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Colchicum

Colchicum is a of approximately 163 species of perennial, cormous flowering plants in the family , native to temperate and subtropical regions spanning , the Mediterranean, , the , , and as far east as the western Himalaya and . These geophytes are distinguished by their hysteranthous growth habit, where goblet-shaped, crocus-like flowers—typically lilac, pink, purple, or white—emerge in autumn or spring from leafless stems, followed by broad, lanceolate leaves in the subsequent season. The , first described by in 1753, belongs to the order within the monocotyledons and is characterized by its reduced or absent stems, androecial nectaries, and 2–4-porate grains. Taxonomically, Colchicum forms a monophyletic group within , a family of about 15 genera and 250–300 , though it has undergone revisions incorporating former segregate genera like Androcymbium and Merendera based on molecular and morphological evidence. The plants propagate via corms, which are large, irregular, and covered in a dark-brown , producing 1–10 flower stalks per corm; flowers feature six tepals, six stamens, and a superior , with capsules that dehisce to release winged . Ecologically, thrive in well-drained soils in grasslands, meadows, rocky slopes, and woodlands, with many exhibiting adaptations to seasonal and some , such as the 14 endemic taxa in alone. Notable for both ornamental and medicinal value, Colchicum species are cultivated in gardens for their fall-blooming displays, hardy in USDA zones 4–9, and preferring full sun to partial shade with moist, humus-rich conditions. The genus is the primary natural source of , an extracted mainly from the corms and seeds of (meadow saffron), which has been used medicinally since ancient times for treating , , and by inhibiting and migration. However, renders all parts of Colchicum plants highly toxic, with ingestion causing severe gastrointestinal symptoms, multi-organ failure, and potentially fatal outcomes at doses as low as 7 mg, necessitating professional handling for any therapeutic applications.

Description

Botanical features

Colchicum species are herbaceous that arise from underground, tunicated corms, which serve as the primary storage and propagation organs. These typically reach heights of 15-40 cm, with slender, erect flowering stems emerging directly from the soil in many species. The corms are solid and fleshy, often producing offsets that contribute to . The flowers are solitary or few per corm, goblet- or funnel-shaped, and feature six petaloid s that are fused at the base into a tube extending to the . Tepal colors range from lilac and purple to pink, white, or yellow across , with lengths of 3-7 cm. In many taxa, flowering is hysteranthous, meaning blooms appear before the leaves emerge. The is superior and subterranean, cylindrical with three deep locules containing numerous ovules; it gives rise to three elongate styles, often exceeding 10 cm in length, which terminate in three-lobed stigmas. The androecium consists of six stamens arranged in two whorls, with filaments adnate to the tube and versatile anthers. All plant parts contain the colchicine, which is concentrated in the corms. Vegetative growth produces 4-8 basal leaves per , which are linear to lanceolate, dark green, and up to 30 cm long, with parallel venation and entire margins. These leaves lack the prominent white midrib characteristic of related genera. Colchicum belongs to the family in the order , a group of monocotyledonous plants distinguished by their and lilial affinities. The genus typically exhibits a diploid number of 2n=18, though occurs in some . Morphologically, Colchicum differs from similar genera like (Iridaceae) by its six stamens and three distinct styles versus three stamens and a single trifid style, broader leaves without a central white stripe, and longer styles emerging from a superior .

Life cycle and phenology

Colchicum are perennial geophytes characterized by a hysteranthous , in which flowering and leaf growth occur in distinct seasons. Flowers typically emerge in autumn, from late summer to early winter, often without accompanying leaves, relying on stored reserves from the for development. After and fertilization, the develops underground through winter. In spring, leaves emerge to photosynthesize and support fruit maturation, with the plant entering a summer period when foliage senesces and the above-ground parts die back, conserving energy in the until the next cycle. This temporal separation enhances survival in seasonal environments by avoiding overlap between reproductive and vegetative phases. Reproduction in Colchicum occurs both vegetatively and sexually. Vegetative propagation is primary, with the mother annually producing one or more daughter corms through division at its base, allowing clonal spread and colony formation over time. Sexually, is mainly entomophilous, facilitated by such as bees and flies attracted to the and . However, in some tropical southern , such as Colchicum burchellii and related taxa including C. melanthioides, rodent pollination predominates, with small mammals like Aethomys namaquensis transferring pollen on their fur and in feces while foraging on floral rewards. Following , capsules develop and dehisce in spring, coinciding with leaf emergence, to release seeds. Seeds often bear elaiosomes, lipid-rich appendages that attract ants for dispersal via in certain . In other , such as C. autumnale, dispersal is primarily barochorous, with seeds falling near the parent plant upon capsule dehiscence. As perennials, Colchicum exhibit , with individual corms capable of persisting for 5–15 years or more in suitable conditions, gradually deepening in soil through contractile roots and annual offsets.

