accounting for over 90% of floral visits and serving as the most efficient pollinators on a per-visit basis. The protandrous nature of its flowers, characterized by temporal separation of male and female phases, promotes outcrossing, while differential nectar secretion—higher during the female phase—further encourages pollen transfer by these visitors. Pollen is collected efficiently by bumblebees through vibration, and the flowers' nectar guides, including ultraviolet-absorbing spots visible to pollinators, direct insects to nectaries and enhance deposition on stigmas, improving overall pollination success. Herbivory significantly influences A. aurea's interactions; introduced ungulates such as deer and reduce plant density via and in native forests, indirectly lowering visitation rates and reproductive output by altering floral neighborhood density. herbivores directly damage flowers, affecting both male ( export) and female (seed set) fitness components. Defoliation from such herbivory also reduces production and attraction, compounding these effects. In introduced regions like and , where A. aurea has naturalized as an environmental weed, pollination shifts to non-native and other , including honeybees, which visit flowers for and . This species supports trophic interactions by providing resources to these pollinators. As of April 2025, it has been highlighted as a potential invasive weed in due to its availability in garden stores, raising concerns about further environmental spread.

Conservation status

Alstroemeria aurea has not been assessed by the due to its widespread occurrence in native habitats across central and southern and adjacent . Despite this, local populations face declines from habitat loss driven by agricultural expansion and associated land conversion, particularly in lowland areas where burning and cropping activities disrupt suitable moist forest and environments. by further exacerbates these pressures by damaging rhizomatous growth and reducing regeneration in open sites. In non-native regions, A. aurea has naturalized and exhibits invasive tendencies in places like and , forming dense stands in grasslands and forests, though this does not directly impact native conspecific populations. The species benefits from protections within Chilean national parks, including Conguillío, where it occurs in undisturbed volcanic soils and forests, safeguarding key populations from direct human impacts. It is not included in the appendices of the Convention on International Trade in Endangered Species (), reflecting low trade-related risks. Overall population trends remain stable, supported by the species' adaptability and efforts in botanic gardens that maintain living collections for and reintroduction potential. Ongoing monitoring is recommended, particularly for across populations, to enhance resilience against climate-induced changes.

Cultivation

History of use

Alstroemeria aurea was first collected in during expeditions in the 1760s sponsored by the Swedish naturalist Clas Alströmer, whose travels to from 1760 to 1764 yielded specimens that formed the basis for the . The species was formally described by Robert Graham in 1833, based on material from Chilean collections, marking its recognition as a distinct within the Alstroemeriaceae family. Indigenous communities in have historically utilized the tubers of Alstroemeria aurea for medicinal purposes, particularly for their and pain-relieving properties in traditional remedies, though pre-colonial records remain limited due to sparse documentation. The species was introduced to in the late 18th century through botanical exchanges facilitated by Alströmer's networks, with early cultivation occurring in prominent gardens such as those at , where it was propagated as an exotic ornamental. By the , A. aurea gained popularity in European greenhouses for its vibrant orange-yellow blooms, serving as a foundational parent for hybrid development in temperate climates. In the , Alstroemeria aurea emerged as a key contributor to the global cut-flower industry, valued for its long vase life and adaptability to commercial production, with intensive breeding programs producing hybrids like the 'Friendship' series for enhanced color variety and stem strength. These developments, accelerating since the , have positioned alstroemerias, including those derived from A. aurea, as a major export crop from regions like the and . Culturally, Alstroemeria aurea symbolizes friendship and mutual support in modern , reflecting its twisted leaves as emblems of life's challenges overcome together. In Andean folklore, it holds minor significance tied to themes of , , and , with indigenous legends associating its blooms with gestures of deep and divine favor in pre-Columbian traditions.

Growing requirements

Alstroemeria aurea thrives in USDA hardiness zones 7 to 10, where it can tolerate light frost but benefits from mulching in colder areas to protect the roots during winter. It performs best in full sun to partial shade, appreciating afternoon shade in hot summer climates to prevent scorching. These preferences parallel its native habitat in the cool, moist , where it grows in well-drained mountain soils. For optimal growth, plant in well-drained, fertile that is organically rich and slightly acidic with a of 6 to 7; amend heavy soils with to improve drainage and . Waterlogging must be avoided, as it leads to , so ensure the site has good drainage to mimic its natural conditions. Watering should be moderate, providing about 25 mm (1 inch) per week during the active growth period in spring and summer to maintain even without saturation. Once established, the plant becomes somewhat drought-tolerant, requiring less frequent except during prolonged dry spells. Apply a balanced NPK , such as 6-6-6, in early spring to support blooming, but avoid excess , which can promote weak stems and excessive foliage at the expense of flowers. Common pests include slugs, aphids, spider mites, and thrips, which can be managed with appropriate insecticides or barriers; diseases such as occur in overly wet soils. The plant is deer-resistant due to its bitter taste from the toxin tulipalin A. As one of the hardier species in its , Alstroemeria aurea typically flowers 8 to 12 weeks after planting rhizomes in spring, producing blooms from early to mid-summer.

Propagation methods

Alstroemeria aurea is commonly propagated vegetatively through division of its rhizomes, a method that preserves the clonal nature of the and ensures uniformity in horticultural production. This process is ideally carried out in late winter or early spring during , when the clumps are lifted carefully to avoid damaging the brittle roots. Each divided section should include at least one growth bud or offset, which is then replanted 15 cm deep and spaced 30-45 cm apart in well-drained, organically rich soil to promote establishment. Vegetative typically achieves high success rates and allows to reach flowering maturity within one year. Seed propagation offers an alternative for introducing but is less favored due to inconsistent results and extended timelines. Fresh seeds collected in autumn should be scarified lightly to break , followed by cold stratification at 4-7°C for 4-6 weeks to mimic natural conditions and enhance viability. Sown in a sterile, well-draining medium, occurs over 20-60 days at 15-25°C, though rates remain low (often below 20% without treatment) without proper pretreatment. Seed-raised plants generally take 2-3 years to flower, making this method suitable for breeding rather than rapid commercial multiplication. In commercial settings, via is widely used to generate virus-free planting stock, addressing limitations of traditional methods like transmission in divisions. Explants from rhizomes, , or thin sections are cultured on Murashige-Skoog medium supplemented with cytokinins (e.g., benzyladenine) and auxins (e.g., naphthaleneacetic acid), yielding 4-11 shoots per explant depending on the protocol and . This technique facilitates high-volume production of healthy, uniform plants, often integrated with thermotherapy or meristem excision for elimination. Propagation efforts are most successful when initiated in spring under controlled conditions, with vegetative approaches outperforming in speed and reliability. Key challenges include slow rooting of offsets, which can take several weeks, and susceptibility to fungal pathogens like during stratification or early establishment, mitigated by ensuring excellent drainage, sterility, and avoiding overwatering.

References

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