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Rhododendron ponticum

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(Redirected from Common rhododendron) Species of flowering plant in the heath family Ericaceae This article is about Rhododendron ponticum. For Azalea pontica, see Rhododendron luteum.

Rhododendron ponticum
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Clade: Asterids
Order: Ericales
Family: Ericaceae
Genus: Rhododendron
Species: R. ponticum
Binomial name
Rhododendron ponticum
L.
Synonyms
List
    • Azalea arborea L.
    • Azalea lancifolia (Moench) Kuntze
    • Hymenanthes pontica (L.) H.F.Copel.
    • Rhododendron adansonii E.-A.Baumann
    • Rhododendron catesbaei J.Forbes
    • Rhododendron catesbaeum Dum.Cours.
    • Rhododendron deciduum Andrews ex Steud.
    • Rhododendron hyacinthiflorum Steud.
    • Rhododendron lancifolium Moench
    • Rhododendron lowei Loudon
    • Rhododendron obtusum P.Watson
    • Rhododendron odoratum Lodd. ex Steud.
    • Rhododendron ponticum f. angustilobum Rukhadze & Pachulia
    • Rhododendron ponticum f. aurantiacomaculatum Rukhadze & Pachulia
    • Rhododendron ponticum f. brachystamineum Rukhadze & Pachulia
    • Rhododendron ponticum f. crispatum Rukhadze & Pachulia
    • Rhododendron ponticum f. luteomaculatum Rukhadze & Pachulia
    • Rhododendron ponticum var. obtusum (P.Watson) G.Don
    • Rhododendron ponticum f. parviflorum Rukhadze & Pachulia
    • Rhododendron speciosum Salisb.
R. ponticum flower

Rhododendron ponticum, called common rhododendron or pontic rhododendron, is a species of flowering plant in the Rhododendron genus of the heath family Ericaceae. It is native to the Iberian Peninsula in southwest Europe and the Caucasus region in northern West Asia.

Description

R. ponticum is a dense, suckering shrub or small tree growing to 5 m (16 ft) tall, rarely 8 m (26 ft). The leaves are evergreen, 6 to 18 cm (2.4 to 7.1 in) long and 2 to 5 cm (0.79 to 1.97 in) wide. The flowers are 3.5 to 5 cm (1.4 to 2.0 in) in diameter, violet-purple, often with small greenish-yellow spots or streaks. The fruit is a dry capsule 1.5 to 2.5 cm (0.59 to 0.98 in) long, containing numerous small seeds.

It has two subspecies:

Image Name Distribution
R. p. baeticum (Boiss. & Reut.) Hand.-Mazz. Found in central and southern Portugal and southern Spain (in the Province of Cádiz).
R. p. ponticum Found around the southern Black Sea Basin (eastern Bulgaria, northern Turkey, Georgia, Northern Caucasus) and central Lebanon.

And a variegated variety:

  • R. p. var. heterophyllum R. Ansin – Found in Turkey.

Distribution and habitat

The species has two disjunct populations, one in the southwestern Iberian Peninsula (central and southern Portugal and southwestern Spain) and the other near the southern Black Sea Basin (eastern Bulgaria, northern Turkey, Georgia, and Northern Caucasus). It has also been introduced to Madeira, Myanmar, Belgium, the British Isles, Netherlands and France.

The range in the Iberian Peninsula is limited to mountain ranges, the Caramulo mountains, the Monchique range and the Aljibe range. A remnant of the original laurissilva forests that covered the peninsula 66 million years ago.

Though the common rhododendron was present in Great Britain prior to the most recent ice age, it did not recolonise afterwards and the modern ecology of the island developed without it. Its presence today in Great Britain is due to humans introducing it, and it easily naturalises and becomes a pest in some situations, often covering whole hillsides (especially in Snowdonia and the western Scotland). In the British Isles, it colonises moorlands, uplands, shady woodlands (alongside escaped laurels and the native holly) and in areas of acid soils.

Historical range

Fossil evidence shows it had a much wider range across most of southern and western Europe before the Late Glacial Maximum, or until about 20,000 years ago.

It was noted by the botanist Joseph Pitton de Tournefort during his travels in the Near East in 1700–02, and so received its name from Linnaeus to identify the ancient kingdom on the south shores of the Black Sea, Pontus, in which it grew. At the other end of its range, in southern Spain, Linnaeus' friend and correspondent Clas Alströmer found it growing with oleander. It was introduced to Britain as an ornamental shrub in 1763, and later planted as cover for game birds. It is now considered to be an invasive species.

Cultivation and uses

Closeup of Rhododendron ponticum

Rhododendron ponticum subsp. baeticum is one of the most extensively cultivated rhododendrons in western Europe. It is used as an ornamental plant in its own right, and more frequently as a rootstock onto which other more attractive rhododendrons are grafted. The plants were first grown in Britain in the 1760s, supplied by Conrad Loddiges, and became widely distributed through the commercial nursery trade in the late 18th and early 19th centuries. The roots readily send up suckers from below the graft, often allowing it to overtake the intended grafted rhododendron.

Honey produced with pollen from the flowers of this plant can be quite poisonous, causing severe hypotension and bradycardia in humans if consumed in sufficient quantities, and is known as mad honey due to toxic diterpenes (grayanotoxins). This poisonous honey plays a significant part in the 2023 film A Haunting in Venice.

Sap from a freshly cut branch can be used to treat toothaches.

