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Image of Cedros Island Pine
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Cedros Island Pine

Pinus radiata D. Don

Associations

provided by BioImages, the virtual fieldguide, UK
Foodplant / saprobe
thinly subiculate apothecium of Arachnopeziza obtusipila is saprobic on dead twig of Pinus radiata
Remarks: season: 11-3

In Great Britain and/or Ireland:
Foodplant / saprobe
fruitbody of Basidiodendron pini is saprobic on dead, decayed wood of Pinus radiata

Fungus / saprobe
erumpent pycnidium of Camarosporium coelomycetous anamorph of Camarosporium pini is saprobic on fallen cone of Pinus radiata

Foodplant / saprobe
erumpent, solitary apothecium of Cistella acuum is saprobic on dead, especially still attached to cut off branches needle of Pinus radiata
Remarks: season: 9-3

Foodplant / saprobe
superficial perithecium of Coniochaeta malacotricha is saprobic on dead branch of Pinus radiata
Remarks: season: 3-6

Fungus / saprobe
subepidermal, then exposed apothecium of Cyclaneusma minus is saprobic on fallen needle of Pinus radiata
Remarks: season: 11-5

Foodplant / saprobe
colony of Dendrodochium anamorph of Dendrodochium citrinum is saprobic on dead cone of Pinus radiata
Remarks: season: 8-4
Other: minor host/prey

Foodplant / saprobe
apothecium of Dennisiodiscus pinicola is saprobic on cone of Pinus radiata
Remarks: season: 10-11
Other: minor host/prey

Foodplant / saprobe
fruitbody of Diplomitoporus flavescens is saprobic on fallen, dead trunk of Pinus radiata

Foodplant / saprobe
fruitbody of Exidia saccharina is saprobic on dead, fallen branch of Pinus radiata

Foodplant / saprobe
fruitbody of Exidiopsis effusa is saprobic on dead, decayed wood of Pinus radiata
Other: minor host/prey

Foodplant / pathogen
Brunchorstia anamorph of Gremmeniella abietina infects and damages live twig of Pinus radiata

Foodplant / saprobe
apothecium of Hyaloscypha aureliella is saprobic on wood of Pinus radiata
Remarks: season: 7-11

Foodplant / saprobe
erumpent, often clustered apothecium of Lachnellula subtilissima is saprobic on fallen twig of Pinus radiata
Remarks: season: 1-7

Foodplant / saprobe
thyriothecium of Lichenopeltella pinophylla is saprobic on dead, fallen needle of Pinus radiata
Remarks: season: 2-7

Foodplant / saprobe
thyriothecium of Microthyrium pinophyllum is saprobic on decaying needle of Pinus radiata
Remarks: season: 2-4

Foodplant / saprobe
toadstool of Mycena seynesii is saprobic on dead, fallen, decayed cone of Pinus radiata

Foodplant / pathogen
Dothistroma coelomycetous anamorph of Mycosphaerella pini infects and damages live needle of Pinus radiata

Foodplant / saprobe
stromatic, in large groups perithecium of Nectria fuckeliana is saprobic on dead twig of Pinus radiata
Remarks: season: 3-5, 9-12

Foodplant / saprobe
apothecium of Orbilia xanthostigma is saprobic on decorticate wood of Pinus radiata
Remarks: season: 1-12
Other: minor host/prey

Foodplant / parasite
fruitbody of Phellinus pini parasitises live trunk of Pinus radiata
Other: minor host/prey

Foodplant / mycorrhiza / ectomycorrhiza
fruitbody of Russula insignis is ectomycorrhizal with live root of Pinus radiata
Remarks: Other: uncertain
Other: minor host/prey

Foodplant / pathogen
erumpent pycnidium of Sphaeropsis coelomycetous anamorph of Sphaeropsis sapinea infects and damages live cone of Pinus radiata
Remarks: season: 10-4

Foodplant / saprobe
pycnidium of Sirothyriella coelomycetous anamorph of Stomiopeltis pinastri is saprobic on dead, fallen, rotting needle of Pinus radiata

Foodplant / secondary infection
erumpent pycnidium of Sclerophoma coelomycetous anamorph of Sydowia polyspora secondarily infects gall-midge infected needle of Pinus radiata

Foodplant / saprobe
fruitbody of Trechispora clancularis is saprobic on dead, decayed litter of Pinus radiata

Foodplant / saprobe
Tubulicrinis accedens is saprobic on dead, decayed wood of Pinus radiata

Foodplant / saprobe
Tubulicrinis chaetophorus is saprobic on dead, decayed wood of Pinus radiata

Foodplant / saprobe
Tubulicrinis subulatus is saprobic on dead, decayed wood of Pinus radiata
Other: minor host/prey

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Comments

provided by eFloras
Pinus radiata has an extremely narrow natural range: three coastal areas in California (one in San Mateo and Santa Cruz counties, one in Monterey County, and one in San Luis Obispo County) and off the coast of Baja California, Mexico (Guadalupe Island and debatably also on Cedros Island). Some natural populations of the species are under protection. Along the California coast it has escaped from cultivation, and from there into southern coastal Oregon it shows signs of naturalizing.

Pinus radiata is a much better-formed tree and of greater silvicultural value within its introduced range (Africa, Australia, Europe, and New Zealand, where it is a principal timber tree) than in its native range. It hybridizes naturally with P . attenuata ( P . ´ attenuiradiata Stockwell & Righter).

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Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of North America Vol. 2 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
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Description

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Trees to 30m; trunk to 0.9m diam., contorted to straight; crown broadly conic, becoming rounded to flattened. Bark gray, deeply V-furrowed, furrow bases red, ridges irregularly elongate-rectangular, their flattened surfaces scaly. Branches level to downcurved or ascending, poorly self-pruning; twigs slender, red-brown, sometimes glaucous, aging gray, rough. Buds ovoid to ovoid-cylindric, red-brown, ca. 1.5cm, resinous. Leaves (2--)3 in a fascicle, spreading-ascending, persisting 3--4 years, (8--)9--15(--20)cm ´ 1.3--1.8(--2)mm, straight, slightly twisted, deep yellow-green, all surfaces with fine stomatal lines, margins serrulate, apex conic-subulate; sheath (1--)1.5--2cm, base persistent. Pollen cones ellipsoid-cylindric, 10--15mm, orange-brown. Seed cones maturing in 2 years, shedding seeds soon thereafter, but often serotinous and persistent 6--20 years, solitary to whorled, spreading to recurved, curved, very asymmetric, ovoid before opening, broadly ovoid when open, 7--14cm, pale red-brown and lustrous, scales rigid, stalks to 1cm; apophyses toward outer cone base increasingly mammillate, those on inward cone side and middle and apex of cone more level; umbo central, mostly depressed, with small central boss or occasionally with slender, deciduous prickle. Seeds compressed-ellipsoid; body ca. 6mm, dark brown; wing 20--30mm. 2 n =24.
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cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of North America Vol. 2 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Flora of North America @ eFloras.org
editor
Flora of North America Editorial Committee
project
eFloras.org
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Habitat & Distribution

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Coastal fog belt; of conservation concern; 30--400m; Calif.; Mexico in Baja California [600--1200 m].
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copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of North America Vol. 2 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Flora of North America @ eFloras.org
editor
Flora of North America Editorial Committee
project
eFloras.org
original
visit source
partner site
eFloras

Synonym

provided by eFloras
Pinus insignis Douglas ex Loudon
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copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of North America Vol. 2 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Flora of North America @ eFloras.org
editor
Flora of North America Editorial Committee
project
eFloras.org
original
visit source
partner site
eFloras

Common Names

provided by Fire Effects Information System Plants
Monterey pine
insignis pine
radiata pine
Cambria pine
Guadalupe Island pine
Cedros Island pine
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Conservation Status

provided by Fire Effects Information System Plants
Information on state- and province-level protection status of plants in the
United States and Canada is available at NatureServe.
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Description

provided by Fire Effects Information System Plants
Monterey pine is a native, evergreen conifer. It attains a height of
49.5 to 115.5 feet (15-35 m) and a d.b.h. of 24 to 36 inches (60-90 cm)
[43]. The outer bark is narrowly ridged and the inner bark is resinous
[33,43]. The needles occur in clusters of three and are 4 to 6 inches
(10-15 cm) long. They persist for approximately 3 years [11,33,43].
Cones are 3 to 5.5 inches (7.5-14 cm) long and occur in one or more
clusters of three to five around the branch [16,33,43,54]. Monterey
pine lives a maximum of 80 to 90 years [49].

Monterey pine has a low frost tolerance [35].
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Distribution

provided by Fire Effects Information System Plants
The typical variety of Monterey pine occurs along the coast of
California in three disjunct populations in San Mateo and Santa Cruz
counties, Monterey County, and San Luis Obispo County. Pinus radiata
var. binata occurs on Guadalupe Island, Mexico [12,32,33,35,42]. Pinus
radiata var. cedrosensis is found on Cedros Island, Mexico [10,12,38].

