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Hakea laurina
Hakea laurina
Hakea laurina
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Hakea laurina
Hakea laurina inflorescences at different stages of maturity
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Order: Proteales
Family: Proteaceae
Genus: Hakea
Species:
H. laurina
Binomial name
Hakea laurina
Occurrence data from AVH
Detail showing crimson flower head

Hakea laurina is a shrub or small tree commonly known as kodjet or pin-cushion hakea[3] and is endemic to Western Australia. The Noongar name for the plant is kodjet or kojet.[4] It has red and cream conspicuous globular flowers and lance shaped leaves.

Description

[edit]

Hakea laurina is an upright shrub or small tree with smooth grey bark, 2.5–6.0 m (8 ft 2 in – 19 ft 8 in) high, 3–5 m (9.8–16.4 ft) wide and does not form a lignotuber. The inflorescence consists of 120-190 conspicuous white, deep pink or red pin cushion shaped flowers in the leaf axils. The pedicels are 5.5–9.5 mm (0.22–0.37 in) long and smooth. The perianth is dark pink to red, the pistil 14–19.5 mm (0.55–0.77 in) long, cream-white or occasionally red or dark pink. The flower buds are enclosed in scale-like bracts. Flowering occurs from April to July. The leaves are simple, slightly blue green, flat, smooth, margins entire, lance or egg-shaped and taper to a blunt point at the tip. The leaves are arranged alternately along the branches, 7–21 cm (2.8–8.3 in) long, 6–29 mm (0.24–1.14 in) wide on a stem 1–2 cm (0.39–0.79 in) long and narrowing at the base. The fruit are in clusters of 1-10 per axil, 2.2–3.8 cm (0.87–1.50 in) long, 1.6–2.3 cm (0.63–0.91 in) wide, egg-shaped, smooth, occasionally with rough pitting and ending in a short beak.[3][5][6]

Taxonomy and naming

[edit]

Hakea laurina was first formally described in 1830 by Robert Brown and the description was published in Supplementum primum prodromi florae Novae Hollandiae.[7] The specific epithet is derived from the Latin laurus with reference to the resemblance of the leaves to laurel.[5]

Distribution

[edit]

Pincushion hakea is endemic to the coastal southwest of Western Australia, the northernmost range being Narrogin and extending east to Esperance.[8]

The habitat is often sandplains, sometimes occurring on sandy clay; most recorded specimens are in the southern districts of its botanical province. Introduced populations are known to exist on Kangaroo Island and in the Mount Lofty Ranges in South Australia.[1]

Cultivation

[edit]

The plant, which is propagated from seeds, is used in cultivation in the eastern states of Australia, and as a hedging or street plant in America and Italy.[5] Adaptable to a number of soil types, the plant is also tolerant of frost. The uses of this species include ornament and shading in public streets, wildlife habitat, windbreaks, and control of soil erosion.[9][10][11]

Conservation status

[edit]

Hakea laurina is listed as Vulnerable on the IUCN Red List of Threatened Species due to a suspected decline of at least 30% over the past three generations of the species, mainly due to land clearing for agriculture. The remnant subpopulations along road verges are threatened by further clearance for road maintenance, as well as weed invasion, pollution from phosphate fertilizers used in farming and altered fire regimes resulting in insufficient fire frequency.

The species is found within the protected areas of Cape Arid National Park, Fitzgerald River National Park, Stirling Range National Park and Lake Magenta Nature Reserve. Additional conservation actions required for the species include maintaining and managing threats of the populations along road verges, as well as regular monitoring of populations.[1][12]

