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Hydrangea macrophylla

Hydrangea macrophylla, commonly known as bigleaf hydrangea, French hydrangea, or mophead hydrangea, is a woody in the family Hydrangeaceae native to . It features large, opposite, oval to rounded leaves up to 20 cm long with serrated edges and a coarse texture, growing in a rounded typically 3-6 feet (1-2 m) tall and wide. The plant produces showy inflorescences in mid- to late summer, consisting of flattened or dome-shaped clusters (corymbs) up to 20 cm across, with flowers that are primarily pink, blue, or white depending on —acidic conditions favor blue hues due to aluminum uptake, while alkaline soils yield pink. There are two main flower types: mopheads with rounded heads of mostly sterile florets for a full, appearance, and lacecaps with flat clusters of small fertile flowers surrounded by larger sterile ones. Widely cultivated as an in temperate gardens worldwide, H. macrophylla is prized for its long-lasting blooms that attract pollinators and provide striking summer color, often used in borders, woodland gardens, and as specimen plants. It thrives in USDA hardiness zones 5-9, preferring partial shade, especially afternoon shade in warmer climates, and consistently moist, well-drained, organically rich soil to prevent . should be done carefully after flowering since most cultivars bloom on old wood, though reblooming varieties flower on both old and new growth, extending the display into fall. Numerous cultivars have been developed, including compact forms and those with enhanced color stability or variegated foliage, making it a versatile choice for modern .

Taxonomy

Etymology and nomenclature

The genus name Hydrangea derives from the Ancient Greek words ὕδωρ (hydōr, meaning "") and ἄγγος (angos or angeîon, meaning "vessel" or "capsule"), alluding to the cup-shaped seed capsules of the plants that can retain . This nomenclature was coined by in 1753, drawing from earlier observations of the fruit structure. The specific epithet macrophylla originates from the Greek μακρός (makros, "large") and φύλλον (phyllon, "leaf"), highlighting the species' characteristic large, broad leaves. Common names for Hydrangea macrophylla include bigleaf hydrangea, French hydrangea, hortensia, and mophead hydrangea, the latter referring to cultivars with rounded flower heads. The name "hortensia" emerged in 18th-century following the plant's introduction from around 1788, when it was initially classified under the genus Hortensia by in 1789, possibly honoring the French name or derived from Latin hortus (garden). This term persists as an old-fashioned descriptor for mophead forms and remains the common name in French and Spanish. The accepted binomial is Hydrangea macrophylla (Thunb.) Ser., with the authority attributed to for the original description as Viburnum macrophyllum in 1784, and Nicolas Charles Seringe transferring it to in 1830 as part of Augustin Pyramus de Candolle's Prodromus Systematis Naturalis Regni Vegetabilis. A notable synonym is Hydrangea hortensis Sm., proposed by James Edward Smith in 1792, which reflects early European naming conventions but is now considered obsolete.

Classification

Hydrangea macrophylla is classified within the kingdom Plantae, phylum Tracheophyta, class Magnoliopsida, order Cornales, family Hydrangeaceae, genus , and species H. macrophylla (Thunb.) Ser.. The species is recognized as a distinct entity in modern , though debates persist regarding its infraspecific divisions, particularly between the mophead (var. macrophylla) and lacecap (var. normalis) forms based on architecture. Some classifications treat these as varieties, while others recognize them as forms (f. macrophylla and f. normalis), reflecting ongoing discussions on their genetic and morphological distinctiveness. Close relatives include H. serrata, often grouped with H. macrophylla in phylogenetic analyses due to shared East Asian origins and genetic similarities, and H. quercifolia, a North American species representing broader disjunct distributions in the genus. Phylogenetic studies place H. macrophylla within Hydrangea Macrophyllae, with the Hydrangeeae showing an Asian origin and divergence around million years ago, calibrated using fossil evidence from the .