Monterey pine is cultivated for timber in Maui, Hawaii [33]. It is also
widely planted for timber in Australia, New Zealand, South Africa,
Chile, Spain, and the British Isles [33,35,41,46,51].
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Fire Ecology

provided by Fire Effects Information System Plants
More info for the terms: fire regime, serotinous, surface fire

Monterey pine cones are serotinous; seeds are released when cones are
exposed to heat such as fire or high air temperature [19,31,37,53].
Fire is particularly effective for opening cones and releasing seeds.
It also creates a favorable seedbed. Reproduction rates are greatest
after surface fire in which the parent trees survive [52].

The foliage of Monterey pine is low in volatile terpenes [10].

FIRE REGIMES :
Find fire regime information for the plant communities in which this
species may occur by entering the species name in the FEIS home page under
"Find FIRE REGIMES".
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cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Fire Management Considerations

provided by Fire Effects Information System Plants
Thinning and pruning in Monterey pine plantations result in accumulation
of flammable fuels [8]. Crown scorch and cambium damage are reduced
when slash is mechanically reduced before burning [8].
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cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Growth Form (according to Raunkiær Life-form classification)

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More info on this topic.

More info for the term: phanerophyte

Phanerophyte
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Habitat characteristics

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More info for the term: tree

The climate where Monterey pine occurs is humid with mild year-round
temperatures. Winters are wet. Rain does not usually fall in July and
August, but tree crowns collect moisture from summer fog moving inland
[35]. On Guadalupe and Cedros islands the climate is mediterranean
[23,35].

Soils in which Monterey pine grows are often deep, sandy loams with a
clay layer 20 to 33 inches (50-80 cm) below the surface. Good sites
have a top layer of organic soil. Soils are generally acidic [35].
Slopes are typically gentle and often north facing [35].
license
cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Habitat: Cover Types

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More info on this topic.

This species is known to occur in association with the following cover types (as classified by the Society of American Foresters):

255 California coast live oak
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Habitat: Ecosystem

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More info on this topic.

This species is known to occur in the following ecosystem types (as named by the U.S. Forest Service in their Forest and Range Ecosystem [FRES] Type classification):

FRES28 Western hardwoods
FRES34 Chaparral - mountain shrub
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cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Habitat: Plant Associations

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More info on this topic.

This species is known to occur in association with the following plant community types (as classified by Küchler 1964):

More info for the term: forest

K009 Pine - cypress forest
K030 California oakwoods
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cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Immediate Effect of Fire

provided by Fire Effects Information System Plants
More info for the terms: crown fire, tree, wildfire

Monterey pine is killed by severe surface or crown fire. Trees survive
crown scorch unless it is extensive. In South Africa Monterey pine
survived a surface wildfire except where crown scorch was greater than
90 percent [13,14]. Trees are damaged by direct heat. Exposure to a
temperature of 424 degrees Fahrenheit (200 deg C) for more than half a
minute resulted in cambium death wherever heat was applied [13,52].
Such localized burning or scorching of bark of mature trees causes
scarring but may not result in tree death [52].

Young, thin-barked Monterey pine are often killed by fire, particularly
when stands are dense and crown fire occurs [52].
license
cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Importance to Livestock and Wildlife

provided by Fire Effects Information System Plants
Goats, black-tailed deer, and porcupine browse Monterey pine. Porcupine
also eat the bark [27,30,35]. Birds and small mammals consume the seeds
[35].
license
cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Key Plant Community Associations

provided by Fire Effects Information System Plants
More info for the terms: cone, natural, woodland

Monterey pine is part of the coastal closed-cone coniferous woodland
[23]. It is named as a dominant canopy member in the following
publications:

Terrestrial natural communities of California [23]
A vegetation classification system applied to southern California [44]
Vascular plant communities of California [50]
The closed cone pines and cypress [52]

Associated trees not mentioned in distribution and occurrence are Gowen
cypress (Cupressus goveniana var. goveniana), Monterey cypress (C.
macrocarpa), Santa Cruz cypress (C. goveniana var. abramsiana), Tecate
cypress (C. guadalupensis var. forbesii), bishop pine (Pinus muricata),
and Pacific madrone (Arbutus mensiesii) [23,36,50,52]. Understory
associates include woolyleaf manzanita (Arctostaphylos tomentosa),
California huckleberry (Vaccinium ovatum), poison-oak (Toxicodendron
diversiloba), El Dorado bedstraw (Galium californicum), thingrass
(Agrostis diegoensis), and blue wildrye (Elymus glaucus) [23,52].
license
cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Life Form

provided by Fire Effects Information System Plants
More info for the term: tree

Tree
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cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Management considerations

provided by Fire Effects Information System Plants
More info for the term: natural

Cone processing and nursery practices are discussed in the literature
[11,25].

Monterey pine is affected by many pests such as western dwarf mistletoe,
western gall rust, various needle blights, and moths [2,35,44].

Monterey pine is moderately windfirm on deep soils [35].

Goats have nearly eradicated all natural regeneration of Montery pine on
Gudalupe Island [27,35].

Much of the Monterey pine planted as ornamentals comes from New Zealand
stock. This stock originated from native California populations several
generations ago. In Cambria and Monterey, California, this imported
stock is crossbreeding with native individuals. The genetic effects of
this crossbreeding on native trees is unknown, and preserving genotypes
of native individuals is a point of management concern [39]. Monterey
pine is the subject of a genetic conservation program [27].
license
cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Occurrence in North America

provided by Fire Effects Information System Plants
CA HI MEXICO
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Other uses and values

provided by Fire Effects Information System Plants
Monterey pine is valued for shade and as an ornamental [33,35]. It
provides a barrier to wind and noise [35,53]. It is also used for
Christmas trees [35].
license
cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Phenology

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More info on this topic.

Pollination occurs from January to February but may be extended due to
high temperatures [15,25,35]. Cones open and seeds are dispersed in the
first warm, moist days of late winter and early spring. Cones may open
and close several times as moisture and temperature conditions fluctuate
[35].
license
cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Plant Response to Fire

provided by Fire Effects Information System Plants
More info for the terms: density, seed, wildfire

Monterey pine cones open and release seed after fire [19]. In
California, White [in 52] reported a seedling density of 196 per acre
(490/ha) the January following a spring wildfire. Seedlings were 12 to
22.4 inches (30-56 cm) tall.
license
cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Post-fire Regeneration

provided by Fire Effects Information System Plants
More info for the terms: crown residual colonizer, root crown

Tree without adventitious-bud root crown
Crown residual colonizer (on-site, initial community)
license
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Regeneration Processes

provided by Fire Effects Information System Plants
More info for the terms: cone, seed

The minimum seed-bearing age for Monterey pine is between 5 and 10
years. Maximum seed production beings at 15 or 20 years of age if trees
are open-grown, and later if stands are dense [11,25,35]. Cones are
produced annually, with good cone crops produced every other year [25].
Mature cones remain attached to the branch. They may remain closed for
several years, depending upon temperature and humidity. Cones open and
release seed during warm, dry periods and close rapidly when temperature
drops and relative humidity increases. This results in a constant but
meager seed rain [52]. The cones of native populations open
infrequently because their habitat is typically cool and moist.
Seedfall is heaviest in warm, dry years [35]. Unreleased seed remains
viable for decades. Seeds from cones up to 24 years of age have
germinated; however, germinative capacity appears to fall off with
progressing years [52]. Seeds can be exposed to a temperature of 203
degrees Fahrenheit (95 deg C) before germination is significantly
reduced [29]. Seedling recruitment is best on mineral soil [52].
Details of growth are discussed in the literature [11].

Monterey pine does not reproduce by sprouting [14,35].
license
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Regional Distribution in the Western United States

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This species can be found in the following regions of the western United States (according to the Bureau of Land Management classification of Physiographic Regions of the western United States):

3 Southern Pacific Border
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Successional Status

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Facultative Seral Species

Monterey pine normally invades dry sites with poor, shallow soils. It
also invades oldfields after land clearance, grazing, fire, or logging
[48]. Trees establish in even-aged stands [52].

Monterey pine has intermediate shade tolerance [6,35]. As it matures it
becomes even less tolerant of shade, and shows optimal growth in full
sunlight [5].
license
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Synonyms

provided by Fire Effects Information System Plants
Pinus insignis Dougl. ex Loud.
Pinus muricata D. Don var. cedrosensis Howell
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Taxonomy

provided by Fire Effects Information System Plants
The currently accepted scientific name of Monterey pine is Pinus radiata
D. Don [12,31,32,33,43]. There are three recognized varieties [10,38]:

Pinus radiata var. radiata
Pinus radiata var. binata Lemmon
Pinus radiata var. cedrosensis (Howell) Axelrod.

