Hypericum aegypticum | |
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Scientific classification | |
Kingdom: | Plantae |
Clade: | Tracheophytes |
Clade: | Angiosperms |
Clade: | Eudicots |
Clade: | Rosids |
Order: | Malpighiales |
Family: | Hypericaceae |
Genus: | Hypericum |
Section: | Hypericum sect. Adenotrias |
Species: | H. aegypticum |
Binomial name | |
Hypericum aegypticum | |
Subspecies | |
Synonyms [1] [2] | |
Hypericum aegypticum is a species of flowering plant of the St. John's wort family (Hypericaceae) which is native to the Eastern Mediterranean. It was described by Carl Linnaeus in the second volume of his Species Plantarum in 1753, who named it after Egypt despite it not being distributed there. The plant is commonly known as shrubby St. John's wort or Egyptian St. John's wort in English. Like other members of section Adenotrias , it is found among limestone rocks in coastal areas. While it has been evaluated as threatened on the island of Malta, the species has no legal protections.
The species is a shrub or shrublet that grows up to 2 meters (6.5 feet) tall with many branches, each having a single small flower with five yellow petals and many stamens. Its leaves lack hairs, and have densely patterned glands and large primary veins. The species is notable for its heterostyly, a trait which within the Hypericum genus is unique to section Adenotrias, and exhibits one of two heterostylous flower types called "pins" and "thrums". It has three subspecies, which vary in their distribution and phytochemical makeup.
Hypericum aegypticum is a shrub or shrublet that varies in height from 0.05 to 2 meters (0.16 to 6.5 feet) tall. It grows in a crowded, spreading pattern, with its stems stretching out from the center of the plant. The branches grow roughly perpendicular from these stems, but can also spread out in different directions. [3] It has a chromosome number of 2n=20. [4] : 334
The stems of Hypericum aegypticum usually have two visible lines running along their length, but can sometimes have four. When the plant is young, the stems are a flatter shape with two edges (ancipitous), but quickly become more cylindrical as the plant matures. [3] In a cross-section, the profile of the stems is circular and lacks wing-like extensions. They have a vessel density of roughly two vessels per square millimeter of stem, with each of these vessels measuring 15 micrometers in diameter. [5] In between the nodes where the leaves branch from (in the internodes), there are small leaf-like structures which are shorter than the true leaves. [3]
The xylem in the stems, a type of transport tissue, differs from other similar species of Hypericum. The xylem of H. aegypticum is diffuse; it is spread evenly throughout the stem. In other similar species, the xylem is ring-porous and more dense in a series of concentric rings. There are two secretory structures in the stems: small secretory canals in the phloem and many large secretory canals in the cortex. [5]
The leaves of Hypericum aegypticum are free and range from sessile to shortly petiolate. They persist for around two seasons. The blades are 3–18 millimeters (0.1–0.7 inches) long and 1–5 millimeters (0.04–0.20 inches) wide. Their shape is elliptic or narrowly oblong. The leaves are the same color as the rest of the plant and have a texture similar to that of leather. The shape of their tip can range from acute to obtuse and the base of the leaf is wedge-shaped. [3] The leaves lack hairs (trichomes) on both the top and bottom. [5]
They have one pair of lateral veins, with the midrib sometimes branched and visible beneath them. [3] Their primary veins are very large and straight and are highly rigid. The secondary veins branch off at acute angles of wide divergence, and some tertiary veins with a branched pattern are also present. [6]
The laminar and marginal glands are dense. [3] Unlike some species of Hypericum, such as H. perforatum , H. aegypticum lacks black nodules on its leaves. Instead, it has small translucent glands which measure 54 by 45 micrometers and are found in the mesophyll. [6]
The upper sides of the leaves have an outer layer (epidermis) made of cells with linear walls and rounded corners. This upper side also has stomata that are surrounded by smaller cells. The lower side of the leaves have a similar composition to the upper side, but with a higher density of stomata. On both sides, there is a cuticle that extends over the entire surface, even over the guard cells, which makes them very hard to distinguish. This thick cuticle leads to increased impermeability in areas where there are encrusted deposits. [5] [7]
