Derivation of specific name
Central and East Mexico
State - Kerala, District/s: Idukki"
Sierra Madre Oriental Pine-oak Forests Habitat
This taxon is found in the Sierra Madre Oriental pine-oak forests, which exhibit a very diverse community of endemic and specialized species of plants, mammals, reptiles and amphibians. These high mountains run north to south, beginning in the USA and ending in Mexico. The Sierra Madre Oriental pine-oak forests are a highly disjunctive ecoregion, owing to the fact that they are present only at higher elevations, within a region with considerable expanses of lower elevation desert floor.
The climate is temperate humid on the northeastern slope, and temperate sub-humid on the western slope and highest portions of the mountain range. Pine-oak forest habitat covers most of the region, even though most of the primary forest has been destroyed or degraded. However, the wettest portions house a community of cloud forests that constitute the northernmost patches of this vegetation in Mexico. The forests grow on soils derived from volcanic rocks that have a high content of organic matter. The soils of lower elevations are derived from sedimentary rocks, and some of them are formed purely of limestone. In the northernmost portions of the ecoregion, the forests occur on irregular hummocks that constitute biological "islands" of temperate forest in the middle of the Chihuahuan Desert. To the south, from Nuevo León southward until Guanajuato and Queretaro, the ecoregion is more continuous along the mainstem of the Sierra Madre Oriental.
Dominant tree species include the pines: the endemic Nelson's Pine (Pinus nelsonii), Mexican Pinyon (P. cembroides), Smooth-bark Mexican Pine (P. pseudostrobus), and Arizona Pine (P. arizonica); and the oaks Quercus castanea and Q. affinis. In mesic environments, the most common species are P. cembroides, and Alligator Juniper (Juniperus deppeana), but in more xeric environments on the west slopes of the mountains, the endemic P. pinceana is more abundant. Gregg's Pine (P. greggii) and Jelecote Pine (P. patula) are endemic.
Many mammalian species wander these rugged hills. Mule Deer (Odocoileus hemionus), Puma (Puma concolor), Cliff Chipmunk (Tamias dorsalis), Collared Peccary (Tayassu tajacu), Coati (Nasua narica), Jaguar (Panthera onca) and Coyote (Canis latrans) are a few of the many diverse mammals that inhabit this ecoregion. Some threatened mammals found in the ecoregion are: Bolaños Woodrat (Neotoma palatina VU); Diminutive Woodrat (Nelsonia neotomodon NT), known chiefly from the western versant of the Sierra Madre; Chihuahuan Mouse (Peromyscus polius NT); and Mexican Long-nosed Bat (Leptonycteris nivalis EN).
A considerable number of reptilian taxa are found in the Sierra Madre Oriental pine-oak forests, including three endemic snakes: Ridgenose Rattlesnake (Crotalus willardi); Fox´s Mountain Meadow Snake (Adelophis foxi); and the Longtail Rattlesnake (Crotalus stejnegeri VU), restricted to the central Sierra Madre. An endemic skink occurring in the ecoregion is the Fair-headed Skink (Plestiodon callicephalus). The Striped Plateau Lizard (Sceloporus virgatus) is endemic to the ecoregion. The Sonoran Mud Turtle (Kinosternon sonoriense VU) is found in the ecoregion and ranges from southwestern New Mexico south to northwestern Chihuahua.