Description

Morphology

Hydrangea macrophylla is a characterized by a rounded to spreading growth habit, typically reaching 1 to 3 meters (3 to 10 feet) in height and width, with multi-stemmed shoots emerging freely from the base. The plant exhibits a coarse texture and fast growth rate, forming a bulky structure that can vary in overall size depending on the , though the species typically maintains this moderate stature under optimal conditions. The leaves are , , and ovate to obovate or elliptic in , measuring 10 to 20 centimeters (4 to 8 inches) in length and 5 to 13 centimeters (2 to 5 inches) in width, with serrated margins, a rounded base, and an acuminate tip. They are glossy dark green on the upper surface, thick-textured, and essentially glabrous or slightly felted on the lower surface, supported by petioles 2.5 to 7.5 centimeters (1 to 3 inches) long; in autumn, the foliage often turns yellow before abscising. Stems are woody and emerge directly from the ground with limited branching, featuring light brown to tan coloration, large leaf scars, and shreddy, peeling on older growth. New shoots are pubescent, contributing to the plant's textured appearance during active growth. The is fibrous and shallow, spreading widely to facilitate efficient uptake of from the upper layers. Inflorescences vary by form, with mophead types featuring rounded clusters dominated by showy sterile florets and lacecap types displaying flatter corymbs with central fertile flowers surrounded by sterile ones.

Flowering and fruit

Hydrangea macrophylla produces terminal in the form of corymbs, typically measuring 10-20 cm across, with pubescent branches supporting both fertile and sterile flowers. The species exhibits two primary inflorescence types: mophead, characterized by rounded clusters dominated by enlarged sterile florets that create a dome-shaped appearance, and lacecap, featuring a central cluster of small fertile florets surrounded by a ring of larger sterile florets along the margins. Individual flowers are actinomorphic. Fertile flowers measure 4-6 mm in diameter, with deltate sepals 0.5-1 mm long, five ovate petals 1-2 mm long, eight to ten stamens, and an inferior, 2-5-locular . Sterile florets lack true petals and instead possess four prominent, petaloid sepals that are ovate to orbicular in shape and can reach 2-5 cm across. Following , the plant develops dry, dehiscent capsules as , which are small, narrow, and oval, approximately 6-8 mm long, containing numerous minute, dust-like seeds that are to and longitudinally striate. These capsules turn brown and persist on the plant, with occurring in autumn as the capsules dehisce. In temperate climates, blooming typically initiates in and extends through , with the duration influenced by and environmental conditions. Certain reblooming cultivars, such as those in the series, exhibit additional flowering on new growth later in the summer, potentially extending the bloom period until the first frost.

Distribution and habitat

Native distribution

Hydrangea macrophylla is endemic to and occurs naturally in the temperate regions of south-central , particularly coastal areas on the Pacific side such as the Miura and Boso peninsulas, as well as the and Ogasawara (. The species inhabits coastal areas, including s, forest margins, and grasslands near the , often in moist, shaded environments such as woodlands, forest edges, and stream banks at elevations from up to approximately 1000 meters. It prefers acidic to neutral soils rich in that retain moisture, thriving in well-drained conditions. The native climate for H. macrophylla features cool, humid summers and mild winters, corresponding to USDA hardiness zones 6 to 9, with high annual rainfall that supports its growth in these humid, temperate settings. Its historical range has shown stability, remaining confined to these locales without evidence of significant natural expansion beyond its endemic areas prior to .

Introduced ranges

_Hydrangea macrophylla was first introduced to in the late 18th century, with specimens arriving in around 1788 via English surgeon Alexander Duncan, who collected plants during his time in China. Subsequent introductions from in the 1820s and 1830s, facilitated by botanist , brought additional cultivars that popularized the species in European gardens. By the , the plant had spread to , likely through colonial trade routes in the early 1800s, and later to and during colonial expansion, where it became a staple ornamental . Today, it is widely cultivated across these continents for its ornamental value in gardens and landscapes. The species thrives in USDA hardiness zones 5 to 9, preferring temperate climates with consistent humidity and moderate temperatures. It performs best in regions such as the , where ample rainfall supports its moisture needs, and coastal areas of , including the and Mediterranean fringes, benefiting from mild winters and foggy conditions. In and , cultivation is concentrated in cooler, wetter southern and coastal zones, mirroring its native habitat requirements for partial shade and well-drained, acidic to neutral soils. Outside its native range, H. macrophylla has occasionally naturalized and exhibits potential invasiveness in suitable habitats, particularly moist, shaded woodlands and forest edges. In , it is classified as an environmental weed, spreading via birds and water in high-rainfall areas like the , where it competes with native understory plants for light and resources, though its impact remains localized. In the , spontaneous populations have been documented in states like and , arising from discarded horticultural material, but it is not considered aggressively invasive, forming small thickets in disturbed, humid sites without widespread displacement of natives. Overall, its is limited compared to more aggressive ornamentals, due to reliance on human-assisted dispersal. Adaptation to arid or extreme climates poses significant challenges for H. macrophylla, as it demands high and is sensitive to stress, leading to , reduced flowering, and dieback in dry regions without supplemental . In hot, arid areas like inland or the , plants struggle with excessive and heat, often requiring shaded microclimates and mulching to survive, though long-term establishment is rare. Similarly, in colder extremes beyond zone 5, late frosts damage flower buds, limiting bloom reliability, while intense summer heat in climates exacerbates water loss from its large leaves. These limitations confine successful cultivation to humid, temperate zones globally.