Invasive species

Suckering of the root, together with its abundant seed production, has led to it becoming an invasive species over much of western Europe and in parts of New Zealand. Rhododendron control is a key element in nature conservation in those areas. Conservation organisations in Britain now believe R. ponticum has become "a severe problem" in the native Atlantic oakwoods of the west highlands of Scotland and in Wales and Ireland, and on heathlands in southern England, crowding out the native flora. Clearance strategies have been developed, including the flailing and cutting down of plants with follow-up herbicide spraying. Injection of herbicide into individual plants has been found to be more precise and effective.

A study in the journal Functional Ecology also showed that invasive rhododendron nectar was toxic to European honeybees (Apis mellifera), killing individuals within hours of consumption. It also paralyzed bees of the species Andrena carantonica, a solitary mining bee. Bees became paralysed and exhibited excessive grooming or other distress behaviours after feeding on Rhododendron nectar, and ate less food than bees fed a control nectar. In contrast the buff-tailed bumblebee (Bombus terrestris) was not affected by the rhododendron nectar. It is important not to see Rhododendron as a problem species for honey bees as they actually avoid the flowers owing to their ability to detect the toxin nectar. The toxicity is caused by grayanotoxin 1 which is one of several highly hydroxylated diterpenoid defence chemicals produced in the leaves of Rhododendron to protect against herbivores – e.g. the Thrips Heliothrips haemorrhoidalis. Some species of honey bee (Apis mellifera sub spp caucasica) tolerate the toxin and make so-called "mad honey".

Identification difficulties

Recent efforts to manage the spread of Rhododendron ponticum in the United Kingdom has led to some controversy, particularly within the grounds of Taymouth Castle in highland Perthshire. There remains debate over appropriate identification of the plant, particularly where it is interspersed amongst clumps of Japanese laurel (Aucuba japonica) in areas of mixed woodland. Tensions surrounding the management of these cohabiting species were brought to a head in early December 2022 when prominent arboriculturalists faced strong opposition from machine operators within the estate over correct identification and subsequent management of the plant, culminating in the destruction of a large thicket of laurel. While there remains debate over the associated similarities and differences between the plants, contemporary research indicates the likelihood of a hybridisation between the two species in this niche of woodland, meaning that Japanese laurel may indeed be viewed and treated in a like manner to rhododendron within this habitat niche.

See also

References

  1. ^ "Rhododendron ponticum L." Plants of the World Online. Board of Trustees of the Royal Botanic Gardens, Kew. Retrieved 10 March 2024.
  2. "Infraspecific Taxon Details : Rhododendron ponticum subsp. baeticum (Boiss. & Reuter) Hand.-Mazz". Catalogue of Life. Retrieved 21 November 2020.
  3. ^ "Infraspecific Taxon Details : Rhododendron ponticum subsp. ponticum". Catalogue of Life. Retrieved 21 November 2020.
  4. "Infraspecific Taxon Details : Rhododendron ponticum var. heterophyllum R. Ansin". Catalogue of Life. Retrieved 21 November 2020.
  5. "A adelfeira de Monchique". University of Évora. 13 March 2018. Retrieved 21 November 2020.
  6. ^ Cross, JR (1975). "Rhododendron ponticum L.". Journal of Ecology. 63 (1): 345–364.
  7. Alice M. Coats, Garden Shrubs and Their Histories (1964) 1992, s.v. "Rhododendron"; http://www.countrysideinfo.co.uk/rhododen.htm#Introduction%20to%20Britain .
  8. Hayes, Andrew Wallace (2007). Principles and methods of toxicology. CRC Press. p. 998. ISBN 978-0-8493-3778-9.
  9. Erdemoglu, Nurgun; Akkol, Esra Küpeli; Yesilada, Erdem; Calış, Ihsan (2008-09-02). "Bioassay-guided isolation of anti-inflammatory and antinociceptive principles from a folk remedy, Rhododendron ponticum L. leaves". Journal of Ethnopharmacology. 119 (1): 172–178. doi:10.1016/j.jep.2008.06.021. ISSN 0378-8741. PMID 18638535.
  10. "New flora and fauna for old". The Economist. 2000-12-21. Archived from the original on 2001-07-28. Retrieved 2008-12-14.
  11. "Rhododendron: A killer of the Countryside". Offwell Woodland & Wildlife Trust. 2004. Retrieved 30 May 2010.
  12. "BREAKTHROUGH IN BATTLE AGAINST PROBLEM PONTICUM". Forestry Commission. 30 July 2004. Archived from the original on 5 March 2011. Retrieved 30 May 2010.
  13. Tiedeken, Erin Jo; Egan, Paul A.; Stevenson, Philip C.; Wright, Geraldine A.; Brown, Mark J. F.; Power, Eileen F.; Farrell, Iain; Matthews, Sharon M.; Stout, Jane C.; Manson, Jessamyn (November 2015). "Nectar chemistry modulates the impact of an invasive plant on native pollinators" (PDF). Functional Ecology. 30 (6): 885–893. doi:10.1111/1365-2435.12588.
  14. Scott-Brown, AS, Gregory, T, Farrell, IW, Stevenson PC. (2016). "Leaf trichomes and foliar chemistry mediate defence against glasshouse thrips; Heliothrips haemorrhoidalis (Bouché) in Rhododendron simsii". Functional Plant Biology. 43 (12): 1170–1182. doi:10.1071/FP16045. PMID 32480536.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  15. Milne, R.I. and Abbott, R.J., 2000. Origin and evolution of invasive naturalized material of Rhododendron ponticum L. in the British Isles. Molecular Ecology, 9(5), pp. 541–556.

External links

Taxon identifiers
Rhododendron ponticum
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