The following anuran taxa occur in the Sierra Madre Oriental pine-oak forests: Red-spotted Toad (Anaxyrus punctatus); Cane Toad (Rhinella marina); Elegant Narrow-mouthed Toad (Gastrophryne elegans); New Mexico Spadefoot Toad (Spea multiplicata); Sinaloa Toad (Incilius mazatlanensis); Pine Toad (Incilius occidentalis); Southwestern Toad (Anaxyrus microscaphus); Woodhouse's Toad (Anaxyrus woodhousii); Great Plains Narrowmouth Toad (Gastrophryne olivacea); Great Plains Toad (Anaxyrus cognatus); Plateau Toad (Anaxyrus compactilis); Texas Toad (Anaxyrus speciosus); Sonoran Desert Toad (Incilius alvarius), found only at lower ecoregion elevations here; Rana-ladrona Silbadora (Eleutherodactylus teretistes); Sabinal Frog (Leptodactylus melanonotus); Mexican Leaf Frog (Pachymedusa dacnicolor); Montezuma Leopard Frog (Lithobates montezumae); Yavapai Leopard Frog (Lithobates yavapaiensis); Northwest Mexico Leopard Frog (Lithobates magnaocularis); Bigfoot Leopard Frog (Lithobates megapoda), who generally breeds in permanent surface water bodies; Mexican Cascade Frog (Lithobates pustulosus); Tarahumara Frog (Lithobates tarahumarae VU); Western Barking Frog (Craugastor augusti); Lowland Burrowing Frog (Smilisca fodiens); Taylor's Barking Frog (Craugastor occidentalis); Blunt-toed Chirping Frog (Eleutherodactylus modestus VU), found only at the very lowest elevations of the ecoregion; Shiny Peeping Frog (Eleutherodactylus nitidus); California Chorus Frog (Pseudacris cadaverina); Rio Grande Frog (Lithobates berlandieri); Madrean Treefrog (Hyla eximia); Mexican Treefrog (Smilisca baudinii); Dwarf Mexican Treefrog (Tlalocohyla smithii); Canyon Treefrog (Hyla arenicolor); Northern Sheep Frog (Hypopachus variolosus); Chiricahua Leopard Frog (Lithobates chiricahuensis). There are three salamanders found in the ecoregion: the endemic Sacramento Mountains Salamander (Aneides hardii), found only in very high montane reaches above 2400 meters; Tiger Salamander (Ambystoma tigrinum); and the Tarahumara Salamander (Ambystoma rosaceum).
Belizean Pine Forests Habitat
This species is found in the Belizean pine forests along the Central America's northwestern Caribbean Sea coast; the ecoregion exhibits relatively well preserved fragments of vegetation as well as a considerable abundance of fauna. This ecoregion comprises a geographically small portion of the total land area of the ecoregions of Belize. There is relatively low endemism in the Belizean pine forests, and only a moderate species richness here; for example, only 447 vertebrate taxa have been recorded in the ecoregion. The ecoregion represents one of the few examples of lowland and premontane pine forests in the Neotropics, where the dominant tree species is Honduran Pine (Pinus caribaea var. hondurensis), which requires periodic low intensity burns for its regeneration. The vegetation is adapted to the xeric, acidic and nutrient-poor conditions that occur primarily in the dry season.
In the forest of the Maya Mountains, vegetation reaches higher altitudes, the topography is more rugged and crossed by various rivers, and nighttime temperatures are lower. The pine trees are larger and numerous, and the pine forest intersects other formations of interest such as rainforest, Cohune Palm (corozal), cactus associations, and others. About eleven percent of Belize is covered by natural pine vegetation. Only two percent represents totally closed forests; three percent semi-closed forests; and the remaining six percent pine savannas, that occupy coastal areas and contain isolated pine trees or stands of pine trees separated by extensive pastures. In addition to human activity, edaphic factors are a determining matter in this distribution, since the forests on the northern plain and southern coastal zone are on sandy soils or sandy-clay soils and usually have less drainage than the more fertile soils in the center of the country.
At elevations of 650 to 700 metres, the forests transition to premontane in terms of vegetation. At these higher levels, representative tree species are Egg-cone Pine (Pinus oocarpa), which crosses with Honduras Pine (P. hondurensis), where distributions overlap, although belonging to subsections of different genera; British Honduras Yellowwood (Podocarpus guatemalensis) and Quercus spp.; moreover, and in even more moist areas there is a predominance of Jelecote Pine (Pinus patula), together with the palm Euterpe precatoria var. longivaginata and the arboreal ferns Cyathea myosuroides and Hemitelia multiflora.
A number of reptilian species are found in the Belizean pine forests, including: Guatemala Neckband Snake (Scaphiodontophis annulatus); Indigo Snake (Drymarchon corais); On the coasts, interior lakes and rivers of Belize and by extension in this ecoregion there are two species of threatened crocodiles: American Crocodile (Crocodylus acutus) and Morelet's Crocodile (C. moreletii), while observation of the Central American River Turtle (Dermatemys mawii CR) is not uncommon in this ecoregion.