Ecology

Pollination and reproduction

Hydrangea macrophylla exhibits primarily entomophilous pollination, facilitated by such as , , and hoverflies that visit the fertile florets within its inflorescences. The species features two flower types: small, fertile florets that produce and , and larger, sterile florets that enhance visual attraction to without contributing to production. This dimorphic structure ensures pollinator access to rewarding fertile flowers, though many cultivated varieties emphasize sterile florets, thereby reducing overall set while maintaining appeal to . Reproduction in H. macrophylla occurs through both and means, with being predominant in natural populations but limited in cultivation. The species is strongly self-incompatible, preventing successful and promoting via pollen transfer from compatible individuals, as evidenced by reduced growth in self-pollinations compared to cross-pollinations. yields from fertilized ovules within dehiscent capsules, which open in late summer to release numerous small, dust-like dispersed by ; however, seed viability is generally low in wild settings due to factors like mismatches in interpopulation crosses and environmental constraints. supplements seed-based propagation through natural processes like of low-lying stems that root upon contact with , allowing clonal spread in suitable habitats. In ecosystems, particularly in introduced ranges, H. macrophylla supports native pollinators by providing seasonal and resources during its summer blooming period, contributing to biodiversity despite its non-native status in many regions. However, in some introduced regions like the and , it has become invasive, potentially displacing native flora. The structure briefly influences pollinator access by positioning fertile flowers centrally or peripherally, optimizing visitation efficiency.

Pests and diseases

Hydrangea macrophylla faces several biotic threats from pests, fungal pathogens, , and occasionally viruses, which can lead to reduced vigor, aesthetic damage, and plant decline in both native Asian habitats and introduced regions worldwide. These issues are more pronounced in cultivated settings where environmental stress exacerbates susceptibility, such as or poor that weakens plant defenses. Management typically relies on cultural practices like proper spacing for air circulation and to remove infected debris, though chemical interventions may be necessary for severe infestations. Among insect pests, (family ) are common sap-feeders that cluster on new growth, causing leaf curling, distortion, and stunted shoots through injection of saliva that disrupts plant tissues. Their feeding also produces sticky honeydew, promoting growth on leaf surfaces. reproduce asexually via , with females giving birth to live nymphs that mature in 7-10 days under warm conditions, enabling rapid population explosions of up to 12 generations per year. Spider mites, particularly the two-spotted spider mite (Tetranychus urticae), use piercing-sucking mouthparts to extract cell contents, resulting in stippled, bronzed, or yellowed leaves and fine webbing on undersides; severe infestations defoliate plants. Their —from to —spans 5-20 days depending on and , with multiple overlapping generations in hot, dry summers. Scale insects, such as oystershell scale (Lepidosaphes ulmi), appear as small, immobile bumps on stems and leaves, sucking and causing yellowing, wilting, and ; armored scales protect themselves with waxy coverings, while their crawlers (mobile juveniles) spread via wind or tools, maturing in 1-3 months. Rose chafers (Macrodactylus subspinosus), beetles, chew ragged holes in flowers and foliage during summer, preferring sunny exposures; their one-year involves larval root-feeding in soil followed by emergence in June-July for 2-4 weeks of feeding. Fungal diseases pose significant risks, especially in humid environments. Powdery mildew (Erysiphe polygoni) manifests as a white, powdery coating on upper leaf surfaces, leading to chlorosis, premature leaf drop, and weakened growth; spores spread via wind, thriving in moderate temperatures (60-80°F) with high humidity but dry foliage. Leaf spot diseases, caused by fungi like Cercospora hydrangeae, produce circular brown spots with yellow halos on leaves, often coalescing to cause defoliation; infections start in wet springs, with spores overwintering on debris. Botrytis blight, or gray mold (Botrytis cinerea), affects flowers and buds, turning petals brown and developing fuzzy gray spores, particularly after prolonged wetness; the pathogen persists as sclerotia in soil or plant parts. Root rot, commonly from Phytophthora species like P. cinnamomi, occurs in waterlogged soils, causing wilting, root decay, and sudden collapse; oospores survive in soil for years, infecting via wounded roots in cool, wet conditions. Bacterial diseases include and wilt from pathogens like Xanthomonas campestris pv. hydrangeae, which enter through wounds or stomata, producing water-soaked spots that turn necrotic and lead to vascular blockage and wilting; symptoms worsen with overhead watering that splashes . Viral infections are rare but can include hydrangea ringspot virus, causing faint ring patterns and mottling on leaves without systemic spread; transmission occurs via contaminated tools or , with no cure and emphasis on rogueing affected . In native Japanese forests, H. macrophylla encounters fewer novel pests due to co-evolved resistances, whereas in introduced ranges like , local insects and pathogens adapt more readily, increasing outbreak risks. Stressed plants, such as those in compacted or nutrient-poor soils, show heightened vulnerability to these threats, as reduced vigor impairs natural defenses like stomatal closure or chemical repellents.

