Liana
A liana is a long-stemmed, woody vine that is rooted in the soil at ground level and uses trees, as well as other means of vertical support, to climb up to the canopy in search of direct sunlight.[1] The word liana does not refer to a taxonomic grouping, but rather a habit of plant growth – much like tree or shrub. It comes from standard French liane, itself from an Antilles French dialect word meaning to sheave.
Ecology
Lianas are characteristic of tropical moist broadleaf forests (especially seasonal forests), but may be found in temperate rainforests and temperate deciduous forests. There are also temperate lianas, for example the members of the Clematis or Vitis (wild grape) genera. Lianas can form bridges amidst the forest canopy, providing arboreal animals with paths across the forest. These bridges can protect weaker trees from strong winds. Lianas compete with forest trees for sunlight, water and nutrients from the soil.[2] Forests without lianas grow 150% more fruit; trees with lianas have twice the probability of dying.[3]
Lianas may be found in many different plant families. One way of distinguishing lianas from trees and shrubs is based on the stiffness, specifically, the Young's modulus of various parts of the stem. Trees and shrubs have young twigs and smaller branches which are quite flexible and older growth such as trunks and large branches which are stiffer. A liana often has stiff young growths and older, more flexible growth at the base of the stem.[4]
Habitat
Lianas compete intensely with trees, greatly reducing tree growth[5] and tree reproduction,[6] greatly increasing tree mortality,[7] preventing tree seedlings from establishing,[5] altering the course of regeneration in forests,[8] and ultimately affecting tree population growth rates.[9] Lianas also provide access routes in the forest canopy for many arboreal animals, including ants and many other invertebrates, lizards, rodents, sloths, monkeys, and lemurs. For example, in the Eastern tropical forests of Madagascar, many lemurs achieve higher mobility from the web of lianas draped amongst the vertical tree species. Many lemurs prefer trees with lianas for their roost sites.[10] Lianas also provide support for trees when strong winds blow.[11] However, they may be destructive in that when one tree falls, the connections made by the lianas may cause many other trees to fall.[11]
As noted by Charles Darwin, because lianas are supported by other plants, they may conserve resources that other plants must allocate to the development of structure and use them instead for growth and reproduction. In general, lianas are detrimental to the trees that support them. Growth rates are lower for trees with lianas; they directly damage hosts by mechanical abrasion and strangulation, render hosts more susceptible to ice and wind damage, and increase the probability that the host tree falls. Lianas also make the canopy of trees more accessible to animals which eat leaves. Because of these negative effects, trees which remain free of lianas are at an advantage; some species have evolved characteristics which help them avoid or shed lianas.[12]
Examples
Some families and genera containing liana species include:
- Gnetophyta
- Gnetum
- Acanthaceae
- Mendoncia
- Thunbergia, such as T. grandiflora and T. mysorensis
- Anacardiaceae
- Attilaea
- Rhus
- Toxicodendron
- Ancistrocladaceae
- Ancistrocladus
- Annonaceae
- Artabotrys
- Fissistigma
- Uvaria
- Apocynaceae
- Odontadenia
- Stephanotis
- Strophanthus, e.g S. sarmentosus
- Arecaceae
- Calamus
- Daemonorops
- Araceae
- Pothos, e.g. P. lancifolius
- Aristolochiaceae
- Aristolochia
- Bignoniaceae
- Anemopaegma
- Pyrostegia
- Capparaceae
- Capparis
- Celastraceae
- Celastrus
- Connaraceae
- Connarus
- Dilleniaceae
- Doliocarpus[2]
- Dioscoreaceae
- Dioscorea, e.g. D. sylvatica
- Fabaceae
- some Acacia, e.g. A. concinna
- Callerya megasperma
- Dalbergia armata
- Derris
- Entada
- Hultholia mimosoides
- Machaerium
- Mezoneuron
- Mucuna, e.g. M. bennettii
- Pterolobium
- Lasiobema
- Strongylodon, e.g. S. macrobotrys
- Wisteria
- Flagellariaceae
- Flagellaria indica
- Loganiaceae
- Strychnos, e.g. S. axillaris
- Nepenthaceae
- Nepenthes
- Nyctaginaceae
- Oleaceae
- Polygalaceae
- Moutabea, e.g. M. Aculeata
- Rosaceae
- Rosa banksiae
- Sapindaceae
- Paullinia
- Rhamnaceae
- Ventilago
- Ziziphus
- Rubiaceae
- Uncaria
- Rutaceae
- Toddalia asiatica
- Schlegeliaceae
- Schlegelia
- Smilacaceae
- Smilax
- Verbenaceae
- Petrea, e.g. P. volubilis
- Vitaceae
- Ampelopsis
- Cissus, e.g. C. hypoglauca
- Parthenocissus
- Tetrastigma
- Vitis
References
- "liana". Encyclopædia Britannica.