Also to be noted is the use of this habitat by the Mexican Black Howler (Alouatta pigra), which can be considered the most endangered howler monkey of the genus, and the Central American spider monkey (Atteles geoffroyi). Both species experienced a decline due to the epidemic yellow fever that swept the country in the 1950s. The five feline species that exist in Belize: Jaguar (Panthera onca), Puma (F. concolor), Ocelot (Leopardus pardalis), Margay (Leopardus wiedii) and Jaguarundí (Herpailurus yagouaroundi) are in appendix I of CITES, as well as the Central American tapir (Tapirus bairdii) can been seen with relative frequency. Belize has the highest density of felines in Central America. The tapir is abundant around rivers. The White-lipped Peccary (Tayassu pecari) is also present in the ecoregion.
Although most of the amphibians and reptiles are found in humid premontane and lowland forests, the only endemic frog in this ecoregion, Maya Mountains Frog (Lithobates juliani), is restricted to the Mountain Pine Ridge in the Maya Mountains. Salamanders in the ecoregion are represented by the Alta Verapaz Salamander (Bolitoglossa dofleini NT), whose males are arboreal, while females live under logs. Anuran taxa found in the ecoregion include: Rio Grande Frog (Lithobates berlandieri); Sabinal Frog (Leptodactylus melanonotus); Northern Sheep Frog (Hypopachus variolosus); Stauffer's Long-nosed Treefrog (Scinax staufferi); and Tungara Treefrog (Engystomops pustulosus).
Present in the ecoregion are a number of avian species, including the endangered Yellow-headed Amazon Parrot (Amazona oratrix EN), although this bird is adversely affected by ongoing habitat destruction. Of particular interest is the presence in this ecoregion of Central America's highest procreative colony of Jabiru (Jabiru mycteria), a large migratory bird, particularly in the Crooked Tree sanctuary, on the country's northern plains.
Habitat and Ecology
erumpent pycnidium of Phomopsis coelomycetous anamorph of Diaporthe eres is saprobic on twig of Pinus patula
In Great Britain and/or Ireland:
Foodplant / mycorrhiza / ectomycorrhiza
fruitbody of Suillus luteus is ectomycorrhizal with live root of Pinus patula
Remarks: captive: in captivity, culture, or experimentally induced
Foodplant / mycorrhiza / ectomycorrhiza
fruitbody of Thelephora terrestris is ectomycorrhizal with live root of Pinus patula
Remarks: captive: in captivity, culture, or experimentally induced
Life History and Behavior
Molecular Biology and Genetics
Barcode data: Pinus patula
Statistics of barcoding coverage: Pinus patula
Public Records: 4
Specimens with Barcodes: 9
Species With Barcodes: 1
IUCN Red List Assessment
Red List Category
Red List Criteria
Pinus patula is widespread and abundant despite exploitation for its timber. Regeneration is quick and the trees are fast growing. It is therefore assessed as Least Concern.
- 1998Lower Risk/least concern (LR/lc)
|This article includes a list of references, but its sources remain unclear because it has insufficient inline citations. (June 2013)|
Patula pine, pino patula, pinus patula (spreading-leaved pine, Mexican weeping pine, pino llorón in Spanish)(patula Latin = spreading) is a tree native to the highlands of Mexico. It grows from 24° to 18° North latitude and 1800 to 2700 m above sea level. 30 m tall. It does not stand long periods of temperatures as low as –10°C, but resists occasional brief below zero dips. It is moderately drought-tolerant, in this scope is superior than Pinus taeda. Rainfall range is from 750 to 2000 mm annual average, it happens mostly in summer but in a little area of the State of Veracruz on the Sierra Madre Oriental its habitat is rainy year round.
It is planted at high altitudes in Ecuador (3500 m), Bolivia, Colombia (3300m), Kenya, Tanzania, Angola, Zimbabwe, Papua New Guinea, and Hawaii (3000 m). In Hawaii it is replacing the native alpine grassland.