Monterey pine hybridizes with knobcone pine (Pinus attenuata) and bishop
pine (Pinus muricata) [12,32,25].
license
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Value for rehabilitation of disturbed sites

provided by Fire Effects Information System Plants
Monterey pine is planted for erosion control [35]. Ease of
establishment and a widespreading root system make it a good species for
stabilizing soils on steep slopes [28].
license
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bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Wood Products Value

provided by Fire Effects Information System Plants
Monterey pine wood is light, soft, and coarse grained [35,43]. It is of
little commercial value in the United States except as fuelwood [35].
In other parts of the world it is used for general construction,
flooring, furniture, joinery, plywood, reconstituted panel products, and
paper. When treated with preservatives it cab be used for siding,
decking, external trim, poles, piles, fencing, and railroad ties [4].
license
cc-publicdomain
bibliographic citation
Cope, Amy B. 1993. Pinus radiata. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/

Associated Forest Cover

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Monterey pine has been listed in at least two vegetation classifications: the Closed-Cone Pine Forest Community of California (27) and the Closed-Cone Pine and Cypress Californian Floristic Province (31).

The fossil record, although somewhat limited, indicates that this pine once occupied a larger range during the late Pleistocene epoch, extending almost continuously along the outer coastal strip and California islands. Fossil remains have been found at Tomales Bay, Little Sur, Carpinteria, Rancho La Brea, and Santa Cruz Island. The evidence suggests that present-day pines are survivors of an ancient oak-laurel, pine, and palm forest that grew well in a mild climate (2).

Fire is a major influence affecting the extent and makeup of Monterey pine stands. Fire is frequent, sometimes of natural causes, often accidental, and sometimes deliberately set. Graziers at Cambria, for example, burned the woods to obtain more grass. At Año Nuevo, frequent fires have helped to maintain the pine forest. Without fire, the taller and longer-lived coast Douglas-fir (Pseudotsuga menziesii var. menziesii) would usurp land occupied by pines. Much regeneration and a number of even-aged stands at all three mainland locations can be traced directly to the influence of fire.

Many of the plant species associated with Monterey pine have been listed (32). Such lists are subject to change because undisturbed stands are scarce; nearly all have been grazed, burned, or logged.

At Año Nuevo, tree associates of Monterey pine are coast Douglas-fir, redwood (Sequoia sempervirens), knobcone pine (Pinus attenuata), ponderosa pine (P. ponderosa var. ponderosa), coast live oak (Quercus agrifolia), and Pacific madrone (Arbutus menziesii). Some portions of the Monterey pine forest are pure and almost fully stocked with 370 to 740 trees per hectare (150 to 300/acre). Width of tree crowns varies with age, but rarely are crowns interlocking. Monterey pine also intermingles with Douglas-fir on middle slopes and with knobcone pine and an occasional ponderosa pine on upper drier slopes, especially where the soil is shallow and rocky. On lower slopes, redwood and an occasional madrone are present. Coast live oak, usually in the understory, also is an associate species. In some places, natural regeneration of Monterey pine is prominent, particularly where disturbance has bared the soil.

Understory associates generally are not particularly diverse nor abundant at Año Nuevo. In places, however, understory vegetation fully occupies the ground. In addition to young coast live oak, the most common species are bracken (Pteridium aquilinum), poison-oak (Toxicodendron diversilobum), coyotebrush (Baccharis pilularis), blueblossom (Ceanothus thyrsiflorus), California buckthorn (Rhamnus californica), blackberry (Rubus spp.), coast sagebrush (Artemisia californica), and several grasses.

At Monterey, tree associates are coast live oak, Monterey cypress (Cupressus macrocarpa), Gowen cypress (C. goveniana), and bishop pine (Pinus muricata). Coast live oak is the most common tree associate of Monterey pine. Seldom taller than 9 m (30 ft), the oak usually is relegated to the understory. White alder (Alnus rhombifolia) and a species of willow (Salix sp.) are occasional associates in riparian zones. At least one species of willow is scattered throughout the forest on higher ground.

Shrubs and forbs in the Monterey forest vary with time after disturbance and general quality of the habitat. Successionally, young stands of pines, shrubs, and forbs often become established after fire.

At age 45, Monterey pine has a stand density of 160 to 200 trees per hectare (65 to 81/acre). Shaggy-bark manzanita (Arctostaphylos tomentosa) and California huckleberry (Vaccinium ovatum) are prominent with an average cover of about 50 percent. By the time Monterey pine reaches age 65, competition, disease, and slow growth reduce its density to 80 to 120 trees per hectare (32 to 49/acre). In stands of this age, poison-oak, bush monkeyflower (Mimulus aurantiacus) and California blackberry (Rubus ursinus) are present and, along with the shrubs mentioned earlier, contribute to a shrub cover of about 40 percent. Openings form in the pine stand as the trees grow older but density remains about as before because younger age classes of pines contribute. Shrub cover continues at about 40 percent with poison-oak and creeping snowberry (Symphoricarpos mollis) becoming the understory dominants. In old stands where tree diameters are over 100 cm (39 in), one or more age classes of pine are present. Coast live oak sometimes constitutes 25 to 50 percent of the trees in such stands (37).

At Cambria, tree associates of Monterey pine are limited to one hardwood: coast live oak. On better sites, understory vegetation near the typically open pine stands includes coast live oak, bracken, California blackberry, and poison-oak. On drier sites, coast sagebrush, coyotebrush, and bush monkeyflower are present. At the edge of the pine's natural range, grasses often are the only understory plants.

On Guadalupe and Cedros Islands, vegetation associated with Monterey pine is poorly known. That reported for Guadalupe Island is island live oak (Quercus tomentella), Guadalupe Island palm (Erythea edulis), and grasses; for Cedros, bishop pine, yucca (Yucca spp.), and at least two species of cactus (Opuntia spp.).

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Climate

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The Monterey pine habitat is strongly influenced by its proximity to the Pacific Ocean from which the cold waters of southward-flowing currents result in high humidity, low temperatures, and summer fogs. The minimum relative humidity at Monterey in July, for example, averages between 60 and 70 percent (23). At least one-third of the days each year are foggy (35).

Temperatures tend to be mild, although extremes range from about -5° to 41° C (23° to 106° F). Mean monthly temperatures show a relatively even climate with a difference between the coldest and warmest month of about 6.5° C (12° F) in the range of 9° to 11° C (48° to 52° F) in winter and 16° to 18° C (61° to 64° F) in summer. Mean temperatures during the growing season, February through June, range from 11° to 16° C (52° to 61° F), with maximums of 17° to 24° C (63° to 75° F) (34). Frost-free days number about 300 each year.

Annual precipitation ranges from about 380 to 890 mm (15 to 35 in) and varies from year to year. From December to March, precipitation averages 300 to 510 mm (12 to 20 in), with less than 50 mm (2 in) per month for the remaining months. Rain usually does not fall in July and August. During these months, however, the tree crowns collect moisture from fog that moves inland. Fog drip can amount to as much as 15 mm (0.59 in) per week at higher elevations on the Monterey Peninsula (25). No snow falls in the natural range of Monterey pine. Año Nuevo is the wettest of the three mainland locales; Cambria, the driest; and Monterey, the foggiest (3).

Wind is, at best, a minor climatic influence, averaging only 7.6 km/h (4.7 mi/h) on an annual basis. May is the windiest month, August the least windy (23).

The climate of Guadalupe and Cedros Islands is Mediterranean-like, possibly with less rainfall and greater temperature extremes than for mainland stands. Fog is a critical factor and, on both islands, pine stands are restricted to foggy ridges and windward slopes, or occasionally to the moist slopes of deep canyons. On Cedros Island, fog was most frequent and of maximum concentration where the pines grew, and each pine grove tended to be covered with fog while the desert between was exposed to clear sky (22).

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Damaging Agents

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Within its restricted range, few abiotic factors cause significant damage except pollution, especially ozone. Because of its rapid growth, Monterey pine has been planted widely along the western coast of North America. In these plantings and even in the Central Valley of California, the pine technically is an introduced species because it is exposed to environmental conditions rare in its native range. Temperatures below freezing for only a few hours seriously damage and kill trees of all ages. Trees that are rapidly growing or newly planted are susceptible to windthrow during winter storms. Sudden increases in temperature to 38° C (100° F) or greater cause needle scorch and damage to new growth (5).

Fire is a particular hazard to young, thin-barked trees and can be disastrous in dense plantations where persistent lower limbs become festooned with dead needles, resulting in an ideal situation for crowning fires. Pruning to a height of 2.1 to 2.4 m (7 to 8 ft) helps keep a fire on the ground and is a desirable measure for protection (32).

Pathogens of significance in the natural range of Monterey pine include a dwarf mistletoe, two gall rusts, and two root diseases. Digger pine dwarf mistletoe (Arceuthobium occidentale) infects trees of all ages and is found in native stands except at Aho Nuevo (32). Western gall rust (Peridermium harknessii) and coastal gall rust (P. cerebroides) are found in the three stands in the United States and cause significant damage to young trees. Cedros and Guadalupe Island populations of Monterey pine have higher resistance to western gall rust than mainland populations (29). A widespread pathogen of particular virulence is annosus root disease (Heterobasidion annosum). Armillaria root disease (Armillaria mellea) is found where oaks are present, but damage to Monterey pine is minor.