References

[edit]
[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Hakea laurina

View on Grokipedia
from Grokipedia
Hakea laurina, commonly known as the pincushion hakea or sea urchin hakea, is a species of or small in the family , endemic to southwestern . It typically grows to a height of 3–6 meters with a rounded, spreading canopy up to 4 meters wide, featuring leathery, narrow-elliptical leaves that are 10–20 cm long and grey-green in color. The plant produces distinctive globular flower heads, up to 5 cm in diameter, with cream styles and red perianths that cluster on short stalks, blooming profusely from late autumn to early winter and attracting nectar-feeding birds and . Native to the region's mallee shrublands and heathlands, Hakea laurina thrives in well-drained sandy or loamy soils, often with clay undertones, and tolerates full sun, moderate frost, and drought once established. Its distribution spans from near Perth southward to Albany and eastward past Esperance to Cape Arid National Park, where it plays a role in local ecosystems by providing and food sources. The lacks a , making it reliant on seed regeneration after fire, and is classified as Vulnerable by the IUCN due to , though planting restrictions apply in some areas due to its potential invasiveness near sensitive bushland. Widely cultivated for its ornamental value, Hakea laurina is valued in gardens, parks, and as a or , particularly in mild climates like those of coastal , parts of , and the . It prefers acidic to neutral, phosphorus-poor soils and is propagated easily from seed or cuttings, though it can be susceptible to root-rot in heavy, wet conditions. The 's bold foliage and vibrant, pincushion-like blooms make it a standout feature in native , contributing to in revegetation projects while requiring careful site selection to prevent weed-like spread.

Description

Growth habit

_Hakea laurina is an upright or small that typically reaches a height of 2.5–6 m and a width of 3–5 m. It features a dense, rounded canopy formed by its branching pattern, which supports a compact structure particularly in full sun exposure. The plant exhibits smooth grey bark along its branches and trunk, contributing to its overall aesthetic and structural integrity. Unlike many co-occurring Proteaceae species, Hakea laurina lacks a , rendering adult plants highly susceptible to with near-complete mortality following intense burns. Regeneration occurs solely from serotinous seeds stored in canopy-held follicles, a strategy that underscores its to infrequent regimes in semi-arid environments. This non-sprouting habit can lead to population declines in areas with short intervals, as seedlings require over six years to mature and replenish seed banks. The species demonstrates a fast growth rate in well-drained, sandy soils typical of its native southwestern Australian , with branching that promotes dense foliage to optimize retention and shade in arid conditions. This architecture allows it to thrive in open, low-rainfall landscapes, forming key structural components in mallee-heath and communities.

Leaves

The leaves of Hakea laurina are simple, flat, and lanceolate to elliptical in shape, typically measuring 7–21 cm long and 6–29 mm wide, with entire, smooth margins that are clearly widest above the middle. They display a to grey-green coloration and are glabrous, with prominent venation that enhances their visual appeal. This foliage often waves or curls slightly, contributing to the plant's distinctive, laurel-like appearance. Arranged alternately along the branches, the leaves are widely spaced, creating a dense yet open canopy that allows light penetration. This patterning supports efficient exposure to while minimizing shading among individuals. The sclerophyllous texture of these leaves, marked by their thick, leathery consistency, enables effective water retention and sustained in arid, phosphorus-impoverished climates characteristic of southwestern . This is crucial for the species' survival in Mediterranean-type environments with seasonal , where the rigid structure reduces losses without compromising carbon fixation.

Flowers and inflorescence

The of Hakea laurina are dense, globular heads that measure up to 5 cm in diameter and consist of 120–190 small flowers clustered tightly together. These heads are positioned axillary on well-ripened wood, nestling among the leaves without being obscured. Each flower features a glabrous that is 4–6 mm long and deep pinkish-red in color, surrounding a prominent pistil with a cream-white style measuring 14–19.5 mm long that projects outward, creating the characteristic appearance. The styles may fade to pale pink as the flowers age. Flowering typically begins in late April, peaks in July during mild winters, and concludes by late August in . The flowers produce copious and emit a faint, pleasant fragrance, serving as key attractants for pollinators including birds.

Fruits and seeds

The fruits of Hakea laurina are woody follicles that measure 22–38 mm in length and 16–22 mm in width, typically presenting as grey, egg-shaped structures with a smooth surface and a short . These follicles often develop in clusters originating from a single and exhibit a serotinous nature, remaining tightly closed on the plant for extended periods to protect the enclosed from predation and environmental stress. This serotiny ensures that the follicles open only in response to intense from bushfires or upon the death of the parent , thereby synchronizing release with post-disturbance conditions favorable for regeneration. Each follicle splits along one suture to liberate two seeds, a trait common among serotinous adapted to fire-prone ecosystems. The seeds are ovate in shape, 15–24 mm long (including the ) and 10–15 mm wide, featuring a blackish-brown to black discontinuous marginal that extends broadly down both lateral sides and narrowly around the base, optimizing them for anemochory or wind dispersal over short distances. is triggered by cues such as shock or exposure to smoke-derived chemicals, which scarify the seed coat and stimulate enzymatic activity, leading to higher rates of in ash-enriched soils with reduced competition from established vegetation.