Hypericum aegypticum is one-flowered, and its inflorescence is terminal and grows from around four axils below. It has short flowering branches past a "sterile" region which lacks them. These branches grow from around eleven different nodes. However, some plants lack the sterile region and can have flowers or flowering branches from up to twenty-two nodes. The inflorescence is similar in appearance to a spike, with longer branches below the flowering region. The bracts are often absent, but when they are present they are leaf-like in appearance, with a clasping calyx and several types of glands. The pedicels are very short or absent altogether. [3]
The flowers of H. aegypticum range from 5–10 millimeters (0.20–0.39 inches) in diameter. The shape of the buds is a narrow form between an oval and an ellipse which tapers to a rounded point. The sepals are green and are 3.5–5.5 millimeters (0.14–0.22 inches) by 1–2 millimeters (0.04–0.08 inches) in size. They overlap one another and are not quite the same size. Their shape ranges from oblong to elliptic, but they can also be lance-like in form. Their ends can be rounded, pointed, or obtuse. The sepals are hood-like and stand stiffly erect, and have roughly nine unbranched veins with prominent midribs and linear laminar glands. The petals of the flower range from bright yellow to a rather pale shade of yellow. They are 6.5–12 millimeters (0.26–0.47 inches) by 2–3 millimeters (0.08–0.12 inches) in size. They are persistent in fruit and there are roughly twice as many of them as there are sepals. [3]
There are 18–48 stamens per inflorescence, with single fascicles containing 5–10 stamens and double fascicles containing 5–29 stamens. There are united filaments in each fascicle, the longest of which are 6.5 millimeters (0.26 in) in long-styled individuals and 9 millimeters (0.35 in) in short-styled individuals. Some stamen fascicles are sterile and are 0.6–0.7 millimeters (0.02–0.03 inches) long and flat-topped. The ovaries are 0.5–4 millimeters (0.02–0.16 inches) by 0.5–1 millimeter (0.02–0.04 inches) in size and are narrow or very narrow and acute to truncate. [3]
The seed capsule is 5–7 millimeters (0.20–0.28 inches) by 3–3.5 millimeters (0.12–0.14 inches) in size. Its shape is that of a cylindric ellipsoid to a rather broad ellipsoid. It is longer than the sepals, and its valves run longitudinally and have oil tubes. The seeds are dark brown and roughly 1.5 millimeters (0.06 inches) long and lack a longitudinal ridge. The testa have small linear pits or wrinkles, and the elaiosome is often lobed. [3]
Individual plants of Hypericum aegypticum exhibit one of two different sets of characteristics, called distyly. [8] [9] This polymorphism is characterized by two different types of flowers: one has long styles and short stamens (such specimens are called "pins"), the other has short styles and long stamens (such specimens are called "thrums"). [10] In this species, pin flowers produce and receive more pollen grains than thrum flowers. This is unusual, as it does not fit with the expected course of natural selection; plants in the species which produce and receive more pollen would be expected to outcompete those that produce and receive less. [8] While pin flowers are more common in the wild with a ratio of approximately 3 pins to 1 thrum, that difference is only because the gene which codes for the pin is dominant while the thrum is recessive, and the 3:1 ratio is consistent with traits that have no effect on reproduction. [9]
Hypericum sect. Adenotrias is the only section in Hypericum that exhibits heterostyly, and all of its species, including Hypericum aegypticum, are distylous. This trait is thought to have evolved within the genus as opposed to being primitive and is one of the unique characteristics of sect. Adenotrias. [9] : 271 In studies of eleven angiosperm genera which exhibited distyly, all but Hypericum followed a genetic system called the Primula system, in which the "thrum" form was dominant and the "pin" form was recessive. However, for an unknown reason, the opposite appears to be the case for the species of Hypericum. [9] : 272
The phytochemistry of Hypericum aegypticum varies a great deal depending on which subspecies is analyzed. Subspecies aegypticum, maroccanum, and webii are all highly different in their major essential oil components, with only three constituents being found in common in all of the subspecies: spathulenol, caryophyllene oxide, and E-caryophellene. The major constituent of subsp. aegypticum is ishwarane (a sesquiterpene) the major constituent of subsp. maroccanum is caryophyllene, and the major constituent of subsp. webii is pinene. [11] : 303 [12] : 431 These differences in the compounds detected in the species reveal that morphologically different populations of H. aegypticum are also likely to differ phytochemically. [11] : 305 Small amounts of other metabolites are also present in H. aegypticum, including flavonoids (3.95 g/kg), biflavones (1.45 g/kg), acylphloroglucinols (1.15 g/kg), cinnamic acids (0.35 g/kg), and naphtodianthrones (0.05 g/kg). [13]