Outside its natural range, Monterey pine is attacked by several pathogens in addition to those in native stands. Of these, the red band needle blight (Scirrhia pini) is the most damaging. This worldwide pathogen is not found in native stands but has caused serious damage and is a major concern for plantations in British Columbia, Washington, Oregon, and north-coastal California. Western gall rust is a pest in plantations from central California to British Columbia and can be damaging to Christmas tree plantations. As many as 35 other pathogens cause negligible to minor damage in exotic stands of Monterey pine (5,32).

Furniss and Carolin (12) list 56 insects from 44 genera that feed on Monterey pine foliage, twigs, branches, and boles. Relatively few of these cause significant damage and only five can kill trees, especially those weakened by other agents. Four are bark beetles and one is a weevil; all are cambium feeders.

Bark beetle larvae mine the cambium of all but young trees. Once the trunk is girdled, the tree dies. All four species produce broods in stumps or fresh cut limbs and logs and commonly work in concert on individual trees. The Monterey pine ips (Ips mexicanus) is seldom a primary killer except in young plantations. The California four-spined ips (I. plastographus) and pinyon ips (I. confusus) attack large and small trees. The red turpentine beetle (Dendroctonus valens) killslarge, mature trees.

The Monterey pine weevil (Pissodes radiatae) is primarily a threat to young trees where the larvae mine cambium in tops, stems, bases, and even portions below ground.

Various other insects, including aphids, borers, caterpillars, and moths, cause minor damage. Probably the most serious of these is the Monterey pine cone beetle (Conophthorus radiatae) that attacks maturing cones in central California but does not damage the more southerly population.

Animal damage to ornamental plantings can be a problem but generally is not serious. On Guadalupe Island, however, chronic overgrazing by goats has virtually eliminated Monterey pine regeneration.

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Flowering and Fruiting

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In its native habitat, Monterey pine "flowers" in late winter and early spring. The species is monoecious; the numerous yellow male strobili are produced on side branches, and female flowers are produced in all parts of the crown. Monterey pine is multi-nodal and female strobili occasionally are found at a secondary whorl position (18).

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Genetics

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Population Differences The three mainland populations of Monterey pine, although disjunct, grow where climate and soil are similar. A large proportion of the total phenotypic variation in several branch, needle, and cone characteristics, however, is observed between individual trees at each location. The Cambria population, although less variable than the other two, differs from them in several cone, branch, and needle characteristics. In Australia these differences, plus a slower growth rate and a different pattern of seasonal growth, suggest that the Cambria population differs genetically from the northern populations (11). A recent study, however, indicates little genetic differentiation among the native populations. Most of the genetic variation is located within each stand (26).

Hybrids No evidence of widespread introgression from knobcone or bishop pine has been found, although hybridization is occurring locally between Monterey and knobcone pines at Año Nuevo (11). The hybrid is designated Pinus attenuata x radiata Stockwell & Righter. The two-needled pine found on Guadalupe and Cedros Islands is currently named P. radiata var. binata.

The unique characteristics of rapid growth, large genetic variability, and ease of vegetative propagation have made Monterey pine the subject of intensive genetic improvement programs in several countries, notably Australia and New Zealand.

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Growth and Yield

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On good sites, pine saplings that are free to grow and have at least moderate spacing enlarge rapidly: an increase in height of 1.2 to 2.4 m (4 to 8 ft) per year has been observed (23). By age 15, trees are 24 cm (9.4 in) in d.b.h. and 16 m (53 ft) tall (19). These values indicate a growth rate for the first 15 years that places Monterey pine among the most rapidly growing of American conifers. Although reproduction can be very dense, stands seldom, if ever, stagnate. A few saplings grow faster than their counterparts, quickly establish dominance, and eventually form the well-spaced, relatively open stands typical of older Monterey pine forests.

Branches of Monterey pine saplings die when shaded but persist on the bole for many years. In dense stands, the trunks clean themselves well (35). Mature trees often have clear boles for 8 to 15 m (26 to 49 ft).

Height growth of pole-sized trees on poor sites may slow down appreciably after 15 years, but on better sites, it continues at a good rate until trees are about age 50 (19). At Monterey, pole-sized trees less than 30 cm (12 in) in d.b.h. average about 20 years old and 20 m (64 ft) tall. Height of mature trees ranges from 9 to 38 m (30 to 125 ft) but generally is 21 to 30 m (69 to 98 ft), with the tallest trees often found in small gullies. Diameters vary widely and, on a good site, average just under 64 cm (25 in) in d.b.h. A few trees reach an exceptional diameter of 122 cm (48 in) in d.b.h. At Cambria, Monterey pines are a little taller, averaging 30 to 37 m (98 to 121 ft) at maturity (23).

On Guadalupe Island, the tallest tree was 33 m (108 ft); the largest d.b.h. recorded was 211 cm (83 in). On Cedros Island, the tallest tree measured 32 m (105 ft); the tree with the largest d.b.h. was 77 cm (30 in) (21).

Crown development of Monterey pine is a function of age and spacing. In crowded conditions, the species has a narrow pointed crown. Vigorous trees continue to have pointed crowns until 35 to 45 years of age, after which the crown becomes flat and irregular. Trees 30 to 46 cm (12 to 18 in) in, d.b.h. have crowns 5 to 6 m (16 to 20 ft) wide, but much narrower if crowded, and those larger than 76 cm (30 in) in d.b.h. have crowns 9 to 12 m (30 to 39 ft) wide. Trees taller than 30 m (98 ft) have a live crown one-third to one-sixth of this length (23).

Monterey pine is short lived. It attains full size in 80 to 100 years and rarely lives beyond 150 years (35).

Yield of Monterey pine in natural stands is lowered by the characteristically open spacing of the trees. Pine volume averages less than 281 m³/ha (4,011 ft³/acre). As stocking increases, so does productivity. A stand with better than average stocking, for example, averaged 490 m³/ha (7,003 ft³/acre). Trees were about 50 years old, 39 cm (15 in) in d.b.h., and numbered 408/ha (165/acre). The best stocked stand at Monterey contained 482 trees and 1681 m³/ha (195 trees and 24,009 ft³/acre). These trees averaged 52 cm (20 in) in d.b.h. and 29 m (95 ft) in height (19).

In other countries, the yield of Monterey pine in plantations that are thinned and pruned and sometimes fertilized is much higher than that of natural stands. In New Zealand, stands 35 to 40 years old yield about 770 m³/ha (11,004 ft³/acre). On a productive site in Chile, trees 20 years old produce about 500 m³/ha (7,145 ft³/acre). They number about 270 trees per hectare (109/acre) after three thinnings, average about 48 cm (19 in) in d.b.h., and have been pruned three times (30).

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Reaction to Competition

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Because Monterey pine exists both as an overstory and an understory tree, it is classed as intermediate in tolerance to shade (4)- that is, at least as tolerant as any other pine in western North America. Age and site quality, however, affect this assessment. As a sapling or seedling, the species tolerates shade but becomes less tolerant in the pole stage and is intolerant when mature (19). When overtopped, young pines can withstand a considerable amount of suppression, struggling along for 30 years or more before they die.

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Rooting Habit

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After age 5, the roots of pine seedlings grow downward as far as soil depth or the clay layer permit. Main support roots, however, develop in the top 61 cm (24 in), even in deeper soils (23). Studies at Monterey and Cambria showed at least a few pine roots penetrated to 1.7 m (5.5 ft) in deeper soils (8,10). The root system becomes extensive laterally and roots of mature pines extend from 9 to 12 m (30 to 39 ft) from the tree (19). Where a layer of organic matter covers the soil, large numbers of small pine roots exploit the layer for moisture and nutrients.

The species is regarded as moderately windfirm on deeper soils but less so on shallow soils. Trees growing in soils saturated with moisture are vulnerable to windthrow, particularly in exposed places (24).

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Seed Production and Dissemination

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Fertile cones are produced as early as 5 to 10 years, but substantial crops are not yielded until age 15 or 20 if the trees are open-grown, and considerably later if the stands are dense. Cones mature in the autumn of the second season and most open during the first warm days of late winter and early spring. They range in color from lustrous nut brown to light brown when ripe, and in length from 8 to 18 cm (3 to 7 in). The ellipsoid seeds, jet black and pimpled, average about 2 cm (0.8 in) long. Monterey pines at Cambria have the largest cones and seeds; those at Monterey the smallest (11). Each cone contains from 120 to 200 seeds.

Cones remain attached to the trees for many years and open and close several times, depending on temperature and humidity. Because the habitat of the species is typically cool and moist, cone opening is infrequent and of short duration, so that seeds are often retained and then disseminated over a longer period than in warmer and drier climates.

Although cones and seeds are produced almost every year, seedfall varies. A relatively small number of seeds dribble out of the cones each year. In warm and dry years, seedfall can be heavy. Fire is particularly effective for opening cones and releasing large quantities of stored seeds.