Taxonomy

Etymology and naming

Hakea laurina was first formally described by the English botanist Robert Brown in 1830, based on specimens he collected in in 1801 during his expedition with aboard HMS Investigator. The description appeared in Brown's Supplementum primum prodromi florae Novae Hollandiae, a key work in early Australian that expanded on his 1810 Prodromus florae Novae Hollandiae et Insulae Van Diemen, documenting the continent's diverse flora amid European exploration and colonial expansion. The specific epithet laurina derives from the Latin laurus, referring to the laurel tree (Laurus nobilis), with the suffix -ina indicating resemblance; this alludes to the plant's leaves, which Brown noted as similar to those of laurel in shape and arrangement. Common names for Hakea laurina include pincushion hakea and sea-urchin hakea, reflecting the spherical, pin-like clusters of its flowers. In the Noongar language of Indigenous peoples in southwestern , it is known as kodjet or koordjit, highlighting its cultural significance in traditional knowledge systems.

Classification and phylogeny

_Hakea laurina is a species within the family and the , which includes approximately 150 species of shrubs and small trees endemic to . The is characterized by its diversity in southwestern , where the majority of species, including H. laurina, are concentrated. In modern taxonomic treatments, lacks a formal infrageneric , with grouped informally based on morphology and phylogeny. H. laurina belongs to the Petiolaris Group, a small assemblage of three restricted to southern , and is closely related to H. petiolaris and H. obtusa, from which it differs in leaf width, fruit morphology, and positioning. It also shows affinities to in the Varia Group, such as H. varia, through shared traits like woody fruits. Phylogenetic analyses place H. laurina within of the genus , one of two major clades resulting from an early divergence around 10 million years ago. This encompasses about 96 with obscure leaf venation and discoid presenters. is ancestral in , including in the lineage leading to H. laurina, with subsequent divergences producing multiple bird-pollinated subgroups amid shifts to in other branches. No subspecies of H. laurina are recognized, and its taxonomy has remained stable since its description by Robert Brown in 1830, with no major revisions proposed in contemporary floras.

Distribution and habitat

Native range

Hakea laurina is endemic to southwestern Western Australia, where it occurs in coastal and near-coastal regions. Its native distribution spans approximately 400 km, extending from Narrogin in the north to Esperance in the east. More specifically, wild populations are documented from Wagin southward to Denmark and eastward to Israelite Bay along the south coast. The species is present across multiple Interim Biogeographic Regionalisation for Australia (IBRA) bioregions, including the Avon Wheatbelt, Esperance Plains, Jarrah Forest, Mallee, and Swan Coastal Plain, as well as subregions such as Eastern Mallee, Fitzgerald, Katanning, Northern Jarrah Forest, Perth, Recherche, Southern Jarrah Forest, and Western Mallee. Early botanical collections from the , shortly after European settlement began in the region, align closely with the current documented range, suggesting historical stability in its distribution prior to broader land-use changes. Beyond its native , Hakea laurina has established introduced populations on and in the of , where it has naturalised.

Environmental preferences

_Hakea laurina thrives in sandy, well-drained soils within heathlands and woodlands of southwestern Australia, where it occupies nutrient-deficient substrates often characterized by low availability. These environments include jarrah forests, mallee-heaths, and scrub-heaths on sands, gravels, or lateritic profiles, supporting its adaptation to oligotrophic conditions through specialized root structures like cluster roots that enhance uptake. The species favors a regime with dry summers and wet winters, receiving an annual rainfall of 400–600 mm, as exemplified by sites in the Fitzgerald River National Park where mean is approximately 452 mm. It tolerates periodic and is resilient to the seasonal temperature fluctuations of this region, with summer maxima around 28°C and winter minima near 16°C. Hakea laurina exhibits tolerance to coastal exposure and salt spray, enabling persistence in and near-shore habitats. It can endure occasional waterlogging in sandy flats or along creeks, though prolonged saturation is unfavorable. In its native range, it commonly associates with Eucalyptus-dominated woodlands and heath communities, contributing to sclerophyllous vegetation structures.