Physiology and chemistry

Flower color variation

The flower color of Hydrangea macrophylla varies prominently based on , with blooms appearing pink or red in alkaline conditions (pH greater than 6.5) and in strongly acidic conditions (pH less than 5.5); or hues occur in intermediate pH ranges (5.5–6.5). White or green hues occur in certain cultivars that remain unaffected by pH changes. These variations stem from the underlying pigment , which shifts appearance depending on environmental factors. Color changes are observed primarily in mophead (hortensia) and select lacecap forms where the sepals produce anthocyanins, enabling the pH-responsive pigmentation; fertile flower colors in the center remain stable and unaffected. Once established during sepal development, the color is generally stable for the bloom's duration, though gradual shifts can occur across seasons if soil conditions alter before flowering. The pH-dependent color variation in H. macrophylla was first noted in during the early . The role of as the primary driver through its influence on aluminum availability was elucidated in –1940s. Gardeners commonly manipulate these colors for aesthetic purposes by amending : adding raises to promote pink tones, while incorporating or aluminum sulfate lowers acidity to achieve blue shades.

Biochemical mechanisms

The primary pigment responsible for sepal coloration in Hydrangea macrophylla is the delphinidin-3-glucoside, which exists in a blue form in but undergoes structural modifications that alter its visible hue depending on environmental and physiological factors. This pigment accumulates in the vacuoles of epidermal cells, where its color is influenced by interactions with metal ions and other molecules. The formation of the blue hue involves complexation between delphinidin-3-glucoside and aluminum ions (Al³⁺), which occurs under acidic conditions. In soil with a of 5.2–5.5, Al³⁺ becomes solubilized and is taken up by the plant roots, subsequently transported to the sepals and binding to the within vacuoles to form a stable metalloanthocyanin complex. In contrast, alkaline soil conditions ( above 6.0) cause Al³⁺ to precipitate as insoluble hydroxides, preventing uptake and complex formation; here, the relies on co-pigmentation with flavones and other , resulting in a pink coloration due to bathochromic shifts and stabilization of the flavylium cation form. This Al³⁺-delphinidin complex can be simplified as: \text{delphinidin-3-glucoside} + \text{Al}^{3+} + \text{copigment} \rightleftharpoons \text{blue metalloanthocyanin complex} The binding shifts the pigment's absorption maximum from approximately 520 nm (characteristic of the pink monomeric form) to around 560 nm, enhancing blue visibility through extended conjugation and charge delocalization. The biochemical processes are genetically regulated by structural genes in the anthocyanin biosynthesis pathway, including chalcone synthase (CHS), chalcone isomerase (CHI), flavanone 3-hydroxylase (F3H), dihydroflavonol 4-reductase (DFR), anthocyanidin synthase (ANS), and UDP-glucose:flavonoid 3-O-glucosyltransferase (UFGT), which control pigment production. Aluminum uptake and transport are mediated by specific metal transporters, such as plasma membrane-localized HmPALT and vacuolar HmVALT, enabling selective accumulation in blue-capable cultivars. White-flowered variants arise from mutations or downregulation in these anthocyanin synthesis genes, leading to negligible pigment levels.