Essential oil extracts from Hypericum aegypticum subsp. webbii were shown in vitro to have moderate antimicrobial effects against Gram-positive bacteria such as Bacillus subtilis , Enterococcus faecalis , Staphylococcus epidermidis , and Micrococcus luteus . [12] : 427
Hypericum aegypticum can be found frequently in the wild and is indigenous to Malta, Greece, Morocco, Algeria, and Libya. [14] However, its distribution across these countries is unusual because it is highly fragmented into several different population strands. [15] The three subspecies are divided among these strands: H. aegypticum subsp. aegypticum is native to Libya; subsp. maroccanum is native to Morocco and Algeria; subsp. webbii is native to Sardinia, Sicily, Malta, and Greece. [16]
H. aegypticum is found among limestone rocks and scree in valleys of coastal areas. It is found at elevations from sea level to 1600 meters (5250 feet) above sea level. [14] In some habitats, particularly more wind-swept or exposed areas, the species has been observed in much denser, carpet-like growth patterns, sometimes growing to only 20–30 centimetres (8–12 in) tall. However, the species grows best in open, sunny areas free of other plants which could compete with it. [15]
While H. aegypticum has been identified by the Maltese Red Data Book as having a threatened status on Malta, no legal action has been taken for the protection of the species as of 2021. [14]
While Hypericum aegypticum is not widely cultivated, it is present in botanical gardens, including in a greenhouse at the University of Oxford Botanic Garden. [17]
Hypericum aegypticum was first described by Carl Linnaeus in his second volume of Species Plantarum in 1753. He noted the species' Egyptian habitat, its often paired leaves, growing pattern, and the shape of its leaves. [18] However, even though Linnaeus mentioned "Aegypto" and claimed that his type specimen for the species was from Egypt, H. aegypticum is not actually native to Egypt, and the specimen Linnaeus used most likely came from one of the Libyan populations. [1] Today, H. aegypticum is commonly referred to in English as Shrubby St. John's Wort or Egyptian St. John's Wort, while in Malta it is known as Fexfiex tal-irdum. [14]
The species' placement within Hypericum can be summarized as follows: [1]
After the original description by Linnaeus, various botanists identified the plant under different names which are now considered invalid synonyms of the species. [19] Michel Adanson, in his 1763 work establishing the genus Elodes, erroneously described the species Hypericum elodes by relying upon a supposed description by Linnaeus of the species in his 1753 Species Plantarum. However, the name H. elodes did not appear in the 1762 Flora Anglica , and the name that Adanson actually referenced was Hypericum aegypticum. Therefore, his description under the erroneous name H. elodes is considered to be a synonym of H. aegypticum. [4] : 305 Confusion around Elodes continued, but it was eventually restricted to the singular species H. elodes as originally defined by Linnaeus. In the early 19th century, the species of Hypericum were being divided into numerous smaller, new genera by different authors. Antoine Laurent de Jussieu split it into five genera, confusingly including one called Elodea. Édouard Spach contributed his own restrictive genera and placed H. aegypticum first into Triadenia and then Adenotrias. Robert Keller later reduced all of these new genera to sections within Hypericum in 1925, bringing H. aegypticum back into Hypericum within section Adenotrias. [4] : 306
In 1996, British taxonomist Norman Robson published the sixth volume of his comprehensive monograph on the genus Hypericum. [20] : 3–4 In this volume, Robson recognized Linnaeus' original name as correct and maintained H. aegypticum in sect. Adenotrias, incorporating it into his new framework of 36 sections. [3] Adenotrias was established to comprise three species of shrubs found among limestone rocks which vary greatly in appearance. [21] : 186 However, the species of the section were united because they shared the trait of heterostyly. [15]
Molecular phylogenetics has demonstrated that Hypericum aegypticum is most closely related to H. balfourii and H. socotranum of sect. Campylosporus . However, no conclusive evidence was found which would suggest that these similarities would warrant the inclusion of H. aegypticum in sect. Campylosporus. Phylogenetic studies have also found that H. heterophyllum , despite lacking the floral specializations and heterostyly of H. aegypticum, has similar characteristics to the species, especially H. aegypticum subsp. maroccanum. This suggests that H. heterophyllum is a derivative of the species which has lost some of the specializations that are unique to H. aegypticum and sect. Adenotrias. [21] : 186–187
The following subspecies are accepted by Plants of the World Online: [2]