- Schnitzer, S. A.; Bongers, F. (2002). "The ecology of lianas and their role in forests". Trends in Ecology and Evolution. 17 (5): 223–230. doi:10.1016/S0169-5347(02)02491-6.
- Landers, Jackson (13 June 2017). "Tarzan's Favorite Mode of Travel, the Liana Vine, Chokes Off a Tree's Ability to Bear Fruit". Smithsonian. Retrieved 20 June 2017.
- Lahaye, R.; Civeyrel, L.; Speck, T.; Rowe, N. P. (2005). "Evolution of shrub-like growth forms in the lianoid subfamily Secamonoideae (Apocynaceae s.l.) of Madagascar: phylogeny, biomechanics, and development". American Journal of Botany. 92 (8): 1381–96. doi:10.3732/ajb.92.8.1381. PMID 21646158.
- Schnitzer, S. A.; Carson (2010). "Lianas suppress tree regeneration and diversity in treefall gaps". Ecology Letters. 13 (7): 849–857. doi:10.1111/j.1461-0248.2010.01480.x. PMID 20482581.
- Wright, S. J.; Jaramillo, A. M.; Pavon, J.; Condit, R.; Hubbell, S. P.; Foster, R. B. (2005). "Reproductive size thresholds in tropical trees: variation among individuals, species and forests". Journal of Tropical Ecology. 21 (3): 307–315. doi:10.1017/S0266467405002294. S2CID 42171771.
- Ingwell, L. L.; Wright, S. J.; Becklund, K. K.; Hubbell, S. P.; Schnitzer, S. A. (2010). "The impact of lianas on 10 years of tree growth and mortality on Barro Colorado Island, Panama". Journal of Ecology. 98 (4): 879–887. doi:10.1111/j.1365-2745.2010.01676.x.
- Schnitzer, S. A.; Dalling, J. W.; Carson, W. P. (2000). "The impact of lianas on tree regeneration in tropical forest canopy gaps: Evidence for an alternative pathway of gap-phase regeneration". Journal of Ecology. 88 (4): 655–666. doi:10.1046/j.1365-2745.2000.00489.x.
- Visser, Marco D.; Schnitzer, Stefan A.; Muller-Landau, Helene C.; Jongejans, Eelke; de Kroon, Hans; Comita, Liza S.; Hubbell, Stephen P.; Wright, S. Joseph; Zuidema, Pieter (2018). "Tree species vary widely in their tolerance for liana infestation: A case study of differential host response to generalist parasites". Journal of Ecology. 106 (2): 781–794. doi:10.1111/1365-2745.12815. ISSN 0022-0477.
- Rendigs, A.; Radespiel, U.; Wrogemann, D.; Zimmermann, E. (2003). "Relationship between microhabitat structure and distribution of mouse lemurs (Microcebus spp.) in northwestern Madagascar". International Journal of Primatology. 24 (1): 47–64. doi:10.1023/A:1021494428294. S2CID 20661112.
- Garrido-Pérez, E. I.; Dupuy, J. M.; Durán-García, R.; Gerold, G.; Schnitzer, S. A.; Ucan-May, M. (2008). "Structural effects of lianas and hurricane Wilma on trees in Yucatan peninsula, Mexico". Journal of Tropical Ecology. 24 (5): 559–562. doi:10.1017/S0266467408005221.
- Putz, F. E. (1984). "How trees avoid and shed lianas". Biotropica. 16 (1): 19–23. doi:10.2307/2387889. JSTOR 2387889.
External links
- Lianas and Climbing Plants of the Neotropics
- Lianas and Climbing Plants of the Neotropics: Family Treatments
- 'Vines and Lianas' by Rhett Butler, at http://rainforests.mongabay.com/0406.htm
- . . 1914.