|
Wildlife, Animals, and Plants
|
|
Introductory
SPECIES: Sequoiadendron giganteum | Giant Sequoia
ABBREVIATION :
SEQGIG
SYNONYMS :
Sequoia gigantea (Lindl.) Buchholz
SCS PLANT CODE :
SEGI2
COMMON NAMES :
giant sequoia
bigtree
TAXONOMY :
The currently accepted scientific name for giant sequoia is
Sequoiadendron giganteum (Lindl.) Buchholz [26,28]. There are no
recognized subspecies, varieties, or forms.
LIFE FORM :
Tree
FEDERAL LEGAL STATUS :
See OTHER STATUS
OTHER STATUS :
NO-ENTRY
COMPILED BY AND DATE :
R. J. Habeck, May 1992
LAST REVISED BY AND DATE :
NO-ENTRY
AUTHORSHIP AND CITATION :
Habeck, R. J. 1992. Sequoiadendron giganteum. In: Remainder of Citation
DISTRIBUTION AND OCCURRENCE
SPECIES: Sequoiadendron giganteum | Giant Sequoia
GENERAL DISTRIBUTION :
The natural distribution of giant sequoia is restricted to about 75
groves, comprising a total area of only 35,607 acres (14,416 ha) along a
limited area of the western Sierra Nevada, California. The northern
two-thirds of its range, from the American River in Placer County
southward to the Kings River has only eight disjunct groves. The
remaining groves are concentrated between the Kings River and the Deer
Creek Grove in southern Tulare County [10,28]. Groves range in size
from approximately 2,470 acres (1,000 ha) with 20,000 giant sequioas to
small groves with only six living trees [24].
ECOSYSTEMS :
FRES21 Ponderosa pine
FRES23 Fir - spruce
FRES28 Western hardwoods
STATES :
CA HI
ADMINISTRATIVE UNITS :
KICA SEQU YOSE
BLM PHYSIOGRAPHIC REGIONS :
4 Sierra Mountains
KUCHLER PLANT ASSOCIATIONS :
K005 Mixed conifer forest
SAF COVER TYPES :
243 Sierra Nevada mixed conifer
SRM (RANGELAND) COVER TYPES :
NO-ENTRY
HABITAT TYPES AND PLANT COMMUNITIES :
Giant sequoia principally occurs in scattered groves. Nowhere does it
grow in pure stands, although in a few small areas stands do approach a
pure condition [28]. Although the giant sequoia groves of the central
and southern Sierra Nevada represent only a specific mesic segregate of
typical white fir (Abies concolor) forest communities, these groves are
often given special community recognition. Only giant sequoia is
restricted to the groves [24].
Typically, giant sequoia is found in a mixed conifer type dominated by
California white fir (A. concolor var. lowiana). Characteristic
associates include sugar pine (Pinus lambertiana), Jeffrey pine (P.
jeffreyi), ponderosa pine (P. ponderosa), Douglas-fir (Pseudotsuga
menziesii), incense-cedar (Calocedrus decurrens), and California black
oak (Quercus kelloggii). Shrub types include bush chinkapin
(Castanopsis sempervirens) and mountain whitethorn (Ceanothus
cordulatus) [10,14,28].
Giant sequoia as a dominant species in the following typings:
Terrestrial natural communitites of California [29]
Montane and subalpine vegetation of the Sierra Nevada and Cascade Ranges [24]
VALUE AND USE
SPECIES: Sequoiadendron giganteum | Giant Sequoia
WOOD PRODUCTS VALUE :
Giant sequoia was cut commercially from the 1850's up to the mid-1950's.
Young giant sequoia has favorable wood properties. It is
decay-resistant and used as dimensional lumber, veneer, and plywood
[21]. Old growth has low tensile strength and brittleness, making it
unsuitable for most structural purposes. The most histroically popular
items milled from giant sequoia were fenceposts, grape stakes, shingles,
novelties, patio furniture, and pencils [10].
IMPORTANCE TO LIVESTOCK AND WILDLIFE :
Only a limited number of wildlife species utilize giant sequoia for food
and shelter.
Birds: Over 30 bird species have been identified in giant sequoia
groves. A variety of foliage- and air-feeding birds occupy the upper
canopy, while sapsuckers feed through the thin bark. Cavity-nesters
that use giant sequoia for nesting include white-headed woodpeckers and
flickers, and an occasional perching bird such as a nuthutch.