Ecology

Pollination

Hakea laurina exhibits , a primarily mediated by birds. The is classified as bird-pollinated based on floral traits such as a stigma–nectary distance exceeding 13 mm, which favors access by pollinators with longer bills. The principal pollinators are nectar-feeding honeyeaters (family Meliphagidae), including the (Phylidonyris novaehollandiae), which are attracted to the plant's large, conspicuous red inflorescences. These birds probe the flowers for the abundant , inadvertently transferring via their bills and heads. Floral adaptations, including protruding styles and high (accessibility index log₁₀ ≥ 5.00), enhance efficiency for avian visitors while limiting access for smaller pollinators. Flowering occurs from late autumn through winter, typically starting in April, peaking in July, and concluding by August in mild conditions. This timing aligns with heightened nectar-seeking behavior among honeyeaters, when alternative floral resources may be scarce in its southwestern Australian habitat. Secondary pollination by is possible, particularly in areas with reduced activity, though it plays a minor role compared to avian vectors. Genetic studies of natural populations confirm a predominantly outcrossing mating system, with multilocus outcrossing rates (t_m) generally above 0.9, reflecting effective pollen transfer by mobile bird pollinators and low self-compatibility. This outcrossing predominance supports genetic diversity and resilience in remnant populations.

Wildlife interactions

_Hakea laurina provides nectar and pollen as a food source for nectarivorous birds such as honeyeaters and insects including native bees, thereby supporting local biodiversity in its native habitats. The plant's seeds are winged, enabling wind dispersal; they are retained in serotinous fruits that release them en masse following events to facilitate regeneration. In its fire-prone habitat, seeds are protected in serotinous follicles until heat from triggers release, promoting mass on nutrient-enriched post- soil. Additionally, its dense foliage offers shelter for small mammals in environments. Seedlings of H. laurina experience herbivory from native mammals such as western grey kangaroos, though consumption is reduced by in the foliage acting as chemical defenses.

Conservation

Status

Hakea laurina is classified as Vulnerable (VU) on the of , a status assigned in the 2022 assessment. In , its native range, the species is categorized as not threatened under state conservation codes, though it remains subject to ongoing monitoring by the Department of Biodiversity, Conservation and Attractions. The global population comprises fragmented subpopulations estimated at fewer than 10,000 mature individuals (as per the 2022 IUCN assessment). Overall trends indicate a continuing decline primarily attributed to habitat loss, contrasted by stability in certain protected reserves.

Threats and management

Hakea laurina faces several anthropogenic threats in its native southwest Western Australian range, primarily stemming from habitat loss and degradation. Agricultural clearing has fragmented populations, particularly in the and mallee-heath habitats where the species occurs, reducing available sandy and lateritic soils essential for its survival. Road maintenance activities, including verge clearing and infrastructure development, further exacerbate and directly impact roadside populations. Invasive weeds compete with seedlings for resources, while the soil-borne pathogen (dieback) poses a significant risk to species like H. laurina, often spreading via disturbed sites and leading to mortality in infected areas. Altered fire regimes represent a critical due to the species' seeding strategy and lack of , rendering it highly fire-sensitive. As a serotinous , H. laurina relies on infrequent fires (intervals of 10–20 years or longer) to release canopy-stored for ; frequent burns deplete seed banks before maturation, causing failure and potential local extinctions, especially in fire-prone ecosystems like Proteaceous mallee-heath. Short fire intervals, often resulting from human-induced ignitions or practices, have been documented in key habitats, with up to 16% of areas in nearby national parks experiencing three or more fires within 30–34 years. Conservation management for Hakea laurina emphasizes protection within reserves such as Cape Arid National Park and Fitzgerald River National Park, where significant populations are safeguarded from direct clearing and development. Seed banking efforts, coordinated through the Threatened Flora Seed Centre in Perth, have included collections from H. laurina populations since 2005, with duplicates at the Millennium Seed Bank in the UK to support future restoration and research. Translocation programs, including planting in restoration sites like Peniup under the Gondwana Link initiative, aim to bolster fragmented populations using locally sourced seedlings. Recovery strategies prioritize habitat restoration through revegetation, targeted to mitigate competition and spread, and prescribed burning regimes that maintain intervals exceeding the species' 5–10-year juvenile period to ensure viable recruitment.