Nomenclature

Etymology

The genus name Colchicum originates from the term kolchikón (κολχικόν), signifying "of " or "from ," an ancient kingdom located in the region of modern-day western near the , where plants of this were historically abundant. This linguistic root reflects the plant's geographical association with , a land renowned in antiquity for its botanical diversity and medicinal resources. The name's mythological ties trace to legends, particularly the story of , the Colchian princess and sorceress who, according to tradition, employed Colchicum species in her concoctions as both potent poisons and antidotes, earning the plant an early association with her name in some ancient texts. The physician and pharmacologist referenced kolchikón in his 1st-century AD work when describing the autumn-blooming , highlighting its toxic properties alongside its potential therapeutic uses. Carl Linnaeus formally described and validated the genus Colchicum L. in the first edition of his Species Plantarum in 1753, adopting the longstanding Greek-derived name without alteration. Post-Linnaean botanical nomenclature has preserved this etymology unchanged, maintaining its direct connection to the plant's ancient origins in Colchis mythology and geography.

Common names

Colchicum species are known by various vernacular names that often reflect their autumnal blooming habit, leafless flowering stems, or superficial resemblance to crocuses. The most widely used English common names include autumn crocus, meadow saffron, naked ladies, naked boys, wild saffron, fall crocus, wonder bulb, and mysteria. Other descriptive names allude to the phenomenon of flowers appearing before leaves, such as son-before-the-father, sons-before-the-fathers, and daughters-before-mothers. In total, around a dozen English vernacular names exist for the genus, though "colchicum" itself persists in horticultural and scientific contexts for clarity. Regional variations highlight local perceptions of the plant's appearance and seasonality. In parts of , names like "wild saffron" emphasize its crocus-like flowers and historical associations with the spice plant, while speakers use "colchique d'automne" and Germans "Herbstzeitlose" to denote its fall blooming. In , "tidlös" and "myrkkyliljat" (meaning "poison lilies") underscore the plant's . These names aid non-scientific identification but can lead to errors, particularly the confusion of Colchicum with , the true saffron crocus; while stigmas yield the edible spice , Colchicum contains toxic alkaloids like throughout its parts, making misidentification dangerous. The leafless flowering, which inspires names like "," further distinguishes Colchicum from true crocuses that bloom with foliage.

Taxonomy

Classification

Colchicum belongs to the kingdom Plantae, phylum Tracheophyta, class , order , and family , placing it among the monocotyledonous flowering plants characterized by parallel-veined leaves and scattered vascular bundles. This taxonomic hierarchy reflects the APG IV system's recognition of Colchicaceae as a distinct family within Liliales, separated from based on molecular and morphological evidence such as the presence of phenethylisoquinoline alkaloids and tunicated corms. The genus Colchicum L. was formally described by in his in 1753, with L. designated as the , anchoring the genus's nomenclatural stability. Within the genus, no formal subgenera are universally accepted, though informal groupings have been proposed to organize the approximately 163 species based on cytological features like numbers—typically ranging from 2n=18 (diploid) to 2n=108 or higher in polyploid forms—and geographic distribution patterns across temperate and . These informal categories aid in understanding intraspecific variation but lack the consensus required for formal . Post-2000 molecular phylogenetic studies have prompted significant reclassifications within Colchicum, expanding its circumscription to ensure monophyly. For instance, the genus Androcymbium Willd. was merged into Colchicum following analyses of plastid DNA sequences that demonstrated Androcymbium's paraphyly relative to Colchicum. Similarly, species formerly in Bulbocodium L. and Merendera Ramond ex DC. were incorporated based on multi-locus plastid data confirming their nested position within a broadened Colchicum clade, resolving long-standing morphological ambiguities in corm structure and floral traits. These revisions, supported by Bayesian and maximum parsimony methods, have stabilized the genus's boundaries while highlighting its evolutionary cohesion, though some authors argue for maintaining Merendera and Bulbocodium as separate genera due to distinct morphological traits.