Several species of birds and small mammals depend in part for sustenance on the seeds of Monterey pine. Principal bird species are the scrub jay, Stellar jay, and common crow. Important small mammals are deer mice, chipmunks, and ground squirrels (7). Numerous other creatures eat the seeds of this pine, but their effect usually is insignificant.

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Seedling Development

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Although the seeds of Monterey pine do not require stratification for good performance, germination is enhanced by it. Cold-moist stratification of 0 to 7 days is recommended for fresh seed and 7 to 20 days for stored seed. In one test with no pretreatment of seed, germinative energy was 16 percent in 7 days and germinative capacity 81 percent after 25 days at a controlled temperature of 20° C (68° F). In another test, again with no pretreatment, but where the day temperature was held at 30° C (86° F) and the night temperature at 20° C (68° F), germinative capacity was 67 percent after 28 days (18).

Germination is epigeal New germinants bear a whorl of five to nine cotyledons that are succeeded by primary needles. Secondary needles in fascicle bundles form when the seedling is a few months old. After age 3, the seedling produces only secondary needles. The root system of most seedlings consists of a slender taproot, aimed straight down.

Mycorrhizal associations with root tips in the upper 10 cm (4 in) of soil probably increase nutrient and water intake and enhance the growth of Monterey pine seedlings. At least 16 mycorrhizal fungi associated with Monterey pine have been identified in the United States and several others noted in other countries (28).

The seedbed required for natural regeneration of Monterey pine is highly variable. The best seedbed is moist mineral soil free of competing vegetation. Numerous seedlings, however, are found where the seedbed consists of several inches of pine needles over mineral soil (23). Although unknown, these seedlings could be the survivors of a great many seedlings and they could be much older than similar-sized, free-to-grow counterparts on bare mineral soil.

Seedlings develop best in full sunlight. Soil disturbed by logging and fire is conducive to seedling establishment and rapid growth. Dense slash decreases seedling density, although light slash can improve the seedling "catch."

Optimum conditions for regeneration, however, are produced by fire; maximum numbers of cones are opened, and at least a temporarily competition-free and receptive seedbed is prepared (37). As a result, dense stands often are formed after burning. In fire-killed stands in foreign countries, Monterey pine seedlings were reported to number 1,235,500/ha (500,000/acre) and more than 2,471,000/ha (1,000,000/acre) (32).

On Guadalupe Island, seedlings and saplings are scarce. "Very dense reproduction," however, was recorded in places on Cedros Island (21).

Pines also become established in grassland vegetation and beneath live oaks, the latter providing shade during the critical establishment period. In most instances, the pines eventually grow through the oak canopy and dominate (23). Some pines reproduce naturally under the canopies of older trees. Number and vigor of pine seedlings and saplings relate directly to the spacing of the older trees; the more dense the overstory, the fewer and slower growing the seedlings. Dense thickets often are formed in small openings.

Naturally established Monterey pine seedlings are fairly large initially and grow larger quickly. Seedlings 30 to 56 cm (12 to 22 in) tall after one growing season are common. Rapid shoot growth usually starts in February and continues until September. Monterey pine apparently begins growth at colder soil temperatures than associated conifers. Lack of soil moisture limits growth in the fall. The period of growth is variable, differing from tree to tree and from season to season (23). By age 5, trees are about 6.6 cm (2.6 in) in d.b.h. and 6 m (20 ft) tall (19). By this age, seedling roots have expanded much more laterally than vertically and have formed a lateral, rather than a taproot, system.

Artificial regeneration of Monterey pine in California is usually for horticultural rather than timber-growing purposes; however, several large plantations have been established for a variety of reasons. The most successful and long-lasting plantations are in central California near the Pacific Ocean (28).

Monterey pine grows readily in California nurseries. Its only problem is rapid growth and stock too large for field planting. At one nursery, average seedling height was 41 cm (16 in), accumulating from the normal seeding date in April to lifting in January.

Seedling size and growth are affected by seed size, soil temperature, and soil moisture. After 32 weeks, Monterey pine seedlings were taller and heavier from seeds retained by a 0.39 cm (0.15 in) mesh screen than from seeds passing through a 0.33 cm (0.13 in) screen (13).

Seedling root growth was greatest at 15° C (59° F), a value 5° C (9° F) lower than the optimum soil temperature reported for other pines. Monterey pines with a predawn water potential of -1.5 MPa (-15 bars) were unable to open stomates, a phenomenon also noted at a similar value for ponderosa and lodgepole (Pinus contorta) pines (17).

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Soils and Topography

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In spite of a small and narrow natural range, Monterey pine grows on soils that are derived from a variety of parent materials. At Año Nuevo, for example, the underlying rocks are shales and marine sandstones. At Monterey, these rocks and granite are present, and at Cambria, parent materials are limestones, sandstones, cherts, and slates.

Monterey pine is found on soils of four orders. Mollisols are the most prominent and include four Haploxerolls (Santa Lucia, Ben Lomond, Catelli, and Baywood soil series) (36) and four Argialbolls (San Simeon, Conception, Watsonville, and Chamise series). Ultisols are next in extent and are represented by an Albaquult (Narlon series). The Entisol order is represented by one soil series, a Xeropsamment (Tangair series), and the Alfisol order by a Palexeralf (Tierra series).

At all three locations-Año Nuevo, Monterey, and Cambria-the soils have a number of similarities. Most soils are deep sandy loams, often derived from marine sediments. A thick accumulation of organic material is common beneath Monterey pine stands on good sites. The 8- to 15-cm (3- to 6-in) layer of organic material stores many times its weight in water and is a modest reservoir for nutrients. Most soils are found on sloping ground and are reasonably well drained, at least down to a clay layer at the 50- to 85-cm (20- to 33-in) depth. The clay layer is of critical importance. Pine roots generally do not extend far into this layer, but many penetrate for a short distance. Such roots have been observed to be well inoculated with mycorrhizae (10). Another common attribute of soils supporting Monterey pine is that soil pH generally is acid, even extremely acid. Acidity often is high at or just above the clay layer. The combination of poor drainage and high acidity seems to enhance mycorrhizal formation. The clay layer, then, intercepts winter rains and forms a reservoir of water that is available for most of the year. Mycorrhizae on roots at or in the clay layer enhance the nutrient- and water-gathering capability of the pines. Of the seven most common mycorrhizal species that colonize the roots of Monterey pine seedlings in nurseries, Rhizopogon rubescens and R. luteolus enhanced height growth and nutrient uptake the most (6).

In general, the topography on which Monterey pine grows is hilly and gently to moderately sloping. With one possible exception in the Santa Lucia Mountains, elevations range from sea level to about 305 m (1,000 ft). At the three mainland elevations, the most extensive stands are found on modest slopes or gently rolling terrain between the ocean and steeper inland hills. The pine is found on north aspects at all locations and shifts from all aspects at Año Nuevo, through presence only in sheltered canyons on south aspects at Monterey, to complete absence on all other aspects at Cambria. On Guadalupe and Cedros Islands, stands are found on gentle to steep slopes at elevational ranges of 300 to 1100 m (980 to 3,610 ft) on Guadalupe, and 275 to 640 m (900 to 2,100 ft) on Cedros (21).

Limitations in habitat at each location probably contribute to the areal extent of the Monterey pine stands. At Año Nuevo, shallow soil near the coast could be limiting. At Monterey, lower rainfall together with differences in soil depth, texture, and location of clay layer could govern distribution. At Cambria, climate and soil mandate a shift from trees to grass and shrubs. Among the three mainland areas, where genetically controlled differences in tolerance to cold have been noted, the tolerance decreases from north to south (16). Recently, analyses of satellite photos taken over several years have shown that the present groves of closed-cone pines "are all at centers of high fog concentrations" (3). For the three mainland areas, the factor limiting the natural range of Monterey pine at its eastern boundary could be fog, but fog does not sufficiently explain the abrupt northern and southern termination of the pines' natural range. Farther south on Guadalupe and Cedros Islands, absence of fog appears to limit the distribution of the species. In spite of these evident limitations, the causes of restrictions on the range of Monterey pine are not clear.

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Special Uses

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The wood of Monterey pine is light, soft, brittle, and coarse-grained. The trunk is characterized by a large amount of crook and other irregularities, a small percentage of clear bole, and frequent presence of disease. These characteristics cause the species to be of little commercial value for lumber and wood products in the United States. Past commodity use has been for coarse lumber in a localized market and for fuelwood. In marked contrast, the species is valued for wood products in many other countries.

A major use of this pine is as an ornamental in parks and urban areas. The species often is planted in areas devoid of trees where its rapid growth and attractive foliage quickly provide variety and contrast to the landscape. The pine also is planted extensively to help establish vegetative control of eroding and blowing soils. Prized as a living screen against wind, noise, and traffic, Monterey pine graces many a boulevard and backyard in urban areas. It also has been asexually propagated for Christmas trees (33).

In its native habitat and particularly near the ocean, the rugged, picturesque, wind-battered trees deserve special mention for their esthetic appeal. Stands near Carmel, CA, are among the most photographed in the world.