At lower altitudes than its origin country it is cultivated in Southern Brazil, South Africa, India, and in the Argentine provinces of Córdoba and San Luis. it is planted for forestation purposes in lands originally covered by bushland.
It has been introduced near sea level in New South Wales, Australia, where it spreads naturally by wind and is very favored because rainfalls are more abundant in summer. It was also introduced in New Zealand for commercial purposes and is fully naturalized there. It is cultivated in the United Kingdom as an ornamental tree for parks and gardens, and has gained the Royal Horticultural Society's Award of Garden Merit.
The timber is pale-pink to salmon, moderately soft, brittle and smelling strongly of aniseed when freshly cut.
There are two varieties:
1. P. patula Schiede ex Schlechtendal et Chamisso var. patula. Type Mexico, Veracruz: Cruz Blanca, "Inter Cruz blanca & Jalacingo," 1828.11, Schiede and Deppe 1108 (lectotype, HAL). Syn.: Pinus patula Schiede ex Schlechtendal et Chamisso var. macrocarpa M.T. Masters, Gard. Chron., ser. 3, 9: 438, fig. 92. 1891. Type. Gard. Chron., ser. 3, 9: 435, fig. 92. 189 1. (lectotype) (Farjon and Styles 1997).
2. P. patula Schiede ex Schlechtendal et Chamisso var. longipedunculata Loock ex Martínez, Pinos Mexicanos, ed. 2, 333, figs. 276-280, 1948. Type Mexico, Oaxaca: Rancho Benito Juárez (Rancho Tablas), 1947.07, Loock 113a (holotype, PRF-n.v.; isotype, MEXU) (Farjon and Styles 1997).
Farjon and Styles (1997) provide the following notes on the history of the species and its varieties: "Schlechtendal and Chamisso (1831) gave under C.J.W. Schiede & F. Deppe 1108 a concise description of a 3-leaved pine, of which they had seen no cones ('strobilo . . . nobis deficiente') in the material presented to them. ... Gordon (1875) described Pinus patula (var.) macrocarpa based on collections by C.J.W. Schiede with a cone size 'from 6-7 inches long and 2 inches broad', which, if correct, would be quite outside the range of this species as here defined. Masters (1891) formally published this combination and provided an illustration of the cone. No specimen has been traced in the herbaria to match the descriptions and/or the illustration. The illustration in Masters (1891) is therefore designated as the lectotype. ... Martínez (1948) ascribed his new variety P. patula var. longipedunculata to Loock, who coined the name on the label of the type specimen. He described it as different from 'typical’ P. patula in having 2 resin ducts in the leaves instead of 3 and in having pedunculate (5–15 mm) cones versus sessile cones. Perry (1991) allows it occasionally 3 resin ducts."
Farjon and Styles (1997) also report that "Styles (1976) concluded that 'it agrees phenotypically in all botanical characters' with those mentioned by Martinez (1940) under P. oocarpa var. ochoterenae and synonymized both under P. patula. He later expressed a different view (Styles, 1984) but stopped short of formally synonymizing these two taxa under his newly created combination P. patula subsp. tecunumanii. From his determinations of specimens it appears that P. oocarpa var. ochoterenae Martínez was treated as a synonym of P. patula subsp. tecunumanii (see under P. tecunumanii), but that at least more-recently collected material (Higman, Padilla & Styles 40) was again accepted as P. patula (subsp.) longipedunculata. Observation in the field and study of type material by A. Farjon confirm recognition of this taxon as a variety if peduncle length is coupled with persistence and serotiny, which may point to different adaptive traits between the two taxa." Note that Furman et al. (1997) have used RAPD markers to show clear and substantial genetic differences between P. patula and P. tecunumanii, establishing the latter as a good species.
Closely related species include Pinus greggii, P. jaliscana, P. oocarpa, P. praetermissa, P. pringlei, and P. tecunumanii, all of which also are native to Mexico.