Cultivation

History of cultivation

_Hydrangea macrophylla has been cultivated in for centuries prior to the , primarily for its ornamental value in gardens and its use in traditional practices such as amacha, a sweet derived from its leaves, which contain phyllodulcin, a natural non-caloric sweetener. The plant's native habitats in Japan's mountainous regions facilitated early selection for desirable traits like flower color and form, with references to (the Japanese name for ) appearing in poetry and literature as early as the 8th century. This long history of in laid the foundation for its global ornamental appeal. The species was first introduced to in the late 18th century through Dutch traders and botanists associated with the , with providing the initial scientific description in 1784 based on specimens from . Living plants arrived shortly thereafter, with the first viable specimens reaching in 1788 via Sir Joseph Banks, who received them from and ; these were initially known as Hortensia before being renamed Hydrangea macrophylla in 1830. By the 1830s, the plant had gained popularity in and , where breeders began developing color-changing varieties influenced by , leading to the creation of mophead and lacecap forms that became staples in Victorian gardens. Its arrival in the United States occurred around 1800, with early cultivation in Philadelphia-area gardens such as The Woodlands by William Hamilton, who imported European cultivars and adapted them to American landscapes. In the , cultivation advanced significantly with focused breeding efforts for reblooming capabilities and disease resistance, exemplified by the introduction of the Endless Summer in 2004, the first bigleaf hydrangea to reliably flower on both old and new wood, extending its bloom period. Post-World War II economic recovery spurred the growth of commercial cut-flower industries in and , where H. macrophylla became a key crop for greenhouses due to its prolific blooms and vase life. Culturally, H. macrophylla holds symbolic importance, representing apology and heartfelt emotion in , stemming from legends where emperors gifted the flowers to express and . In Victorian , it symbolized gratitude and understanding, often given as a token of appreciation for or support in contexts.

Propagation methods

Hydrangea macrophylla is primarily propagated vegetatively to maintain characteristics, though sexual propagation via seed is possible but less common due to . Vegetative methods such as cuttings, , and ensure true-to-type plants, while is used commercially for large-scale, disease-free production. Cuttings are the most widely used technique for H. macrophylla, with , semi-hardwood, and types employed depending on the season. cuttings, taken from terminal shoots in early summer, are treated with 1,000 ppm (IBA) rooting hormone and root in 3-5 weeks under high humidity with near 100% success. Semi-hardwood cuttings, collected in late summer, involve a basal dip in 500-1,500 ppm potassium salt of IBA (K-IBA) for 5 seconds, achieving reliable rooting under mist. cuttings, harvested in winter from dormant stems, root more slowly but are viable with similar hormone treatments. Layering provides a simple, low-risk method for propagating H. macrophylla in the , particularly for low-branching . Simple or tip involves wounding a flexible , burying the tip in moist , and securing it with a peg or stone; roots typically form in 1-2 months in humid conditions. This technique leverages natural rooting tendencies in moist soils and is effective for establishing new near the parent. Division is suitable for mature H. macrophylla clumps, allowing separation of offsets or suckers to create new plants. Performed in spring or fall, the process entails digging up the clump, carefully dividing the root ball with a sharp tool, and replanting sections with intact roots immediately. This method is straightforward for expanding colonies but is less common than cuttings for commercial production. Seed propagation of H. macrophylla is rarely practiced because it results in high variability, failing to produce true-to-type offspring from cultivars, and requires specific conditions for . Seeds are small and sown on the surface of a moist, well-drained medium without covering, as they need light; cold at 4-5°C for 30-60 days improves rates, which are generally low. No is required in some cases, but success remains inconsistent compared to vegetative methods. Tissue culture, or , is employed commercially to produce virus-free stock of H. macrophylla on a large scale. Explants from shoots are sterilized and cultured on supplemented with cytokinins and auxins, such as benzyladenine and IBA, to induce multiple shoot formation and rooting. This method ensures uniform, disease-free plants and is particularly useful for elite cultivars.