Mammals: Common mammal associates include the deer mouse, chipmunk,
shrew, gray squirrel, golden-mantled ground squirrel, mule deer, coyote,
black bear, and various reptiles. Reports of chipmunks using giant
sequoia sawdust for cleansing baths have been noted. The chickaree is
especially noted for its relationship to giant sequoia. Chickarees make
the soft flesh of green giant sequoia cone scales a major food item. An
individual chickaree may cut and eat as many as 3,000 to 3,500 cones per
year [10,12].
PALATABILITY :
Deer browse on 4- and 5-year-old giant sequoia; however, it is generally
considered low in palatability [10].
NUTRITIONAL VALUE :
The mean caloric value of giant sequoia seeds is 4,738 calories per gram
dry weight. The outer portions of the cones provide 4,690 calories per
gram dry weight [12].
COVER VALUE :
Wildlife primarily use giant sequoia for cover. Early in giant sequoia
development, large mammals use dense stands as hiding and thermal cover.
Mature trees are used to a limited extent by arboreal species such as
birds, squirrels, and other small mammals [10].
VALUE FOR REHABILITATION OF DISTURBED SITES :
NO-ENTRY
OTHER USES AND VALUES :
Giant sequoia is planted as an ornamental inside and outside of its
native range. It is also used for Christmas trees [28].
MANAGEMENT CONSIDERATIONS :
Insects: Insects do not seriously harm giant sequoias older than about
2 years. Carpenter ants (Campanotus laevigatus) do not directly harm
the trees, although they do create pathways for fungi [28]. A
wood-boring beetle (Trachykele opulenta) may kill trees damaged by road
cuts or the undercutting of stream banks. The larvae of this beetle may
girdle a giant sequoia by feeding on the inner bark. The cerambycid
beetle (Phymatodes nitidus) lays its larvae in green giant sequoia
cones. Other cone larvae predators are the gelechiid moth (Gelechia
spp.) and lygaeid bug (Ischnorrhynchus resedae). In all, 151 species of
insects and 37 arachnids are known to be associated with the giant
sequoia in that they use it to complete some part of their life cycle
[12,19,28].
Disease: At least nine fungi have been found associated with decayed
giant sequoia wood. The most prevalent fungi are Heterobasidion
annosum, Armillaria mellea, Poria incrassata, and P. albipellucida.
Diseases generally do not kill trees past the seedling stage directly,
but rather by contributing to root or stem failure. No other types of
disease, including seedling disease, are known to be problems to giant
sequoia [12,19,28].
Air-pollution creating acidic mists significantly reduce root growth of
giant sequoia [25]. The development of facilities for human use, such
as paved roads and buildings, can damage giant sequoia roots and hence
slow growth [27].
BOTANICAL AND ECOLOGICAL CHARACTERISTICS
SPECIES: Sequoiadendron giganteum | Giant Sequoia
GENERAL BOTANICAL CHARACTERISTICS :
Giant sequoias grow to an average height of 250 to 275 feet (76-84 m)
and 15 to 20 feet (5-7 m) d.b.h. Record trees have been reported to be
310 feet (95 m) in height and 35 feet (11 m) d.b.h. The leaves are
awl-shaped, sessile, and persistent. Seed cones are 2 to 3 inches (5-8
cm) long, serotinous, persistent, and may remain green up to 20 years.
Bark is fibrous, furrowed, and may be 2 feet (0.6 m) thick at the base
of the columnar trunk [6,10]. The oldest known giant sequoia based on
ring count is 3,200 years old [10].
RAUNKIAER LIFE FORM :
Phanerophyte
REGENERATION PROCESSES :
Giant sequoia regenerates primarily by seed, although occasionally it
may reproduce naturally by vegetative methods. Giant sequoias up to
about 20 years of age may produce stump sprouts subsequent to injury.
Giant sequoia of all ages may sprout from the bole when old branches are
lost to fire or breakage. Cuttings from juvenile donors root quickly
and in high percentages (up to 94 percent) [10].
Flowering and fruiting: Giant sequoia is monecious; male and female
cone buds form during late summer. Pollination takes place between the
middle of April and May. Fertilization usually occurs in August when
the cones are nearly full-sized. Embryos develop rapidly during the
next summer and reach maturity at the end of the second growing season.
