Hellebores: A Comprehensive Guide - Hardcover

Hellebore Morphology

Who could fail to be smitten with hellebores? Anyone with an appreciation of beauty is quickly seduced. Hellebores seem to cast a spell from which you never awaken. Is it the flowers? They lack cloying fragrance to draw you in. Many are small and subtly colored. Even the most colorful fall short of riveting or festive. What can it be? Their precocious nature is part of their allure, but what makes them so much more than alluring? For many, hellebores are an obsession. What other flower, save for cousin Adonis, punches through the ground with flowers open while frost and snow surround them? Like most early bloomers, Adonis is fleeting. Not hellebores; they bloom for two months or more — longer where spring arrives slowly and nights stay cool. Their rich green foliage provides summer and winter structure. For us, they are the whole package — fantastic foliage, precocious bloom, and beautiful flowers. In short, elegant simplicity.

Most hellebores are native to mountainous regions of Europe, in open oak and beech woodlands, scrub, grassy meadows, and on rocky slopes. These areas are characterized by limestone bedrock and calcareous, humus-rich soils. Western Europe, including the British Isles, is home to three species. The odd plant out is Helleborus thibetanus, which is native to China, well outside of the epicenter of hellebore distribution. The rest of the species fall in between, with the bulk of them centered in the Balkan region of the former Yugoslavia. In all aspects, the plants are both charming and beautiful. In their native lands, few species but the Christmas rose (H. niger) are grown in gardens. This wildling is often found in churchyards due its association with the birth of Christ. Today, we value the wild species for their delicate beauty in woodland and informal settings. (Refer to Chapter 3 for more information on species and their distributions.) The hybrids are by far the most popular garden hellebores worldwide, cherished for their early bloom, showy flowers, and decorative evergreen foliage.

Flowers

Hellebore flowers lack conspicuous petals. Five petal-like sepals create the show, a characteristic shared by most members of the buttercup family (Ranunculaceae). Relatives such as buttercups (Ranunculus), windflowers (Anemone), and winter aconite (Eranthis) share the open, cup-shaped flower. Inside the five showy sepals hides a ring of up to 32 subtle petals, modified into tubular or funnel-form nectaries. The center of the flower sports two to ten pistils surrounded by multiple rings of up to 125 stamens. The ovaries, or carpels, of the flower are an essential characteristic for distinguishing certain species. Some carpels are fused at the base, while others are free. After pollination, the sepals of most species fade to rose or green and often persist in an attractive state until the seed is ripe.

Occasionally, double flowers occur in the wild as a result of spontaneous mutation. Doubling is known to occur in H. dumetorum, H. niger, H. orientalis, and H. torquatus. Doubling occurs when the nectaries, which are actually modified petals, become petaloid, or petal-like. In the place of the tubular nectaries, flattened petals are produced inside the ring of fi ve sepals. The effect can be quite attractive.

Sexually speaking, hellebore flowers are protogynus, which means the stigmas are receptive before the stamens in the same flower shed their pollen. This adaptation generally keeps a flower from fertilizing itself and encourages cross-fertilization. Honey bees (Apis mellifera), bumble bees (Bombus spp.), and other small bees are the primary pollinators of hellebores. They visit the flowers quite freely and move pollen throughout the garden. The flowers can be self-fertile, however, and the pollen from a single flower can fertilize the same flower if the stigma is still receptive. More commonly in nature, pollen from one flower fertilizes another flower on the same plant. This is, in fact, a common occurrence in our gardens, though cross-fertilization from one plant to the next also occurs freely.

Flowers are borne clustered at the tips of persistent, leafy aerial stems or on ephemeral flowering scapes with leaflike bracts. The flowers are carried singly (occasionally doubled), as is common in H. niger, or in clusters of three or more. The flowers emerge in winter or early spring, before the new leaves in most species. True leaves are borne on long petioles. After the seeds ripen, the flowering stems do not bloom again.

Fruits and Seeds

The fruit of a hellebore consists of a cluster of dry follicles surrounded by persistent sepals. Follicles split along one inward-facing seam to release the dark brown or black seeds, which are ovoid and sometimes flattened on two sides so they stack neatly in their vessels. The seeds of some species possess fleshy arils called elaiosomes, which encourage ants to distribute them. This dispersal mechanism is called myrmecochory. Sex pheromone mimics are exuded by the eliasomes to lure ants to the ripe seeds. The plants win because the seeds are taken away from the parent, and with less competition they have a better chance of survival. The ant, for its part, gets some fats and starch from the elaiosome — not a bad deal for all involved.

Hellebore seeds experience a combination of endogenous dormancies. This means that when the seed is released from the follicles, the embryo must undergo morphological and physiological changes before it can germinate. The embryo within the seed is immature or not fully developed at the time of dispersal in early summer. The underdeveloped embryo matures as the seed ripens. A chemical inhibitor further suppresses germination. This kind of dormancy is called physiological inhibition. Once the embryo is fully developed and the hormones that inhibit germination are turned off by chilling, a process called cold stratification, the seed is ready to germinate. Most fresh hellebore seed germinates after a warm ripening period followed by modest chilling for 60 to 120 days.

First to emerge as the seed germinates is the radicle (seed root), which penetrates surprisingly deep in a short time. Two untoothed cotyledons (seed leaves) emerge next, and soon after them the first true leaf, which is divided in most species. Of course, there are exceptions. Helleborus vesicarius exhibits a more complex dormancy and forms only cotyledons the first season. After a second chilling, the shoot and first true leaves emerge. Helleborus thibetanus is also a maverick. The cotyledons never emerge from the seed. Instead, a single three-parted leaf emerges straight from the germinating seed. Most hellebores flower within two to four years of germination. (See Chapter 7 for more details.)

Stems and Leaves

The prevailing convention is to divide hellebores into two groups based on whether or not the plants produce persistent aboveground stems. The terms used for describing the two different growth forms are acaulescent, or stemless, and caulescent, or stemmed. The majority of species are considered acaulescent, the stem being entirely underground and represented by a rhizome. Caulescent species bear persistent aboveground stems with distinct leaves borne up the stem. The flowers of caulescent species are borne at the apex of year-old stems. After flowering, the old stems die, and new stems emerge from the crown that bear flowers the following year. The succulent nature of the stems makes them susceptible to winter damage. As a result, they are far less hardy than their acaulescent relatives.

In reviewing the taxonomy and anatomy of the genus Helleborus, Will McLewin (of Phedar Research and...