Beyond their separate distributions, the subspecies also vary slightly in appearance. Subsp. maroccanum grows more upright than its counterparts, subsp. webbii is typically taller and larger, and subsp. aegypticum has petals that are somewhat shorter. Additionally, the branches of maroccanum tend to reach upwards, while aegypticum usually forms a lower bush. Lastly, the leaves of maroccanum are markedly larger than aegypticum or webbii. [1]
Subspecies maroccanum was originally described as a variety of H. aegypticum by Carlos Pau in 1932, while subsp. webbii was originally considered to be its own species under the name Triadenia webbii by Édouard Spach in 1836. Norman Robson reclassified both as subspecies of H. aegypticum in 1993, and established subsp. aegypticum to denote any specimens which were separate from both maroccanum and webbii. [22] : 68
Hypericum perforatum, commonly known as St John's wort, is a flowering plant in the family Hypericaceae. It is a perennial plant that grows up to one meter tall, with many yellow flowers that have clearly visible black glands around their edges, long stamens, and three pistils. Probably a hybrid between the closely related H. attenuatum and H. maculatum that originated in Siberia, the species is now found worldwide. It is native to temperate regions across Eurasia and North Africa, and has been introduced to East Asia, Australia, New Zealand, and parts of North and South America. In many areas where it is not native, H. perforatum is considered a noxious weed. It densely covers open areas to the exclusion of native plants, and is poor grazing material. As such, methods for biocontrol have been introduced in an attempt to slow or reverse the spread of the species.
Hypericum is a genus of flowering plants in the family Hypericaceae. The genus has a nearly worldwide distribution, missing only from tropical lowlands, deserts and polar regions. Many Hypericum species are regarded as invasive species and noxious weeds. All members of the genus may be referred to as St. John's wort, and some are known as goatweed. The white or pink flowered marsh St. John's worts of North America and eastern Asia are generally accepted as belonging to the separate genus TriadenumRaf.
Hypericum mutilum is a species of St. John's wort known by the common name dwarf St. John's wort. It is native to parts of North America and is present in other parts as an introduced species. It is an annual or perennial herb taking a multibranched erect form up to about 60 centimeters tall. The oval green leaves are one or two centimeters long and are covered in tiny glands. The inflorescence is a compound cyme of tiny flowers. H. mutilum subsp. mutilum and subsp. boreale have a diploid number of 16, and H. mutilum subsp. boreale can have a diploid number of 18.
Hypericum annulatum is a species of flowering plant in the family Hypericaceae. It is a perennial herb of varying heights which grows upright, with more than a hundred flowers of a golden yellow color. First described in 1827, the species has a wide distribution from Eastern Europe to East Africa, and its appearance can vary greatly based on its geographic location. It has been used in Bulgarian folk medicine, and has more recently been investigated for its effectiveness in slowing the growth of or killing certain types of human cancer.
Hypericum hircinum is a species of perennial flowering plant in the St John's wort family, Hypericaceae. It is known as goat St John's wort and stinking tutsan; both names refer to the plant's distinctive odor. The species is a bushy shrub that can grow up to 1.5 meters tall, is many-stemmed, and has golden yellow flowers with conspicuous stamens. The plant has been well-documented in botanical literature, with mentions dating back to at least 1627. Carl Linnaeus described H. hircinum several times, including in his 1753 Species Plantarum which established its binomial. At one point the plant was placed into the defunct genus Androsaemum, but it was returned to Hypericum by Norman Robson in 1985.
Adenotrias is a section of flowering plants in the family Hypericaceae. It is made up of Hypericum aciferum, H. aegypticum, and H. russeggeri. When it was first described, it was considered its own independent genus, but was later placed under Hypericum and demoted to a section. Its Latin name Adenotrias is made of the Greek prefix adeno- and the Latin word trias. Species in the section are shrubs up to 2 metres (6.6 ft) tall with smooth leaves and bark, and are the only species in Hypericum with heterostylous flowers. They are found around the Mediterranean coast, with H. aciferum restricted to the island of Crete and H. russeggeri present only in parts of Turkey and Syria. Plants of the section have a habitat among limestone and other calcareous rocks. While H. aegypticum has a wide and generally secure distribution, H. aciferum has been evaluated as endangered since the 1980s, but is now protected in part by a plant micro-reserve near Agia Roumeli.
