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Title: Cassytha  
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Subject: Lauraceae, Rhipsalis, Cassytha filiformis, Cuscuta, Parasitic plants
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Cassytha filiformis
Scientific classification
Kingdom: Plantae
(unranked): Angiosperms
(unranked): Magnoliids
Order: Laurales
Family: Lauraceae
Genus: Cassytha

See text

Cassytha ciliolata, showing flower buds, flowers, fruit, and haustoria both on its own stems and host bark

Cassytha is a genus of some two dozen species of obligately parasitic vines in the family Lauraceae. Superficially, and in some aspects of their ecology, they closely resemble plants in the unrelated genus Cuscuta, the dodders.[1] The physical resemblance is so close, when fruit and flowers are absent in the field, few people without technical training can tell them apart. The two genera present a spectacular example of convergent evolution.[2] In its divergence from habits typical of the Lauraceae, Cassytha also presents examples of mosaic evolution[3]

Several species of Cassytha are regarded as pests in some regions, though in general they are not as serious a problem as the true dodders. Some even yield a welcome harvest of fruit, or are valued for their perceived medicinal or aphrodisiac properties, partly because, like many members of the Lauraceae, some are fragrant when bruised.[4][5] Their stems make useful strings for construction of thatched roofs and certain styles of lei and the like.[6]


  • Common names and confusion 1
  • Context and distribution 2
  • Botanical details 3
  • Reproduction and ecology 4
  • Uses 5
  • References 6
  • Further reading 7

Common names and confusion

Probably the most useful common names for Cassytha species are laurel dodder or dodder laurel, because they look like dodder and are in the laurel family, Lauraceae. The name love vine has merit because some species, in particular C. filiformis, are regarded as aphrodisiacs in the Caribbean region.[7] [8] In practice, however, the confusion between the various species of Cassytha and Cuscuta is so natural, their common names are more or less interchangeable. Practically all the common names for dodder are widely applied in error to Cassytha, as well, but as a matter of convenience in Florida at least, where members of both groups of plants are present as agricultural pests, a publication of the Department of Agriculture adopts the names woe vine for Cassytha and dodder for Cuscuta.[9]

Context and distribution

Though the Lauraceae constitute a large family, with thousands of species in tens of genera, Cassytha is its only known parasitic genus,[10] and its climbing habit also is atypical of the family; most Lauraceae are woody shrubs or trees. The genus at one time was assigned its own family, Cassythaceae, but currently agreement on its inclusion into the Lauraceae is general.[2][11]

For a genus of such a modest size, Cassytha, as currently defined, has a wide distribution. Most known species are native to Australia, but a few species are indigenous to Africa, southern Asia, various islands, and regions in the Americas. Some species seem to have been spread inadvertently by human agency and probably by birds, as well, and they now occur on several continents; C. filiformis, for example, grows in Hawaii (where it is said to be indigenous),[12] the Australasian ecozone, northern South America, Central America, southern Florida, Japan,[13] and South Africa.[14] It also appears to have been transported to many major islands, and now is effectively pantropical.

Botanical details

The genus is cited as Cassytha L., Sp. Pl. 35 (1753), meaning Carl Linnaeus formally described it in 1753 in his monumental work, Species Plantarum. Otto Stapf updated the work in Flora Capensis in 1912.[15]

Cassytha is unusual among Lauraceae in at least two respects: they are scandent herbs, and they are obligate parasites. Their stems are thread-like or wiry, and like most twining species, they twine clockwise round the host as seen from the source of growth.[16] The vines generally turn yellowish once they have established themselves on a productive host.[10] Cassytha species are stem parasites, adhering to their hosts by uniseriate haustoria that generally are small and oblong. Their leaves are without stipules, alternate, simple, and easily overlooked, being minute and scale-like.