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Vegetative Reproduction

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Monterey pine does not reproduce naturally from sprouts, and no record of sprouting in natural stands is known.

Reproduction from artificially rooted propagules of this pine has been successful in many trials in several countries. Hedging is one method for successfully mass-producing large numbers of symmetrical and straight cuttings and maintaining the juvenile nature of propagules (22). Plantlets from embryos and cotyledons are another (1).

Cuttings, or other means of vegetative propagation, offer a number of advantages over seedlings, not the least of which is closer control of genotype. Cuttings from mature planting stock show a reduced incidence of retarded leaders, excessive branching, crooked internodes, and frost susceptibility. Vegetative propagules also tend to have straighter boles, less forking, fewer and smaller branches, less bole taper, and thinner bark (22). Height growth of cuttings generally is similar to that of seedlings, although extremes of environment and age of ortet can cause lower growth than from seedlings. Cuttings also develop a higher frequency of cones on the bole-a negative factor. This can be mitigated by pruning, however.

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Distribution

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Native stands of Monterey pine are found in three distinct areas of central-coastal California in San Mateo, Santa Cruz, Monterey, and San Luis Obispo Counties. The northernmost stand is east of point Año Nuevo, the central stand 48 km (30 mi) to the south near Monterey and Carmel, and the southernmost stand about 105 km (65 mi) away in the Pico Creek-Cambria area (15). Seldom is the pine found more than 11 km (7 mi) from the sea. The north-south range is about 209 km (130 mi). A close relative of Monterey pine also inhabits the northeastern portion of Guadalupe Island and the northern and central parts of Cedros Island-both of which are Mexican possessions. Guadalupe Island is 740 km (460 mi) south of Cambria, and Cedros Island is 908 km (564 mi) south-southeast of Cambria. Although trees on these islands differ in morphology from those in the United States, they have now been shown to be most closely related to P. radiata (21).

The area occupied by natural stands of Monterey pine on the United States mainland was once well defined, even though estimates of the total area ranged from 4860 to 6480 ha (12,000 to 16,000 acres) (28). Precise natural limits, however, are now difficult to determine because of conspicuous amounts of new regeneration. The southern part of the forest at Año Nuevo, for example, is estimated to have increased by as much as 95 ha (235 acres) in recent decades (14). Additional trees have been planted, and these also have produced seed that led to many acres of new reproduction. Nevertheless, the total area currently occupied probably is no more than 8000 ha (19,770 acres) (21).


- The native range of Monterey pine.

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Brief Summary

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Pinaceae -- Pine family

Philip M. McDonald and Robert J. Laacke

Monterey pine (Pinus radiata) is the most widely planted pine in the world (9). Rapid growth and desirable lumber and pulp qualities cause it to be the leading introduced species in Australia, New Zealand, and Spain (34), and a major species in plantations of Argentina, Chile, Uruguay, Kenya, and the Republic of South Africa. In these countries, Monterey pine is a mainstay of the forest economy, serving internal markets, generating valuable foreign exchange reserves as an export, and reducing cutting pressure on native forests.

Pinus radiata was first noted by Thomas Coulter at Monterey, CA, in 1830. The scientific name refers to the strong markings on the cone scales, and the common name to the peninsula on which it grows extensively. Other common names are insignis pine and radiata pine. Radiata pine is a common name increasingly used worldwide; pino insigne is the Spanish equivalent.

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Physical Description

provided by USDA PLANTS text
Tree, Evergreen, Monoecious, Habit erect, Trees without or rarely having knees, Tree with bark rough or scaly, Young shoots 3-dimensional, Buds resinous, Leaves needle-like, Leaves alternate, Needle-like leaf margins finely serrulate (use magnification or slide your finger along the leaf), Leaf apex acute, Leaves > 5 cm long, Leaves < 10 cm long, Leaves yellow-green above, Leaves yellow-green below, Leaves not blue-green, Needle-like leaves triangular, Needle-like leaves twisted, Needle-like leaf habit erect, Needle-like leaves per fascicle mostly 3, Needle-like leaf sheath persistent, Twigs glabrous, Twigs viscid, Twigs not viscid, Twigs without peg-like projections or large fascicles after needles fall, Berry-like cones orange, Woody seed cones > 5 cm long, Seed cones bearing a scarlike umbo, Umbo with missing or very weak prickle, Bracts of seed cone included, Seeds brown, Seeds winged, Seeds unequally winged, Seed wings prominent, Seed wings equal to or broader than body.
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Pinus radiata

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Pinus radiata (syn. Pinus insignis), the Monterey pine,[3] insignis pine[4] or radiata pine, is a species of pine native to the Central Coast of California and Mexico (on Guadalupe Island and Cedros island). It is an evergreen conifer in the family Pinaceae.

P. radiata is a versatile, fast-growing, medium-density softwood, suitable for a wide range of uses and valued for rapid growth, as well as desirable lumber and pulp qualities.[5] Its silviculture reflects a century of research, observation and practice.[5] It is often considered a model for growers of other plantation species.[5]

Although P. radiata is extensively cultivated as a plantation timber in many temperate parts of the world,[6] it faces serious threats in its natural range,[7] due to the introduction of a fungal parasite, the pine pitch canker (Fusarium circinatum).

Description

Ovulate cone
Pollen cones, 2 cm scale bar

P. radiata is a coniferous evergreen tree growing to 15–30 m (50–100 ft) tall in the wild, but up to 60 m (200 ft) in cultivation in optimum conditions, with upward pointing branches and a rounded top. The leaves ("needles") are bright green, in clusters of three (two in var. binata), slender, 8–15 cm (3–6 in) long and with a blunt tip. The ovulate cones are 7–17 cm (3–6+12 in) long, brown, ovoid (egg-shaped), and usually set asymmetrically on a branch, attached at an oblique angle. The bark is fissured and dark grey to brown. When not cut short by disease or harvesting, it has a lifespan of 80 to 90 years.

The specific epiphet radiata refers to the cracks which radiate from the umbo of the cone scales.[8]

It is closely related to bishop pine and knobcone pine, hybridizing readily with both species; it is distinguished from the former by needles in threes (not pairs), and from both by the cones not having a sharp spine on the scales.

The modern tree is vastly different from the native tree of Monterey.[8] In plantations the tree is commonly planted at 4 square meter spacing on a wide variety of landscapes from flat to moderately steep hills.[8] Because of selective breeding and more recently the extensive use of growth factor seedlings, forests planted since the 1990s have very straight tall trunks without the problem of twin leaders.[8] The trees are pruned in three lifts so that the lower two-thirds of a mature tree is free of branches and hence of knots.[8]

Distribution and habitat

In the United States, it is native to three very limited areas located in Santa Cruz, Monterey, and San Luis Obispo Counties of California.

In Mexico, it is found on two islands in the Pacific Ocean, Guadalupe Island and Cedros Island. On Guadalupe Island, located 280 km (150 nmi) off of the mainland coast, the pines are found on the steep northern end of the island, at elevations of around 500 to 1,200 m (1,600 to 3,900 ft), where they follow the ridgetops and steep slopes. On Cedros Island, the pines are more abundant, being found in far greater numbers partly due to the lack of feral goats. They are found at lower elevations than on Guadalupe, at around 285 to 690 m (935 to 2,264 ft), on the windward ridges and canyons of the north and central parts of the island. In both cases, the pines seem to be heavily dependent on locations with a high frequency of fog.[9]

In Australia, New Zealand, and Spain it is the leading introduced tree[10] and in Argentina, Chile, Uruguay, Kenya, and South Africa it is a major plantation species. It is also an introduced tree on the world's most remote inhabited island, Tristan da Cunha.