Hypericum sect. Adenosepalum is one of 36 sections in the genus Hypericum. Its type species is Hypericum montanum.
Hypericum phellos is a species of shrub or small tree in Hypericumsect. Brathys. The species is found in Colombia and Venezuela on scrubby slopes and moist woods.
Hypericum majus, the greater Canadian St. John's wort, is a perennial herb native to North America. The specific epithet majus means "larger". The plant has a diploid number of 16.
Hypericum lancasteri, known as Lancaster's St. John's wort or as zhan e jin si tao in Chinese, is a species of flowering plant in the St. John's wort family Hypericaceae. The species has been awarded the Royal Horticultural Society's Award of Garden Merit.
Hypericum huber-morathii is a species of flowering plant in the St John's wort family Hypericaceae. It is a small perennial herb with few stems. It has narrow and brittle stems, thick leaves, flowers in clusters of varying numbers, small yellow petals, around twenty stamens, and three styles. H. huber-morathii is closely related to H. minutum and H. sechmenii, and also shares characteristics with H. lanuginosum. The plant is endemic to Turkey, and is found among limestone rocks in a limited region of southwestern Anatolia. Originally excluded from a comprehensive monograph of Hypericum, the species' placement within the genus is unclear. It has been placed in both section Adenosepalum and section Origanifolium.
Hypericum aucheri, also known as Koramanotu in Turkish, is a herbaceous perennial flowering plant in the St. John's wort family Hypericaceae.
Hypericum aciferum is a species of flowering plant in the St John's wort family Hypericaceae. It is a small shrub endemic to the Greek island of Crete. H. aciferum grows in a mat on the ground and has twisting branches, needle-like leaves, and long golden petals. Its flowers are also heterostylous, which means that the species can exhibit one of two flower types on different plants. This trait is unique within the genus Hypericum to H. aciferum, H. russeggeri, and H. aegypticum, the three species in section Adenotrias.
Hypericum russeggeri is a species of flowering plant in the St John's wort family Hypericaceae. The plant is a small shrub with many branches that spread across the ground, and it has many small flowers with pale yellow petals. It is found only among calcareous rocks along the coast and in the foothills of the Nur Mountains of eastern Turkey and northern Syria. While H. russeggeri has an array of phytochemicals present in its flowering structures and leaves, these are found in lower concentrations than other species of Hypericum. The species was first described in 1842 as Triadenia russeggeri, and it has been placed into various defunct genera including Elodea and Adenotrias. It is now known as Hypericum russeggeri and is the type species of Hypericum section Adenotrias, a small section that also includes H. aegypticum and H. aciferum.
Hypericum coris, the heath-leaved St. John's wort, also called yellow coris, is a species of flowering plant in the family Hypericaceae, and is the type species of sect. Coridium. It is a low shrub, and it is found in Switzerland and northwestern Italy. The species has been a popular garden plant since the 18th century, valued for its long flowering period and for how well it adapts to cultivation.
Hypericum heterophyllum is a flowering plant in the Hypericaceae family and is the only species in Hypericum sect. Heterophylla.
Hypericum elodeoides, commonly called the Himalayan St. John's Wort, is a species of flowering plant of the St. John's wort family (Hypericaceae).
Hypericum orientale, the Ptarmic-leafed St. John's wort or Eastern St. John's wort, is a flowering plant in the family Hypericaceae. It is distributed across northern Turkey, Georgia, the Caucasus, and Dagestan. The species can be found on stony sloped amidst volcanic rocks in the mountains and in light woodlands at elevations of up to 2,300 m (7,500 ft). It flowers from May to June and July to August. The plant has small, bright yellow flowers and grows across the ground in a creeping pattern. It prefers full sun and is ideal for rock gardens, and is hardy down to -30°F.
Hypericum hirtellum is a species of flowering plant in the family Hypericaceae. It is native to Iran and Iraq and is found on chalky, sandy soil at elevations of 300–2,000 meters.