Phylogenetic relationships

Colchicum belongs to the core of , which is sister to the Uvularia-Disporum (Uvularioideae), with Disporum representing a key relative in the latter group. The family diverged within approximately 50 million years ago during the Eocene, marking an early phase of monocot diversification in the order. Molecular phylogenetic studies using nuclear ITS and chloroplast matK genes have elucidated relationships within Colchicum, revealing African species as basal to the genus, with Eurasian lineages derived from this ancestral stock. These analyses, conducted in the 2010s, demonstrate strong for Colchicum and highlight biogeographic patterns where early divergences occurred in before radiation into . Evidence from plastid sequence data indicates ancient hybridization events between Colchicum and Bulbocodium, contributing to the synonymization of the latter genus into Colchicum due to their close evolutionary ties and shared morphological traits. In tropical lineages, such as those represented by C. coloratum, evolutionary shifts in pollination syndromes have occurred from insect pollination to rodent pollination, driven by adaptations like geoflorous inflorescences and nocturnal nectar production that favor small mammals over insects. This transition exemplifies within geophytic in southern ecosystems.

Distribution and ecology

Geographic range

The genus Colchicum is native to a broad region spanning , the , extending to the western Himalaya and the , including , and southward through tropical to . This distribution reflects the family's adaptation to diverse temperate and subtropical environments across the , with the majority of the approximately 160 species concentrated in and . The highest diversity occurs in the , particularly in and the , where environmental heterogeneity has driven . Turkey hosts 52 , 25 of which are endemic, establishing it as a primary center of diversity and for the genus. Similarly, Greece supports 31 , including 14 endemics, underscoring the region's role as a with significant taxonomic uniqueness. Several Colchicum species have been introduced outside their native ranges for ornamental purposes, notably in and , where species like C. autumnale are cultivated in gardens and occasionally naturalize in temperate zones without forming major invasive populations. Distribution patterns within the genus show temperate species, such as those in and , achieving widespread occurrence across continental climates, while tropical disjuncts are largely confined to montane regions in East and , where elevated habitats mimic cooler native conditions.

Habitats

Colchicum species primarily inhabit grassy meadows, open woodlands, rocky slopes, and scrublands throughout their native range in , , western and , and parts of tropical . These environments are typically characterized by seasonal moisture availability, with many species favoring well-drained, neutral to alkaline soils that prevent waterlogging around their subterranean corms. For instance, thrives in periodically wet to moderately moist grasslands, where it can tolerate partial shade from trees or open sunny exposures. Ecologically, Colchicum exhibits adaptations suited to these habitats, including drought-tolerant corms that enable summer during dry periods, allowing the to persist in Mediterranean climates with pronounced seasonal . Underground ovaries protect developing fruits from and herbivores, while the hysteranthous growth pattern—where leaves emerge in after autumn flowering—aligns with periods of increased rainfall and cooler temperatures. In Mediterranean species, seeds are often ant-dispersed via , with elaiosomes attracting that carry them to nests, enhancing dispersal in fragmented grassy or scrubby landscapes. Colchicum plays varied roles in its ecosystems, serving as a late-season nectar source for insect pollinators such as bees and moths in temperate and Mediterranean regions, thereby supporting pollinator networks during autumn when floral resources dwindle. In some African species, like those in the Succulent Karoo, pollination shifts to rodents, which are attracted to nocturnal nectar rewards and floral scents. Although leaves and flowers provide potential forage for herbivores such as deer, the presence of toxic alkaloids like colchicine limits consumption, reducing herbivory pressure and allowing populations to maintain density in shared habitats. Habitat preferences vary across the : temperate such as occupy moist grasslands and edges, while Mediterranean and montane tropical taxa, including those in Uzbekistan's high-elevation zones or South Africa's rocky hillsides, adapt to drier, saline, or sandy substrates in scrublands and subalpine meadows up to 4000 m. These variations reflect the 's broad tolerance for elevation and types, from fine-earth mountain substrates to saline plains.