Taxonomy

Subdivisions

Two varieties of this species have been recognized, each corresponding to the island they are endemic to in Baja California. Some authors lump these taxa and do not recognize infraspecies.[11]

On both islands it is the only pine species, and one of the few tree species. Compared to the mainland species, which are mostly three-needled, the insular varieties have their needles in bundles of two. Their cones are also smaller, and they show greater wind resistance in regards to wind-induced toppling.[9]

  • Pinus radiata var. binata (Engelm.) Lemmon — Commonly known as the Guadalupe Island pine. Endemic to Guadalupe Island.[11]
  • Pinus radiata var. cedrosensis (J.T. Howell) Silba — Commonly known as the Cedros Island pine. Endemic to Cedros Island.[11]

Ecology

Pinus radiata forest in Point Lobos, California

P. radiata is adapted to cope with stand-killing fire disturbance. Its cones are serotinous, i.e. they remain closed until opened by the heat of a forest fire; the abundant seeds are then discharged to regenerate on the burned forest floor. The cones may also burst open in hot weather.[12]

In its native range, P. radiata is associated with characteristic flora and fauna. It is the co-dominant canopy tree, together with Cupressus macrocarpa, which also naturally occurs only in coastal Monterey County.[13] Furthermore, one of the pine forests in Monterey, California, was the discovery site for Hickman's potentilla, an endangered species. Piperia yadonii, a rare species of orchid, is endemic to the same pine forest adjacent to Pebble Beach. In its native range, P. radiata is a principal host for the dwarf mistletoe Arceuthobium littorum.[14]

The habitat of the pines on Cedros Island contrasts greatly with the desert scrub on other parts of the island, forming zones of abrupt transition. The numerous groves form a mostly-monotypic forest of the species, with very few other plants besides seedlings emerging in the understory. In some areas, the edges of the forest form a zone that supports chaparral species, including Malosma laurina, Diplacus stellatus, and the endemic Eriogonum molle. With their large surfaces to condense fog, the pines create irrigation for themselves and their associates. Towards the far northern end of the island, a succulent community mostly consisting of Dudleya is found, and the endemic Dudleya pachyphytum can sometimes be found growing under the pines in the ecotone.[15]

A remnant P. radiata stand in Pacific Grove is a prime wintering habitat of the monarch butterfly.[16]

In South Africa, the tree is a threat to already scarce water resources.[17] The tree has remarkable roots. Monterey pine roots will reach downward as far as physically permitted by subterranean conditions. Roots have been discovered up to 12 meters (39 ft) long.[18] Efforts to remove large quantities of the non-native tree in areas of South Africa have resulted in significant increases in accessible water.[17]

Conservation status

Fungal disease

The three remaining wild stands of var. radiata (Monterey pine proper) are infected and under threat of extirpation from pine pitch canker caused by Fusarium circinatum, a fungal disease native to the southeast United States and found (in 1986) to have been introduced to California. When trees begin to die of the disease, they attract bark beetles which provide a pathway for infection of other trees. In some stands, 80–90% of trees are infected. If the disease is introduced in agroforestry areas dependent upon P. radiata, such as New Zealand, it could have catastrophic effects in those countries as well.[6]

Sphaeropsis blight (Diplodia pinea) infects P. radiata in California and causes serious damage to plantations of the species in New Zealand, Australia and South Africa,[19] especially after hail damage to growing tips.

Baja California

Pinus radiata var. binata

On Guadalupe Island, var. binata is critically endangered. Most of the population was destroyed as tens of thousands of feral goats ate binata seedlings and caused soil erosion from the mid-19th century until just a few years ago. The older trees gradually died off until by 2001–2002 the population stood at only one hundred. With a program to remove the goats essentially complete by 2005, hundreds of young Guadalupe pines have started to grow up in habitat fenced after 2001, the first significant new growth in about 150 years. Possible accidental introduction of pine pitch canker is considered the biggest threat at present to the survival of the Guadalupe Island pine population.[20] The University of California's Russell Reservation forestry research station hosts an orchard planted with 73 P. radiata seedlings from Guadalupe Island and plays an important role in conserving the binata variety.[21]

Cultivation

Australia

Monterey Pine trees in Kuitpo Forest near Adelaide in South Australia
Monterey Pine trees plantation in Prospect Hill, Pemulwuy near Sydney in New South Wales

P. radiata was introduced to Australia in the 1870s. It is "the dominant tree species in the Australian plantation estate"[22] – so much so that many Australians are concerned by the resulting loss of native wildlife habitat. The species is widely regarded as an environmental weed across southeastern and southwestern Australia[23] and the removal of individual plants beyond plantations is encouraged.[24] The Kuitpo Forest, 40 kilometres (25 miles) south-east of the Adelaide city centre, is a planted forest of Monterey Pine trees. 30 kilometres (19 miles) west of the Sydney city centre, there is a forest of introduced Monterey Pine trees in Prospect Hill, in the suburb of Pemulwuy.[25]

Chile

P. radiata has greatly replaced the Valdivian temperate rain forests, where vast plantations have been planted for timber, again displacing the native forests.[26] In 2001, this species produced 5,580,724 cubic meters of lumber, or 95% of Chile's total lumber production.[27] In 2021 1.3 million of Chile's 2.3 million ha of forest plantations were planted with Pinus radiata.[28]

New Zealand

The Monterey pine (always called "Radiata Pine" or Pinus radiata in New Zealand) was first introduced into New Zealand in 1859[29][30] and today 89% of the country's plantation forests are of this species.[31] This includes the Kaingaroa Forest (on the central plateau of the North Island), which is one of the largest planted forests in the world. Mass plantings became common from 1900 in the Rotorua area where prison labour was used. In some areas (particularly areas that were formerly grazed that have had stock removed) it is considered an invasive species (termed a wilding conifer or more commonly wilding pine) where it has escaped from plantations. It is the most extensively used wood in New Zealand.

Use of pine in construction did not become widespread until forced by wartime shortages. It had been used in Southland from about 1920,[32] but doubts were being expressed about it as late as 1945,[33] when at least one MP considered it only suitable for interior studding.[34] Experiments in pressure treatment with water-soluble preservatives were made from 1943.[35]

Spain

In the Iberian Peninsula since the nineteenth century they have been introduced mainly in the north area in order to take advantage of their wood for the manufacture of paper pulp and for shoring work in coal mines. It is found in low altitude areas of the Autonomous Communities of Galicia, Asturias, Cantabria, the Basque Country, and in the north of the Canary Islands.

P. radiata forests have a negative effect on local ecology. In its plantations there are usually no other tree species, while its shady undergrowth does not allow the existence of a rich stratum of scrub. 13% of the wood cut annually in Spain comes from this pine.[36]

United Kingdom

The cultivar P. radiata (Aurea Group) 'Aurea' has gained the Royal Horticultural Society's Award of Garden Merit.[37][38]

United States

P. radiata is widely used in private gardens and public landscapes in temperate California, and similar climates around the world. It is particularly commonly grown as a landscape tree in coastal areas of California outside of its native range, where the climate is virtually identical to its native range. It is fast-growing and adaptable to a broad range of soil types and climates, though it does not tolerate temperatures below about −15 °C (5 °F). Its fast growth makes it ideal for landscapes and forestry; in a good situation, P. radiata can reach its full height in 40 years or so. Though a combination of biotic and abiotic factors determines the natural distribution of P. radiata, humans have broadly expanded its distribution up and down the California coast, even reaching Oregon.[39]

Uses

Forty-five year old Pinus radiata bonsai at the National Arboretum in Canberra

As timber P. radiata is suitable for a wide variety of uses,[40] and has a resinous fragrance while being worked.[41] It holds screws and nails well and takes paint and stain without difficulty, and modern kiln dried timber is very easy to work.[42] It is about 1/3 heavier than dried western red cedar. It is brittle when bent, so does not have the same load-bearing features as Oregon pine (Douglas fir, Pseudotsuga).

P. radiata is used in house construction as weatherboards, posts, beams or plywood, in fencing, retaining walls, for concrete formers. It is also used to a limited extent in boat building where untreated ply is sometimes used, but must be encased in epoxy resin to exclude moisture.

The wood is normally kiln dried to 12% moisture in 6 m (19 ft 8 in) long, clear lengths. It is available treated with a range of chemical salts, or untreated. Chemical salt treatment is well proven and such timber is frequently used in the ground as posts and poles as part of structures such as retaining walls and pole houses. The name applied to this treatment is tanalized wood. H1 and H2 treatment is suited to indoor use. H3 is the standard house timber and this grade is used for fence palings. H4 and H5 are the standard for inground use. In New Zealand a 1995 change to no longer require boron treatment in house framing timber,[43] was a key factor in the leaky homes crisis,[44] but since 2003 a series of changes have now improved the regulations.[45]

Lower grade timber is converted to pulp to make newsprint.[46] Higher grade timber is used in house construction. P. radiata is used chipped to make particle board sheets, commonly used in flooring. Other sheet products are hardboard, softboard and ply. Most ply is structural and available in 7–22 mm (0.28–0.87 in) sizes. A small amount of higher grade ply is used to produce thinner (4 and 7 mm or 0.16 and 0.28 in) ply suitable for furniture, cabinet work and boat building. This is knot and crack free and glued with resorcinol waterproof glue. Since the 1990s finger jointed joinery-grade wood has become available in up to 6 m (19 ft 8 in) lengths in a wide range of profiles.

In 1958, New Zealand boat designer Des Townson started building 186 eleven-foot (3.35 m), cold-moulded Zephyr-class dinghies, using P. radiata. In 2011 these hand-built boats fetched very high prices and were generally in excellent condition.

The bark is used as a substrate for potting and re-potting orchids.

