Langbahn Team – Weltmeisterschaft

Persea

Persea
Temporal range: Eocene–Present[1]
Persea indica foliage and fruit
Avocado (Persea americana) foliage
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Magnoliids
Order: Laurales
Family: Lauraceae
Genus: Persea
Mill.[2]
Type species
Persea americana
Species

See text. Complete list

Synonyms

Persea is a genus of about 150 species of evergreen trees belonging to the laurel family, Lauraceae.[3] The best-known member of the genus is the avocado, P. americana, widely cultivated in subtropical regions for its large, edible fruit.

Overview

They are medium-size trees, 15–30 m (49.2–98.4 ft) tall at maturity. The leaves are simple, lanceolate to broad lanceolate, varying with species from 5–30 cm (1.97–11.81 in) long and 2–12 cm (0.79–4.72 in) broad, and arranged spirally or alternately on the stems. The flowers are in short panicles, with six small greenish-yellow perianth segments 3–6 mm (0.12–0.24 in) long, nine stamens and an ovary with a single embryo. The fruit is an oval or pear-shaped berry,[4] with a fleshy outer covering surrounding the single seed; size is very variable among the species, from 1–1.5 cm (0.39–0.59 inches) in e.g. P. borbonia and P. indica, up to 10–20 cm (3.94–7.87 inches) in some cultivars of P. americana.

Distribution and ecology

Persea americana flowers

The species of Persea have a disjunct distribution, with about 70 Neotropical species, ranging from Brazil and Chile in South America to Central America and Mexico, the Caribbean, and the southeastern United States; a single species, P. indica, endemic to Madeira and the Canary Islands off northwest Africa; and 80 species inhabiting east and southeast Asia. None of the species are very tolerant of severe winter cold, with the hardiest, P. borbonia, P. ichangensis and P. lingue, surviving temperatures down to about −12 °C (10.4 °F); they also require continuously moist soil, and do not tolerate drought. A number of these species are found in forests that face threats of destruction or deforestation; for example, P. lingue in Central Chile.

The family Lauraceae was part of the land flora of Gondwana, and many genera had migrated to South America via Antarctica over ocean landbridges by the time of the Paleocene. From South America they spread over most of the continent. When the North American and South American tectonic plates joined in the late Neogene, volcanic mountain building created island chains which later formed the Mesoamerican landbridge. Pliocene elevation created new habitats for speciation. While some genera died out in increasingly xerophytic mainland Africa, starting with the freezing of Antarctica about 20 million years ago and the formation of the Benguela current, others, which also reached South America and Mesoamerica, such as Beilschmiedia and Nectandra are still surviving today in Africa in a number of species. The genus, however, died out in Africa, except for P. indica, which is, today, a threatened species that survives in the fog-shrouded mountains of the Canary Islands and Madeira.

Fossil evidence indicates that the genus originated in West Africa during the Paleocene, and spread to Asia, to South America, and to Europe and thence to North America. It is thought that the gradual drying of Africa, west Asia, and the Mediterranean from the Oligocene to the Pleistocene, and the glaciation of Europe during the Pleistocene, caused the extinction of the genus across these regions, resulting in the present distribution.

Since this habitat is constantly threatened by encroaching agriculture, the laurel forest animal or vegetal species have already become rare in many of its former habitats and are threatened by further habitat loss.

In Mesoamerica, Persea proliferated into many new species, and the berries of some of them constitute a valuable food supply for quetzals, trogoniform birds that live in the montane rainforests of Mesoamerica. In particular, the resplendent quetzal's favorite fruits are berries of wild relatives of the avocado. Their differing maturing times in the cloudforest determine the migratory movements of the quetzals to differing elevation levels in the forests. With a gape width of 21 mm (0.83 in), the quetzal swallows the small berry (aguacatillo) whole, which he catches while flying through the lower canopy of the tree, and then regurgitates the seed within 100 meters (328 ft) from the tree. Wheelright in 1983 observed that parent quetzals take far less time intervals to deliver fruits to the young brood than insects or lizards, reflecting the ease of procuring fruits, as opposed to capturing animal prey. Since the young are fed exclusively berries in the first 2 weeks after hatching, these berries must be of high nutritional value. Usually only the total percentage of water, sugar, nitrogen, crude fats and carbohydrates are reported by ornithologists.[5]

Persea species are also used as food plants by the larvae of some Lepidoptera species including giant leopard moth, Coleophora octagonella (which feeds exclusively on P. carolinensis) and Hypercompe indecisa.

Classification

The genus Persea is treated in three subgenera. The Asian subgenus Machilus is treated in a separate genus Machilus by many authors, including in the Flora of China, while graft-incompatibility between subgenus Persea and subgenus Eriodaphne suggests that these too may be better treated as distinct genera, in fact Kostermans (1993) founded the genus Mutisiopersea for these. Another closely related genus, Beilschmiedia, is also sometimes included in Persea.