Various species of Cassytha bear flowers in racemes, spikes, or heads. Depending on the species, the flowers are sessile or pedicellate. The individual flowers are hermaphroditic and bracteolate, each being attended by a bract and two smaller bracteoles. In general, the flowers are small, so much so that in many species they are inconspicuous.[17]

The perianth has six tepals, the three outer tepals smaller than the inner. The 12 stamens are in four whorls. The receptacle of the fertilised fruit gradually envelops the ovary, becoming the fleshy part of the ripe fruit, it often retains the dried remnants of the perianth at its tip. In effect, the fruit is a tiny drupe. The endocarp is bony and plays an important part in the reproductive process, both in protecting the seed while the fruit is eaten and in inhibiting germination until the endocarp decays, thereby permitting long-lived soil seed banks to accumulate.[18][19]

List of accepted Cassytha species.[20]- Unresolved species marked with *
Species Authority Range
Cassytha aurea J.Z.Weber Australia
Cassytha candida (J.Z.Weber) J.Z.Weber Australia
Cassytha capillaris Meisn. Australia, Malaysia, New Guinea, Thailand
Cassytha ceratopoda * Meisn.
Cassytha ciliolata Nees South Africa
Cassytha coronata * Nees
Cassytha filiformis L. The Americas, Australasia, Indomalaya, East Africa and Polynesia.
Cassytha flava Nees Australia
Cassytha flindersii (J.Z.Weber) J.Z.Weber Australia
Cassytha glabella (Nees) J.Z.Weber Australia, Okinawa
Cassytha larsenii Kosterm.
Cassytha major * Gray
Cassytha melantha R.Br. Australia
Cassytha micrantha Meisn. Australia
Cassytha nodiflora Meisn. Australia
Cassytha paniculata R.Br. New Zealand
Cassytha paradoxae Proctor
Cassytha pedicellosa J.Z.Weber
Cassytha peninsularis J.Z.Weber
Cassytha pomiformis Nees Australia
Cassytha pondoensis Engl. South Africa
Cassytha pubescens R.Br. Australia, New Zealand, Okinawa
Cassytha racemosa Nees eastern Australia
Cassytha rubiginosa * E. Mey.
Cassytha rufa J.Z.Weber

Some species of the cactus genus Rhipsalis once were assigned to Cassytha in an error arising from the resemblance in habitus. An unfortunate consequence has been that the homonym Cassytha Mill. (1768) is often mentioned as a synonym of the genus Rhipsalis, although this perception is incorrect, since the generic name Cassytha had already been applied to a completely different genus in a different plant family.

The morphology and ecology of Cassytha are so atypical of the family Lauraceae, they have been the subject of molecular genetic research to confirm their taxonomic relationships. Though special aspects to their phylogeny are certainly, their assignment to the Lauraceae seems undoubtedly correct.[2]

Reproduction and ecology

Cassytha fruits are ecologically valuable to some fruit-eating birds. The birds either regurgitate the seeds or pass them through their guts. Mammals, for example Australian macropods, also transport the seeds in their guts.[12] The bony endocarp that protects the seed in its passage through animal guts also prevents the seed from immediate germination even if conditions are favourable. Instead, the seeds survive on or in the ground till decay weakens the endocarp sufficiently to permit moisture to enter and germination to begin. This process is not deterministic, so some of the seeds might remain inactive in the soil seed bank for many years before they germinate at unpredictable intervals. Accordingly, once soil is infested with large numbers of seeds, long time may be needed to the eradicate the population entirely. On germination, the seedlings behave as aggressive parasites; they twist about till they find a host, and those that fail to locate hosts soon die, typically in a matter of months.[12]

Seedlings and actively growing shoots are green at first, but once their haustoria are fully established on a suitable host, the plants lose most of their chlorophyll and generally become yellowish or orange, and the Cassytha plant abandons its connections with its root, which soon dies.

Cassytha species are perennials; although they attack practically whatever host plants they encounter, including suitable annuals, they seem to show some preference for woody perennial hosts. Consequently, they often find themselves on seasonally dormant host species. When that happens and their supplies largely dry up, the stems of most species of Cassytha turn green until the host once again becomes productive. This suggests such species are at least marginally photosynthetic, but do not invest resources unnecessarily when photosynthesis is not required.[10] Cassytha species do produce some of their own nutrients while green, so their chlorophyll production is genuine.[9]

Technically, Cassytha could be regarded as hemiparasitic rather than holoparasitic, but their own autotrophic contributions are plainly limited to what it takes to tide over temporary shortages. When all the hosts of a plant die, so does the parasite, so whatever the details of their biology, Cassytha species certainly are unconditionally obligately parasitic. No doubt their lack of a persistent root system dooms any Cassytha plants whose hosts supply insufficient water and mineral nutrients.