P. radiata is the most common species of Christmas tree in Australia and New Zealand.

In California, P. radiata is commonly planted to block wind or noise, or for ornamental reasons.[47]

References

  1. ^ Farjon, A. 2013. Pinus radiata. In: IUCN 2013. IUCN Red List of Threatened Species. Version 2013.1. www.iucnredlist.org. Downloaded on 13 July 2013.
  2. ^ "NatureServe Explorer 2.0".
  3. ^ BSBI List 2007 (xls). Botanical Society of Britain and Ireland. Archived from the original (xls) on 26 June 2015. Retrieved 17 October 2014.
  4. ^ Kershner, Bruce; et al. (2008). National Wildlife Federation Field Guide to Trees of North America. New York: Sterling. p. 84. ISBN 978-1-4027-3875-3.
  5. ^ a b c Mead, D (2013). Sustainable management of Pinus radiata. Rome: Food and Agriculture Organization of the United Nations. ISBN 978-92-5-107634-7.
  6. ^ a b Earle, Christopher J., ed. (2018). "Pinus radiata". The Gymnosperm Database.
  7. ^ "Status of Native Monterey Pine (Pinus radiata) Ecosystems" (PDF).
  8. ^ a b c d e Powell, Leslie (9 February 2017). The Genus Pinus: A Reference Guide for Pines. lulu.com. p. 112. ISBN 978-1365157172.
  9. ^ a b Rogers, Deborah L.; Jesús Vargas Hernández, J.; Matheson, A. Colin; Guerra Santos, Jesús J. (2005), Romero, Aldemaro; West, Sarah E. (eds.), "Conserving the Pines of Guadalupe and Cedros Islands, Mexico: An International Collaboration", Environmental Issues in Latin America and the Caribbean, Dordrecht: Springer Netherlands, pp. 31–54, doi:10.1007/1-4020-3774-0_2, ISBN 978-1-4020-3774-0, retrieved 21 July 2022
  10. ^ Scott, C. W. 1960. Pinus radiata. Food and Agriculture Organization of the United Nations, Forestry and Forest Products Study 14. Rome, Italy. 328 p. cited in McDonald & Laacke 1990 harvnb error: no target: CITEREFMcDonaldLaacke1990 (help).
  11. ^ a b c Rebman, J. P.; Gibson, J.; Rich, K. (2016). "Annotated checklist of the vascular plants of Baja California, Mexico" (PDF). San Diego Society of Natural History. 45: 131.
  12. ^ Little, Elbert L. Jr. (1980). The Audubon Society field guide to North American trees. New York: Alfred A. Knopf.
  13. ^ Hogan, C. Michael; Frankis, Michael P. (2009). "Monterey Cypress (Cupressus macrocarpa)". GlobalTwitcher.com. Archived from the original on 6 September 2017. Retrieved 14 January 2011.
  14. ^ Hawksworth, F.G.; Wiens, D. (1996). "Dwarf mistletoes: Biology, pathology and systematics". Agriculture Handbook 709. Washington, DC: U.S.D.A. Forest Service.
  15. ^ Oberbauer, Thomas A. (1987). "Floristic Analysis of Vegetation Communities on Isla de Cedros, Baja California, Mexico". Third California Islands Symposium: 115–131.
  16. ^ "Monarch Grove Sanctuary". Pacific Grove Museum of Natural History. Archived from the original on 17 July 2006. Retrieved 8 September 2006.
  17. ^ a b Balmford, Andrew (2012). Wild Hope. University of Chicago Press.
  18. ^ McDonald & Laacke 1990. sfn error: no target: CITEREFMcDonaldLaacke1990 (help)
  19. ^ "Diplodia Blight of Pines". Forest Insect & Disease Leaflet 161. Northeastern Area State and Private Forestry. Archived from the original on 16 October 2016. Retrieved 5 March 2015.
  20. ^ Junak, S; Keitt, B; Tershy, B; Croll, D; Sánchez, JA (13–14 November 2003). Recent conservation efforts and current status of the flora of Guadalupe Island, Baja California, Mexico. Taller sobre la Restauración y Conservación de Isla Guadalupe [Workshop on restoration and conservation of Guadalupe Island]. Instituto Nacional de Ecología. Archived from the original on 19 August 2007.
  21. ^ Rogers, Deborah L. "Status of Conservation of Monterey Pine" (PDF). Davis, CA: University of California. Archived from the original (PDF) on 10 June 2010. Retrieved 17 March 2012.
  22. ^ Lindenmayer, D.B.; Hobbs, R.J. (May 2007). "Fauna conservation in Australian plantation forests: a review" (PDF). Archived from the original (PDF) on 8 August 2017.
  23. ^ "Pinus radiata". Weeds of Australia Biosecurity Queensland Edition. Queensland Government.
  24. ^ "Weed Fact Sheets". Blue Mountains City Council. Archived from the original on 24 June 2015. Retrieved 1 August 2015.
  25. ^ "Radiata Pine". Weeds of the Blue Mountains. Blue Mountains City Council. Retrieved 8 April 2015.
  26. ^ Mary T. Kalin Arroyo & Adriana E. Hoffmann-J. "Temperate Rain Forest of Chile". Smithsonian Institution. Archived from the original on 18 April 2010.
  27. ^ "Douglas-fir Grown in Chile: Background" (PDF). Concepción, CHILE. October 2002.
  28. ^ Daniel, Soto Aguirre; Gysling Caselli, Janina; Kahler González, Carlos; Poblete Hernández, Pamela; Álvarez González, Verónica; Pardo Velásquez, Evaristo; Bañados, Juan Carlos; Baeza Rocha, Daniela (1 September 2021). "Statistical Yearbook 2021" (PDF). Statistical Bulletin. Instituto Forestal. 180.
  29. ^ "E: Pinus radiata". Downhill Walk to City – Trees of Note. Friends of the Wellington Botanic Garden Inc. Archived from the original on 26 May 2010. Retrieved 7 September 2010. The Acland family at Mount Peel Station had made the first NZ introduction of British seedlings in 1859...
  30. ^ "Radiata pine". Te Ara.
  31. ^ "Situation and outlook for New Zealand agriculture and forestry" (PDF). NZ Ministry of Agriculture and Forestry. 2007. Archived from the original (PDF) on 22 May 2010. Retrieved 19 October 2010.
  32. ^ "PINUS RADIATA – UTILISATION AS bUILDING TIMBER (Bay of Plenty Beacon, 1945-12-18)". Papers Past. National Library of New Zealand. Retrieved 5 May 2017.
  33. ^ "FOR HOUSE BUILDING – PINUS RADIATA CONDEMNED (Auckland Star, 1945-12-15)". Papers Past. National Library of New Zealand. Retrieved 5 May 2017.
  34. ^ "PARLIAMENT IN SESSION – DAY'S DEBATE (New Zealand Herald, 1945-07-07)". Papers Past. National Library of New Zealand. Retrieved 5 May 2017.
  35. ^ "DEPARTMENT OF SCIENTIFIC AND INDUSTRIAL RESEARCH (NINETEENTH ANNUAL REPORT OF THE) (Appendix to the Journals of the House of Representatives, 1 January 1945)". Papers Past. National Library of New Zealand. Retrieved 5 May 2017.
  36. ^ Los pinares de pino radiata Los pinares de pino radiata Ministerio de Medio Ambiente. Gobierno de España.
  37. ^ "RHS Plantfinder – Pinus radiata (Aurea Group) 'Aurea'". Retrieved 30 April 2018.
  38. ^ "AGM Plants – Ornamental" (PDF). Royal Horticultural Society. July 2017. p. 71. Retrieved 25 April 2018.
  39. ^ George, Zach St. "The Tree That's Rare, Endangered and Common – Bay Nature Magazine". Bay Nature. Retrieved 14 November 2020.
  40. ^ "Radiata pine" Archived 11 April 2011 at the Wayback Machine, Primary Industries and Fisheries, QLD
  41. ^ "Radiata Pine – The Wood Database – Lumber Identification (Softwood)". wood-database.com.
  42. ^ "Radiata pine", nzwood.co.nz
  43. ^ "Background note: Information briefing for members of Parliament:Leaky buildings" (PDF). NZ Parliamentary Library. 6 November 2002. Archived from the original (PDF) on 2 November 2012.
  44. ^ "Leaky homes will cost $11.3b to fix – report". The New Zealand Herald. 22 December 2009. Retrieved 26 February 2012.
  45. ^ "*ARCHIVE* – BIA Update No. 20 – Changes to Acceptable Solution B2/AS1 – Timber Durability 23 Dec 2003". dbh.govt.nz. 9 March 2004. Archived from the original on 13 November 2007.
  46. ^ "Norske Skog Tasman".
  47. ^ "Pinus radiata D". srs.fs.usda.gov. Retrieved 24 November 2020.
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Pinus radiata: Brief Summary

provided by wikipedia EN

Pinus radiata (syn. Pinus insignis), the Monterey pine, insignis pine or radiata pine, is a species of pine native to the Central Coast of California and Mexico (on Guadalupe Island and Cedros island). It is an evergreen conifer in the family Pinaceae.

P. radiata is a versatile, fast-growing, medium-density softwood, suitable for a wide range of uses and valued for rapid growth, as well as desirable lumber and pulp qualities. Its silviculture reflects a century of research, observation and practice. It is often considered a model for growers of other plantation species.

Although P. radiata is extensively cultivated as a plantation timber in many temperate parts of the world, it faces serious threats in its natural range, due to the introduction of a fungal parasite, the pine pitch canker (Fusarium circinatum).

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