In a phylogenetic analysis of the "Persea group", which also includes Alseodaphne, Phoebe, Nothaphoebe, Dehaasia and Apollonias, Persea was found to be mostly monophyletic, with Apollonias barbujana from the Canary Islands nested within the core Persea group. The species Persea nudigemma was found to be more closely related to Phoebe, while Persea sphaerocarpa was found to be nested within a group of Alseodaphne species.[6]

The avocado fruit, Persea americana
Subgenus PerseaCentral America. Two species.
  • Persea americana Mill. – Avocado
    • Persea americana var. drymifolia (Schltdl. & Cham.) S.F.Blake
    • Persea americana var. floccosa (Mez) Scora
    • Persea americana var. guatemalensis (L.O.Williams) Scora
    • Persea americana var. nubigena (L.O.Williams) L.E.Kopp
    • Persea americana var. steyermarkii (C.K.Allen) Scora
  • Persea schiedeana Nees – Coyo
Persea borbonia
Subgenus Eriodaphne (Mutisiopersea) — The Americas, Macaronesia. About 70 species, including
Persea macrantha leaves
Subgenus MachilusAsia. About 80 species, including

Formerly placed here

Phylogeny

Based on[6]

clade I  

Mac. robusta

Mac. sp. W14071

Mac. sp. W14068

Pho. minutiflora

Mac. japonica

Mac. decursinervis

Mac. grijsii

Mac. platycarpa

Mac. yunnanensis

Mac. kwangtungensis

Mac. oculodracontis

Mac. duthiei

Mac. gamblei

Mac. oreophila

Mac. leptophylla

Pho. faberi

Mac. salicoides

Mac. pomifera

Mac. salicina

Mac. thunbergii

Mac. breviflora

Mac. pingii

Mac. shweliensis

Mac gongshanensis

Mac. phoenicis

Mac. monticola

Deh. caesia

Deh. hainanensis

Als. sp. W17084

Deh. sp. L20070187

Als. semecarpifolia

Als. huanglianshanensis

Als. gigaphylla

Not. umbelliflora

Deh. sp. A34

Deh. incrassata

clade II  
Persea clade I   

Per. aurata

Per. splendens

Per. major

Per. weberbaueri  

Per. sp. V25232

Per. sp. W19517

Per. alba

Per. sp. W14875

Per. sp. B21834

Per. lingue

Per. caerulea

Per. borbonia

Per. haenkeana

Per. palustris

Per. indica

Per. areolatocostae

Persea clade II   

Per. americana

Per. styermarkii

Apo. barbujana

clade III  
Phoebe clade I  

Pho. formosana

Pho. chekiangensis  

Pho. nanmu

Pho. neurantha

Pho. lanceolata

Pho. sp. L20070260

Pho. zhennan

Pho. macrocarpa

Pho. angustifolia

Phoebe clade II  

Pho. cuneata

Pho. elliptica

Pho. sp. A49

Pho. puwenensis

Pho. hungmaoensis

Pho. megacalyx

Per. nudigemma

Als. rugosa

Als. hainanensis  

Als. sp. W14264

Per. sphaerocarpa

Per. sp. W21874

Als. petiolaris

Als. andersonii

Neo. sericea

Neo. howii

Neo. cambodiana  

Act. cupularis

Act. trichocarpa

Lit. verticillata

Lin. megaphylla

Lit. auriculata

Lin. erythrocarpa

Machias clade
Alseodaphne-Dehaasia clade
Persea clade
Phoebe clade
Alseodaphne-Persea group
Outgroups

Etymology

Philip Miller derived Persea from the Greek name Περσέα. It was applied by Theophrastus and Hippocrates to an uncertain Egyptian tree, possibly Cordia myxa or a Mimusops species.[8]

References

  1. ^ Vento, B.; Prámparo, Mercedes B. (2018). "Angiosperm association from the Río Turbio Formation (Eocene–?Oligocene) Santa Cruz, Argentina: revision of Hünicken's (1955) fossil leaves collection". Alcheringa: An Australasian Journal of Palaeontology. 42 (1): 125–153. Bibcode:2018Alch...42..125V. doi:10.1080/03115518.2017.1408854. hdl:11336/87290. ISSN 0311-5518.
  2. ^ a b "Genus: Persea Mill". Germplasm Resources Information Network. United States Department of Agriculture. 2007-10-05. Retrieved 2011-02-05.
  3. ^ André Joseph Guillaume Henri Kostermans. 1993
  4. ^ Frederick B. Essig (3 March 2015). Plant Life: A Brief History. Oxford University Press. pp. 162–. ISBN 978-0-19-026658-5.
  5. ^ Peter Scora; Rainer W. Scora (1999). "Phytochemistry of Nectandra umbrosa Berries, Cloudforest Food of the Resplendent Quetzal" (PDF). Yearbook. Vol. 83. Moreno Valley, CA: California Avocado Society. pp. 163–171.
  6. ^ a b Li, Lang; Li, Jie; Rohwer, Jens G.; van der Werff, Henk; Wang, Zhi-Hua; Li, Hsi-Wen (September 2011). "Molecular phylogenetic analysis of the Persea group (Lauraceae) and its biogeographic implications on the evolution of tropical and subtropical Amphi-Pacific disjunctions". American Journal of Botany. 98 (9): 1520–1536. doi:10.3732/ajb.1100006. PMID 21860056.
  7. ^ a b "GRIN Species Records of Persea". Germplasm Resources Information Network. United States Department of Agriculture. Archived from the original on 2000-10-27. Retrieved 2011-02-05.
  8. ^ Quattrocchi, Umberto (2000). CRC World Dictionary of Plant Names. Vol. 3 M-Q. CRC Press. p. 2015. ISBN 978-0-8493-2677-6.

Bibliography