Conservation

Status

The genus Colchicum comprises approximately 163 , many of which face conservation challenges due to their limited distributions and , particularly in biodiversity hotspots like the . While only a subset of these —estimated at 20-30% based on available assessments—have been formally evaluated under criteria, the evaluated taxa reveal a spectrum of risk levels, from Least Concern for widespread to for narrowly endemic ones. For instance, , a common , is classified as Least Concern globally due to its broad distribution across temperate regions. Several Colchicum species are assessed as threatened on the , highlighting elevated extinction risks in specific regions. Regional assessments indicate vulnerability for Colchicum luteum, such as Endangered in the due to and in northwestern and , though its global IUCN status is not formally evaluated. Similarly, Colchicum leptanthum is assessed as globally, with heightened vulnerability in its restricted range in eastern Anatolian steppes, including regional status in , where environmental changes exacerbate risks. Other examples include Colchicum macedonicum, rated Vulnerable in the owing to ongoing declines in habitat quality. Regional assessments further underscore varying risks across the genus's range. In , one Colchicum species, such as C. trigynum, is categorized as Near Threatened nationally, reflecting localized pressures in the despite broader stability. High endemism amplifies these vulnerabilities; for example, approximately 50% of the 31 Colchicum species in are endemic, primarily to Mediterranean islands and mainland montane areas, rendering them susceptible to range-restricted threats. Overall, with around 160 species globally and over 40 potentially at risk from narrow distributions in centers like the Mediterranean and , comprehensive evaluations are needed to better inform conservation priorities.

Threats and protection

Colchicum species face significant threats from , primarily driven by agricultural expansion and in Mediterranean hotspots. For instance, conversion of natural habitats to and developments has severely impacted populations of several species, including those in and . Overcollection of corms, particularly for medicinal purposes, poses a major risk to high-value species like Colchicum luteum, where increased demand has contributed to its rarity in regions such as the Himalaya. In , species such as C. kesselringii, C. luteum, and C. robustum are threatened by flower collection, by , and land conversion for and development, though a 2024 study assessing them as Least Concern under IUCN criteria notes stable populations based on field surveys conducted in September–October 2024. further exacerbates these pressures by altering phenological timing, as observed in Colchicum bulbocodium, where weather parameters like temperature and precipitation influence and flowering synchrony. Conservation efforts for Colchicum emphasize both in situ protection and ex situ strategies to mitigate these threats. In Turkey, several species benefit from safeguards in national parks, such as Colchicum baytopiorum in Termessos National Park (Antalya) and C. burttii in the Gelibolu Peninsula, where protected areas help preserve remnant populations. Uzbekistan has designated key reserves for Colchicum, including the Surkhan State Reserve, Hisor State Reserve, Nurota State Reserve, and Ugam-Chatkal National Park, which support species like C. kesselringii and C. luteum. Ex situ conservation includes seed banking initiatives; for example, the Chicago Botanic Garden maintains collections of Colchicum species as part of its tallgrass prairie seed bank efforts. Recent field surveys in Uzbekistan, conducted in September-October 2024, have assessed population statuses and advocated for maintaining natural areas to ensure long-term viability, with all studied species currently rated as Least Concern under IUCN criteria.

Cultivation

Ornamental use

Colchicum species are widely appreciated in for their striking autumn blooms, which emerge from the soil on leafless stems, resembling crocuses and providing vibrant color in temperate gardens during the fall season. These bulbous perennials thrive in well-drained soils and full sun to partial shade, making them suitable for a variety of landscape settings. They are particularly valued for their ability to naturalize over time, forming colonies that enhance garden aesthetics without requiring extensive maintenance. Hardy in USDA zones 4 through 9, Colchicum tolerates cold winters and is resilient in diverse conditions, including clay soils and neglect, allowing it to persist for years in borders and edges. Notable cultivars include 'Waterlily', celebrated for its large, fully lilac-pink flowers that evoke the layered petals of a water lily, and 'Pink Goblet', a compact selection producing up to six scented, goblet-shaped violet-purple blooms per . Species such as Colchicum kesselringii add variety with their distinctive striped patterns and spring flowering with leaves present, appealing to collectors seeking unique ornamental forms. In garden design, Colchicum excels in rock gardens, where its low-growing habit integrates seamlessly among stones, and in lawn naturalizations, where it creates drifts of color in and without competing aggressively with turf. It is also effective in mixed borders alongside late perennials, bridging the gap between summer and winter displays. The National Collection at in the UK preserves over 50 taxa, serving as a key resource for enthusiasts and demonstrating the genus's extensive ornamental potential. Colchicum has been cultivated in European gardens for ornamental purposes since at least the , with early introductions enhancing formal parterres and botanical collections.