Cultivation

Propagation

_Hakea laurina is primarily propagated by seed, which is the most reliable method for reproducing the plant artificially. Seeds are contained within woody follicles that require scarification to break dormancy, typically achieved by exposing the pods to heat—such as placing them in an oven at 180°C for 10 minutes or allowing them to dry in the sun—to release the seeds. Alternatively, smoke treatment, mimicking bushfire conditions common in its native habitat, can enhance germination by applying smoke water or aerosol to the seeds, as many Proteaceae species respond to chemical cues from smoke. Collected seeds, ideally 12 months after flowering to ensure maturity, are then sown in a well-drained seed-raising mix of coarse sand and vermiculite, covered lightly, and kept moist but not waterlogged. Germination typically occurs within 14 to 42 days under warm conditions (around 20–25°C), though it may take 2–3 months in some cases, with success rates varying from 40–70% depending on treatment and conditions. Sowing is best done in autumn to allow establishment by spring, with seedlings transplanted once they reach 4–5 cm in height. Propagation from cuttings is possible but less consistent, often yielding variable success rates due to the plant's shallow-rooted nature. Semi-hardwood cuttings of 75–100 are taken during warmer months (late spring to early summer), with the base scraped to expose and dipped in a rooting powder before insertion into a moist, free-draining mix. The lower two-thirds of leaves are removed to reduce , and the cuttings are kept in a humid, shaded environment until roots form, which can take 5–6 weeks or longer. Rooting success is lower than for seeds, often below 50%, making this method suitable mainly for specific clones rather than mass . Grafting is a viable technique for Hakea species, including H. laurina, with established methods reported since 2002 using seedling rootstocks for improved soil tolerance and growth in eastern Australian gardens. As of 2025, commercial grafted hybrids such as Hakea 'Pinball' (H. laurina × H. petiolaris) are available, offering enhanced adaptability to higher humidity and heavier soils. remains experimental, primarily explored for conservation purposes in rare but not routinely applied to H. laurina due to challenges with explant establishment and .

Growing requirements

Hakea laurina thrives in full sun to partial shade, where it develops compact growth and reliable flowering, though may result in sparser form. It prefers well-drained sandy or loamy soils with a range of 5.5 to 7.0, tolerating a variety of substrates including clay as long as drainage is adequate to prevent . H. laurina's cluster roots release carboxylates and acids to mobilize in low-nutrient soils, underscoring the importance of low-phosphorus fertilizers to avoid toxicity (as of 2025 research). Once established, the plant exhibits moderate water needs and strong , requiring occasional in dry periods but avoiding waterlogged conditions. It is frost tolerant to approximately -5°C after establishment, making it suitable for USDA hardiness zones 9–11, and performs well in both coastal and inland gardens with some protection from severe winter winds. Pruning should be light and undertaken after flowering to maintain shape and encourage bushiness, while fertilization must use low-phosphorus formulations specific to native to avoid toxicity common in the family. These conditions mirror its to sandy, low-nutrient habitats in southwestern .

Horticultural uses

_Hakea laurina is valued ornamentally for its striking winter blooms and attractive foliage, featuring rounded, pincushion-like flower heads in or that appear from autumn through late winter, providing color during cooler months. The plant's dense, habit and leathery leaves add year-round structure to landscapes. In , it serves multiple practical roles, including hedging and screening due to its upright growth and compact form, reaching up to 6 meters in height. It is also employed for , leveraging its root system to stabilize soil in sloped or coastal areas. Additionally, its potential as a tree stems from its tolerance to urban conditions and ornamental appeal. The species enhances gardens by attracting nectar-feeding birds and with its profuse blooms, supporting in cultivated settings. Its long-lasting flowers make it suitable for cut flower arrangements, where the unique spherical heads maintain color and form for extended periods. Hakea laurina is cultivated widely in for native gardens, in , , for drought-tolerant landscapes, and in , , for ornamental plantings. Culturally, it holds significance in heritage as "Kodjet," symbolizing resilience, with the hard wood historically used for tool handles. In modern applications, flower essences derived from its blooms are employed for emotional and spiritual healing.

References

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