The effects of Cassytha on host plants varies. They are not very selective and they parasitise hosts from many plant families, often overwhelming a host so drastically as to kill it. Even when host plants survive, a heavy infestation commonly causes drastic reduction in vigour and reproductive capacity. Accordingly, some species of Cassytha have been examined as potential weed control agents, and others are regarded as agricultural pests in their own right.[21]

Although Cassytha species are vigorous parasites, they are less aggressive, and correspondingly less serious agricultural pests, than Cuscuta species; Cuscuta species generally grow several times faster, produce more seed, and germinate more rapidly.[9]

Among their various ecological effects, Cassytha species act as vectors, though not exclusive vectors, for various plant diseases. They may pass various fungi, Agrobacterium species, viruses, and other pathogens to host plants, or from one host plant to another.[9]


Cassytha is best known for its parasitic habit, and the various species are neither prominent as crop plants, nor as beneficial plants at all. However, species within the genus do have minor uses in rural communities around the world. For example, the fruit of various species is eaten, both by birds and by humans, and C. melantha in particular has been documented as a wild-harvested Australian indigenous food.[22] In the Caribbean region, C. filiformis is one of the plant species known as love vine, because it has a reputation as an aphrodisiac.[7]

Plants in the genus contain low concentrations of several alkaloids that have not yet been shown to be of great value, but do have biochemical properties worthy of investigation.[23][24] Together with the fragrant essential oils in some species,[4] the alkaloids might be relevant to the wide application of Cassytha species in folk medicine and in traditional teas.[25]

Though they are not of commercial interest as fibre crops, suitably prepared vines from some Cassytha species are of value in rural communities as a casual source of cord. They may be used for binding bundles of materials such as thatch, or for stringing decorative festoons.[6]