Propagation

Colchicum species are primarily propagated vegetatively through division of offsets, which occurs during their summer period after foliage has died back. This method involves carefully lifting the clumps, separating the small cormlets from the parent , and replanting them immediately at a depth of about 10-15 cm in well-drained . Vegetative propagation maintains the genetic identity of the parent plant and is the most reliable approach for cultivars, as many hybrids exhibit sterility and do not produce viable seeds. Seed propagation is possible but considerably slower, often taking 2-3 years for seedlings to reach flowering size. should be sown fresh in autumn in a well-drained, gritty potting mix and subjected to natural outdoor conditions, including a period of summer warmth (around 20°C for 8 weeks) followed by cooling to 10-15°C to break and induce , which typically occurs in the following autumn or . Success with seeds requires patience, as rates can be low and erratic, with some viable seeds sprouting only after two years. For both methods, Colchicum thrives in well-drained, humus-rich sandy with a range of 6.0-7.5 to prevent from waterlogging. Poor is a major challenge, leading to , while pests such as slugs and snails can damage emerging shoots during . In sterile hybrids like Colchicum × byzantinum, seed is ineffective, necessitating reliance on .

Uses and toxicity

Medicinal applications

The primary medicinal compound extracted from Colchicum species is , an concentrated in the corms of C. autumnale at levels ranging from 0.3% to 0.8% of dry weight. This compound serves as the basis for therapeutic applications, functioning as an agent by binding to and inhibiting assembly, which disrupts and activation in . 's chemical structure features a trimethoxybenzene connected to a seven-membered through an intermediate seven-membered , contributing to its . Historical records indicate colchicine's use dates back to ancient civilizations, with the from around 1500 BCE describing Colchicum extracts for treating and joint swelling. In , recommended it for around 400 BCE, distinguishing the condition as an affliction of affluent lifestyles. Traditional systems continue this legacy; in , extracts from Colchicum luteum (known as Suranjan) are employed in formulations for to alleviate pain and inflammation. Colchicine is primarily extracted from the corms of C. autumnale through processes like ultrasound-assisted extraction, yielding purified for pharmaceutical use. The first of was achieved in the late 1950s, enabling production of analogs with modified rings to enhance efficacy or reduce toxicity. The U.S. (FDA) has approved for treating acute flares, with a standard regimen of 1.2 mg orally at the onset followed by 0.6 mg one hour later, not exceeding 1.8 mg in the first hour. It is also approved for prophylaxis and treatment of (FMF), at doses of 1.2–2.4 mg daily for adults and adjusted lower for children based on age and renal function. In June 2023, the U.S. approved 0.5 mg once daily (brand name Lodoco) to reduce the risk of cardiovascular events in adults with established atherosclerotic . Beyond approved indications, colchicine shows promise in investigational settings, including 2010s clinical trials exploring its antimitotic effects for by targeting dynamics in tumor cells. For , randomized trials have demonstrated its efficacy in reducing recurrence when added to therapy, with typical dosing at 0.5–1 mg daily for three months. In , it is used off-label for managing in horses to mitigate , though evidence remains limited to case reports and requires careful dosing due to risks.

Poisonous properties

All parts of Colchicum species contain the toxic alkaloid , rendering the plants poisonous to humans and animals upon . The concentration varies by plant part and , with bulbs, seeds, and flowers being particularly hazardous; for instance, , the most toxic , contains 0.4–0.6% colchicine in fresh bulbs and up to 1.8% in dried flowers. Accidental consumption, often mistaken for edible or onions due to similar appearance, can lead to severe , with doses as low as 0.5 mg/kg able to cause severe systemic and be , and ingestions exceeding 0.8 mg/kg carrying nearly 100% mortality risk, though deaths have been reported at even lower doses (e.g., 0.18 mg/kg). The manifests in three phases: an initial gastrointestinal stage (0–24 hours) characterized by intense , , watery , and , leading to and ; a multi-organ dysfunction phase (24 hours–7 days) involving (), , acute renal failure, , and cardiovascular collapse; and a recovery phase (>7 days) with rebound and potential alopecia in survivors. exerts its effects by binding to β-tubulin subunits, inhibiting polymerization and arresting at , which disproportionately impacts rapidly proliferating cells in the gut mucosa, , and follicles. This mechanism underlies the narrow therapeutic window, where medicinal doses (typically 0.5–1.2 mg/day for ) must be precisely controlled to avoid , and accidental plant ingestions can mimic through similar gastrointestinal hemorrhage and systemic failure. There is no specific antidote for colchicine poisoning; management is entirely supportive, focusing on early decontamination with multiple-dose activated charcoal (50 g in adults, 1 g/kg in children) to interrupt enterohepatic recirculation, aggressive fluid resuscitation, vasopressor support for , and intensive care for organ failure. Poisonings are particularly common in , such as on pastures contaminated with C. autumnale, resulting in bloody , , and fatal multi-organ effects. is regulated as a in many countries, classified under hazardous materials protocols (e.g., UN Poison Group III by the CDC), with strict controls on its pharmaceutical forms to prevent overdose. The ASPCA identifies Colchicum as highly toxic to dogs and cats, warning of severe , bloody , , and potential from even small ingestions, urging immediate veterinary intervention.