Growing conditions and care

_Hydrangea macrophylla thrives in sites with partial shade, receiving 4 to 6 hours of daily, preferably morning sun followed by afternoon shade to prevent scorch. Plant in locations sheltered from strong winds, which can damage buds and stems, and ensure well-drained yet consistently moist to support . Applying 2 to 3 inches of organic mulch, such as pine bark or , around the base helps retain , suppress weeds, and regulate temperature. The plant prefers fertile, humus-rich loamy soil enriched with for optimal growth. significantly influences flower color: acidic conditions (pH 5.0 to 5.5) promote blue blooms by increasing aluminum availability, while neutral to alkaline soils (pH 6.5 or higher) yield pink flowers; adjust pH using aluminum sulfate to acidify for blue or to raise for pink. Fertilize in spring with a balanced NPK formula, such as 10-10-10, at a rate of about 1 per 100 square feet in , May, and July to support vigorous growth without excessive foliage at the expense of blooms. Watering is crucial, as H. macrophylla is sensitive to ; provide at least 1 inch of water per week through deep soakings to maintain even , especially during hot, dry periods. Avoid overhead to minimize leaf wetness and reduce the risk of fungal diseases like . Pruning should occur immediately after flowering for most cultivars, as they bloom on old wood; remove spent blooms and cut back weak or crossing stems to encourage airflow and future bud formation. In late winter, prune out dead or damaged wood to rejuvenate the plant. Reblooming varieties can tolerate lighter at any time, as they flower on both old and new wood. In USDA hardiness zones 5 and 6, where the plant is marginally hardy, apply an extra layer of over the root zone in late fall to protect against winter dieback, a common issue that can prevent blooming by killing flower buds. Non-reblooming cultivars are particularly susceptible, so in protected areas enhances winter survival.

Uses

Ornamental uses

_Hydrangea macrophylla is widely utilized in garden settings as a versatile , serving as specimen plants to create focal points, in mixed borders for layered interest, as hedges or screens for privacy, and in gardens where its preference for partial shade aligns with natural conditions. Mass plantings of these shrubs deliver striking color impacts through their large inflorescences, while container-grown specimens add ornamental value to patios and urban spaces, allowing for mobility and controlled environments. In floral design, the cut flowers of Hydrangea macrophylla are prized for their showy, globe- or lace-like clusters, which remain attractive in bouquets and arrangements for 7-10 days under optimal vase conditions, though vase life can extend to 15-28 days with preservatives depending on cultivar and harvest stage. Their substantial size and vibrant hues make them a staple in fresh flower compositions, often combined with other blooms for added volume and texture. Landscape designers incorporate Hydrangea macrophylla into color-themed gardens, such as drifts of or pink-flowered varieties to evoke seasonal moods, and pair it with shade-tolerant companions like ferns and hostas to enhance textural contrast in partially shaded borders. The plant provides year-round appeal, with summer-to-fall blooms transitioning to colorful autumn foliage in , , and , contributing sustained visual interest. variations, including mophead and lacecap types, further amplify its ornamental versatility in these designs. Commercially, Hydrangea macrophylla is produced on a large scale through greenhouse forcing techniques, enabling year-round availability for markets in and the , particularly timed for holidays like and via precooled dormant cuttings. This method supports consistent supply to florists and retailers, leveraging the species' responsiveness to controlled temperature and photoperiod manipulations.