  1. ^ Weber, J. Z. A TAXONOMIC REVISION OF CASSYTHA (LAURACEAE) IN AUSTRALIA. J. Adelaide Bot. Gard. 3(3): 187-262(1981) PDF @
  2. ^ a b c Nickrent, D. L. 2002. Phylogenetic Origins of Parasitic Plants. Chapter 3, pp. 29-56 In J. A. López-Sáez, P. Catalán and L. Sáez [eds.], Parasitic Plants of the Iberian Peninsula and Balearic Islands. Mundi-Prensa, Madrid.
  3. ^ Kuijt, J. 1969. The Biology of Parasitic Flowering Plants. University of California Press, Berkeley, CA.
  4. ^ a b Brophy, Paul I.; Goldsack, Joseph J.; Forster, Robert J. (2009). "The Essential Oils of Some Australian Cassytha Species (Lauraceae)". Journal of Essential Oil Research 21 (6): 543–546.  
  5. ^
  6. ^ a b
  7. ^ a b Esbaugh, W. Hardy; McClure, Susan A. & Bolyard, Judith L. Bush Medicine Studies, Andros Island, Bahamas. Proceedings of the first symposium on the botany of the Bahamas 11–14 June 1985. Ed. Robert R. Smith., San Salvador, Bahamas.
  8. ^
  9. ^ a b c d Haynes, Alan R., Coile, Nancy C., Schubert. Timothy S.; "Comparison of Two Parasitic Vines: Dodder (Cuscuta) and Woe Vine (Cassytha)". Botany Circular No. 30. Fla. Dept Agric. & Consumer Services January/February 1996. Division of Plant Industry
  10. ^ a b c Visser, Johann (1981). South African parasitic flowering plants. Cape Town: Juta.  
  11. ^ Rohwer, J. G. (2000). "Toward a phylogenetic classification of the Lauraceae: Evidence from matK sequences". Syst. Bot. 25: 60–71.  
  12. ^ a b c Nelson, Scot C. "Cassytha filiformis". Plant Disease July 2008 PD-42 Department of Plant and Environmental Protection Sciences. Cooperative extension service. University of Hawaii at Manoa.
  13. ^ Weber, J. Z.:A taxonomic revision of Cassytha (Lauraceae) in Australia. Journal of Adelaide Botanic Gardens 3:187-262, 1981
  14. ^ Arnold T.H., de Wet B.C. (Eds), Plants of Southern Africa: Names & Distribution, MEMOIRS OF THE BOTANICAL SURVEY OF SOUTH AFRICA No. 62, Pub.National Botanical Institute, South Africa.1993 ISBN 1-874907-03-X
  15. ^ Stapf, Otto. Flora Capensis, 5, 1: 500 (1912)
  16. ^ Isnard Sandrine & Silk Wendy K. "Moving with climbing plants from Charles Darwin’s time into the 21st century" doi:10.3732/ajb.0900045 Am. J. Bot. July 2009 vol. 96 no. 7 1205-1221
  17. ^ Coleman, H.R. and Watson, Leslie. Cassytha. October 2008. Western Australian Herbarium (1998–). FloraBase—the Western Australian Flora. Department of Environment and Conservation.
  18. ^ Morris, D.I. (2009) 5 Lauraceae, version 2009:1. In MF Duretto (Ed.) Flora of Tasmania Online. 5 pp. (Tasmanian Herbarium, Tasmanian Museum & Art Gallery: Hobart). ISBN 978-1-921599-03-3 (PDF).
  19. ^ Dyer, R. Allen, "The Genera of Southern African Flowering Plants". ISBN 0-621-02854-1, 1975
  20. ^ The Plant List (2012). Version 1. Published on the Internet; (accessed 22 November 2012)
  21. ^ Tsang, Hong Tai (Steven) (2010), Cassytha pubescens: germination biology and interactions with native and introduced hosts, retrieved 6 January 2012 
  22. ^ Brand Miller, J., James, K.W. and Maggiore, P. (1993) Tables of Composition of Australian Aboriginal Foods. Canberra: Aboriginal Studies Press.
  23. ^ Hoet, S; Stévigny, C; Block, S; Opperdoes, F; Colson, P; Baldeyrou, B; Lansiaux, A; Bailly, C; Quetin-Leclercq, J (May 2004). "Alkaloids from Cassytha filiformis and related aporphines: antitrypanosomal activity, cytotoxicity, and interaction with DNA and topoisomerases". Planta Med. 70 (5): 407–13.  
  24. ^ Stévigny C, Block S, De Pauw-Gillet MC, de Hoffmann E, Llabrès G, Adjakidjé V, Quetin-Leclercq J. Cytotoxic aporphine alkaloids from Cassytha filiformis. Planta Med. 2002 Nov ;68(11):1042-4.
  25. ^ Watt, John Mitchell; Breyer-Brandwijk, Maria Gerdina: The Medicinal and Poisonous Plants of Southern and Eastern Africa 2nd ed Pub. E & S Livingstone 1962

Further reading

  • Cava, M. P.; Rao, Kota V.; Douglas, B.; Weisbach, J. A. (1968). "Alkaloids of Cassytha americana". The Journal of Organic Chemistry 33 (6): 2443–2446.  
  • Chang, Fang-Rong; Chao, Ya-Chieh; Teng, Che-Ming; Wu, Yang-Chang (1998). "Chemical Constituents fromCassythafiliformisII". Journal of Natural Products 61 (7): 863–866.  
  • Johns, SR; Lamberton, JA; Sioumis, AA (1966). "Cassythaalkaloids. II. Alkaloids ofCassytha pubescensR. Br". Australian Journal of Chemistry 19 (12): 2331.  
  • Jones, SR; Lamberton, JA (1966). "Cassythaalkaloids. I. New aporphine alkaloids fromCassytha filiformisL". Australian Journal of Chemistry 19 (2): 297.  
  • Wu, Yang‐Chang; Chang, Fang‐Rong; Chao, Ya‐Chieh; Teng, Che‐Ming (1998). "Antiplatelet and vasorelaxing actions of aporphinoids from Cassytha filiformis". Phytotherapy Research 12 (S1): S39–S41.  
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