Diversity

Species overview

The genus Colchicum encompasses approximately 163 accepted , reflecting ongoing taxonomic revisions driven by molecular and morphological analyses. Of these, around 100 occur in , spanning from to the western Himalaya. The majority of species diversity is concentrated in the and western , with key centers of in regions like , the , and Transcaucasia. Phylogenetic studies using DNA sequence data have significantly reshaped the genus boundaries, leading to the inclusion of species from former genera such as Androcymbium (approximately 50 species) and Bulbocodium (approximately 15 species). These mergers, based on evidence of in Androcymbium relative to Colchicum, emphasize shared traits like acaulescent habits and androecial nectaries. Within Colchicum, informal infrageneric groupings highlight variation, such as clusters of white-flowered taxa; is prevalent, with common chromosome numbers ranging from 2n=18 to 2n=54, supporting evolutionary diversification through duplication. Taxonomic stability has been achieved through resolving over 200 historical synonyms across the , many stemming from 19th- and early 20th-century descriptions. The is Colchicum autumnale L., selected for its representative and wide distribution in temperate .

Notable species

, commonly known as meadow or autumn , is widespread across , particularly in meadows and woodlands from the to the . It produces lilac-purple flowers in early autumn before its strap-shaped leaves emerge in spring, and its corms are the primary natural source of , a compound used in treating and other inflammatory conditions. However, all parts of the are highly toxic due to this , causing severe gastrointestinal distress if ingested. Colchicum luteum, the yellow colchicum, is endemic to the , ranging from eastern to northern , where it grows at high elevations near the snowline. This species features bright yellow flowers emerging in spring and is considered endangered due to overexploitation for medicinal purposes and habitat loss from grazing and tourism. In Ayurvedic medicine, its corms are used to alleviate joint pain and , containing significant levels of . Colchicum melanthioides occurs in tropical and , from to , inhabiting subtropical grasslands and rocky slopes. It exhibits , a where small mammals like transfer via and , supported by rewards in its flowers. Colchicum speciosum, known as the showy meadow , is native to mountainous regions of northern , the , and northern , with five recognized subspecies varying in flower color from deep pink to lilac. It is prized ornamentally for its large, goblet-shaped flowers up to 8 cm long that bloom in autumn, often with a pale green tube and patterns on the petals. Colchicum troodii is an endemic species to , primarily in the , where it thrives in temperate shrublands and rocky areas from to 1,950 m elevation. Classified as Least Concern by conservation assessments, it produces lavender-pink flowers in autumn and is notable for its robust structure adapted to the island's . Among other notable species, Colchicum bulbocodium inhabits mountain meadows and blooms in with short-stemmed, funnel-shaped flowers in shades of lilac to purple, rendering it poisonous like many congeners. Colchicum cilicicum, distributed in , , and , features tall stems up to 30 cm with pinkish-purple autumn flowers, making it a favored ornamental in gardens. Colchicum graecum from displays early-blooming rose-pink flowers with tessellated patterns, contributing to the genus's diversity in the Mediterranean. Colchicum kotschyi ranges from to western and northern , growing on hillsides and used traditionally for its content in treating and . Colchicum lusitanum, found in , , , and northwest , is distinguished by its checkered tepals and wide adaptability, blooming in autumn up to 35 cm tall. Colchicum montanum in and produces small, ground-hugging flowers in early fall, highlighting the genus's variation in bloom timing. Colchicum persicum spans to , with purple-pink to violet autumn flowers adapted to diverse elevations, underscoring its ecological versatility in the . Colchicum triphyllum, distributed from the Mediterranean to northwest , is a spring- and autumn-flowering species rich in alkaloids and polyphenols, valued for potential pharmaceutical applications. Colchicum variegatum, native to southeastern and southwestern , bears striking checkered flowers in autumn, enhancing its ornamental appeal in temperate gardens.