The tree grows to 40 m tall and 100 cm dbh, usually with a single, straight, slender trunk; in closed canopy stands, the depth of the conical or domed crown is ca. 33%. The Bark on young trees is thin, scaly, red-brown, with age becoming thick, dark grey-brown, rough and scaly with large elongated plates and deep longitudinal fissures. First-order branches are long, slender, spreading or slightly ascending; higher order branches are slender, drooping, the ultimate branches pendent. The shoots are rough and scaly when the leaf fascicles have fallen, yellow- to red-brown, foliage shoots with prominent, decurrent pulvini. Cataphylls subulate, recurved at apex, scarious, with erose-ciliate margins, brown, early deciduous. Vegetative buds oblong to cylindrical, the terminal bud 15–20 mm long, the laterals shorter, brown, not resinous; the scales spreading, subulate, ciliate at margins. Fascicle sheaths initially 20–30 mm long with 6-8 imbricate, chartaceous, white-yellow to orange-brown scales, persistent but shortening to 12–15 mm in mature fascicles, slowly weathering to grey-brown. Leaves in fascicles of 3-4(-5), in drooping tufts, typically in two rows on either side of the upturned shoot, persisting 2–3 years, thin, lax, drooping to pendent, (11-)15-25(-30) cm × 0.7-0.9(-1) mm, serrulate at the margins, acute, pale green to dark green. Stomata on all faces of the leaves, in 4-6(-7) lines on the convex abaxial face and 2-3(4) lines on each adaxial face. The leaves are triangular in cross section, the hypodermis usually with a double layer of cells; resin ducts (1-)2-3(4), medial, occasionally 1 internal, stele oval in cross section; outer walls of endodermal cells not thickened; vascular bundles 2, distinct, the xylem strands often connate. Pollen cones crowded near the proximal end of new shoots, spreading, subtended by scarious bracts, ovoid-oblong to cylindrical, 15-20 × 5–6 mm, pink-yellow, turning yellow-brown. Seed cones subterminal or lateral, in whorls of 2 to many, rarely solitary, persistent or deciduous, on short or moderately long (to 20 mm) peduncles. Immature cones ovoid, on short or long recurved peduncles with persistent cataphylls, purple turning light brown, maturing in two seasons. Mature cones narrowly ovoid when closed, usually slightly curved, more or less asymmetrical at base, 5-10(-12) × (3-)4-6.5 cm when open. Seed scales 100-150, serotinous or parting some time after maturing, tenacious or deciduous with the peduncle, (thin) woody, oblong, usually curved when spreading, the proximal scales connate, purple-brown to dark brown, with adaxial light brown marks left by seed wings. Apophysis nearly flat to slightly raised, transversely keeled, more or less gibbous on the proximal scales, more so on one side of the cone, rhombic, upper margin acute or obtuse-rounded, abaxial surface striate or smooth, (lustrous) ochraceous or yellow-brown. Umbo dorsal, flat or raised, often sunken into the apophysis, 3–7 mm wide, grey, with a minute, deciduous prickle. Seeds obliquely ovoid, flattened, 4-6 × 2–4 mm, dark gray. Seed wings articulate, held to the seed by two oblique claws which partly cover the seed on one side, obliquely ovate-oblong, 12-18 × 5–8 mm, light brown with dark stripes (Farjon and Styles 1997).
- "Mexican conifers in San Luis Province, Argentina".
- "RHS Plant Selector - Pinus patula". Retrieved 30 June 2013.
- Eguiluz T.1982. Clima y Distribución del género pinus en México. Distrito Federal. Mexico.
- Rzedowski J. 1983. Vegetación de México. Distrito Federal, Mexico.
- Richardson D.M. (Ed) 2005. Ecology and biogeography of Pinus. Department of Conservation. South Island Wilding Conifer Strategy. New Zealand.
- Chandler, N.G. Pulpwood plantations in South Africa. Proc. Aust. Paper Indus. Tech. Ass.
- Gutiérrez, Millán, W. Ladrach. 1980. Resultados a tres años de la siembra directa de semillas de Cupressus lusitanica y Pinus patula en finca Los Guaduales Departamento del Cauca. Informe de Investigación 60. Cali, Colombia. Cartón de Colombia S.A. 6 p.
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