Other applications

In traditional Japanese medicine, the leaves of Hydrangea macrophylla have been used to prepare that suppresses pruritus, anaphylactic shock, and allergic responses by inhibiting secretion. The plant's and roots are employed in folk remedies for their purported and effects, attributed in part to compounds like hydrangeic acid, which exhibits anti-diabetic activity by lowering blood glucose, , and free levels. Water extracts of processed H. macrophylla leaves have demonstrated attenuation of pro-inflammatory mediators through suppression of the Akt-mediated pathway, supporting its historical use for reducing . However, H. macrophylla is mildly toxic and contains cyanogenic glycosides; ingestion of large quantities can cause digestive upset such as vomiting and diarrhea, and medicinal use should be approached with caution or under professional guidance. Phytochemical studies highlight the potential properties of anthocyanins derived from H. macrophylla flowers, which contribute to free radical scavenging activities such as , , and inhibition, though clinical evidence for use in health supplements remains limited. Extracts rich in these show promise for applications in nutritional supplements aimed at combating , but further human trials are needed to substantiate efficacy. Ecologically, the of H. macrophylla aids in on slopes and hillsides by stabilizing and preventing runoff, making it suitable for naturalized areas prone to soil loss. In such settings, the plant supports , attracting pollinating to its fertile florets and providing cover and seeds for . Industrial applications include the extraction of natural blue pigments from H. macrophylla sepals, formed by supramolecular complexes of glucosides and metal ions, which have been explored for use in dyes and as stable, eco-friendly colorants. Cellular extracts of the plant are incorporated into cosmetic formulations for their benefits, leveraging the same compounds.

Selected cultivars

Mophead varieties

Mophead varieties of Hydrangea macrophylla are characterized by their large, rounded inflorescences composed primarily of showy, sterile florets that form dense, ball-like clusters typically measuring 15-25 in . These blooms emerge in and can persist into early autumn, creating bold, globular displays that dominate the shrub's rounded , which reaches 1-2 in and width. Unlike lacecap forms, mopheads lack prominent fertile florets at the center, emphasizing instead the uniform, petal-like sterile flowers for ornamental impact. Among the most notable mophead cultivars is '', introduced in 2004 as the first reblooming bigleaf capable of flowering on both old and new wood, producing pink or blue mophead clusters that extend the bloom period from through frost in USDA zones 4-9. Another classic is 'Nikko Blue', a mid-20th-century selection prized for its vibrant blue flowers in acidic soils (pH below 6), forming rounded heads up to 12 across on shrubs growing 1.2-1.8 m tall. 'Big Daddy' stands out for its enormous inflorescences, reaching up to 35 in diameter, with enhanced heat tolerance suited to humid southern climates, where it produces pink or blue blooms on 1.5-1.8 m plants. For smaller gardens, 'Pia' offers a compact form, growing only 0.6-0.9 m tall and wide, with dwarf mophead flowers in pink to purple-red shades measuring about 10 across. Breeding efforts for mophead varieties have emphasized improved color stability through soil pH responsiveness, enhanced disease resistance to common issues like , and the development of repeat-blooming traits to ensure consistent flowering regardless of pruning timing or winter damage. These advancements, often achieved via selective hybridization, allow cultivars to maintain bloom reliability on both established and current-season growth. Mophead varieties dominate commercial horticultural trade due to their eye-catching, full-bodied flower displays, which are widely used in for borders, hedges, and plantings, outselling other H. macrophylla forms for their dramatic visual appeal.

Lacecap varieties

Lacecap varieties of Hydrangea macrophylla feature inflorescences with a central of small, fertile flowers surrounded by a ring of larger, flattened sterile sepals, forming flat-topped heads typically 10-15 cm in diameter that offer a more delicate and naturalistic appearance compared to denser flower forms. These structures closely resemble the wild-type forms native to , where fertile flowers in the center support seed production and attract pollinators. Breeding efforts for lacecap cultivars emphasize enhancing fertility to promote seed set and pollinator appeal, while achieving subtle color variations through manipulation and better integration into garden settings via compact habits and extended bloom times. This focus results in plants that blend seamlessly into naturalistic designs, prioritizing ecological benefits over bold displays. Due to their fertile central flowers, lacecap varieties are particularly popular in wilder landscapes and pollinator gardens, drawing significantly more than sterile-heavy types and supporting in shaded borders or edges. Notable examples include '', a with cascading branches bearing or lacecap blooms featuring wavy outer sepals, reaching up to 2 m tall and wide. 'Lanarth White', a compact heritage selection with the Royal Horticultural Society's , produces elegant pure white lacecap heads up to 150 cm tall, occasionally with mauve- fertile centers for added subtlety. 'Twist-n-Shout', a reblooming variety, displays deep or lacecaps on upright stems with vivid coloration, blooming repeatedly from through fall on plants 1-1.5 m tall.

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