Seed production and dissemination: Young trees start to bear cones at
the age of 20 years. Cones may remain attached to the tree for 8 to 12
years and much of the seed will be retained. During the late summer,
however, some seed is shed when the cone scales shrink. Most seeds are
liberated when the cone drys out and becomes detached. Each cone yields
an average of 230 seeds. The average number of cleaned seeds per pound
is approximately 81,000 (200,070/kg). Stored giant sequoia seed remains
moderately viable for many years [5,10,28]. At any given time, a large
tree may be expected to have approximately 11,000 cones. The upper part
of the crown of any mature giant sequoia invariably produces a greater
abundance of cones than its lower portions.
A mature giant sequoia has been estimated to disperse from 300,000 to
400,000 seeds per year. Seed dispersal results from seed falling from
the tree-top, insect and rodent activity, or by cones falling to the
ground. The winged seeds may be carried up to 600 feet (183 m) from the
parent tree.
Seedling development: Giant sequoia seeds germinate best when totally
buried in disturbed mineral soil. April, May, September, and October
temperatures are best for early development. Soil moisture conditions
and seedling survival are generally better in spring than during any
other season. Light conditions are generally best for growing at
one-half full sunlight. Upon germination, the seedling stands 3/4 to 1
inch (1.9-2.5 cm) high, usually with four cotyledons. By autumn,
seedlings have up to six branches and are 3 to 4 inches (8-10 cm) tall.
After the second year, the seedling attains a height of 8 to 12 inches
(20-30 cm) with a taproot penetrating to a depth of 10 to 15 inches
(25-38 cm) [28].
Growth and yield: Giant sequoia is the worlds largest tree in terms of
total volume. Beyond the seedling stage, giant sequoia unhindered by an
overstory continues to grow at the same rate as its competitors. Yields
of second growth stands dominated by giant sequoia were found to equal
or slightly exceed those of second-growth mixed-conifer stands on the
same site. Lower branches die fairly readily from shading, but trees
less than 100 years old retain most of their dead branches. Boles of
mature trees generally are free of branches to a height of 98 to 148
feet (30-40 m) [28].
SITE CHARACTERISTICS :
Low temperatures seem to be the limiting factor for giant sequoia at the
upper elevational limits of its range, as well as in areas with severe
winters where the species has been introduced. Distribution of giant
sequoia at lower elevations appears to be restricted to sites with
available soil moisture throughout the summer drought period [24,28].
Climate: Giant sequoia is found in a humid climate characterized by dry
summers. Mean annual precipitation varies from 35 to 55 inches (88-138
cm). Most precipitation comes in the form of snow between October and
April. Mean annual snowfall ranges from 144 to 197 inches (360-493 cm),
and snow depths of 6.6 feet (2 m) or greater are common. Mean daily
maximum temperatures for July are typically 75 to 84 degrees Fahrenheit
(24-29 deg C). Mean minimum temperatures for January vary from 34 to 21
degrees Fahrenheit (1 to -6 deg C) [28].
Soils and topography: Most giant sequoia groves are on granitic-based
residual and alluvial soils. Some groves are on glacial outwash from
granite. Other common parent materials include schistose, dioritic and
andesitic rocks. Giant sequoia grows best in deep, well-drained sandy
loams. It occurs with higher frequency on mesic sites, such as drainage
bottoms and meadow edges. Soil pH ranges from 5.5 to 7.5, with an
average of about 6.5. Long-term site occupancy develops soil of high
fertility, good base status, and low bulk density. Except for its
moisture content, soil typically plays only a minor role in influencing
the distribution of the species [28].
Elevation: Elevation of the giant sequoia groves generally range from
4,590 to 6,560 feet (1,400-2,000 m) in the north, and 5,580 to 7,050
(1,700-2,150 m) to the south. The lowest natural occurrence of the
species is 2,720 feet (830 m) and the highest is 8,860 feet (2,700 m).
Giant sequoia generally appears on southern slopes in its northern
distribution and on more northerly slopes in the south [28].
SUCCESSIONAL STATUS :
Giant sequoia has adapted to keep its crown higher than that of its
associates. On disturbed sites, giant sequoia is a strong competitor,
although never totally dominating a stand [10]. Current data does not
indicate that any enlargement of giant sequoia groves is taking place.
Mature giant sequoia mark the outer boundaries, which have remained
stable over a period of 500 to 1,000+ years. High levels of
reproduction are not necessary to maintain the present population
levels. Few groves, however, have sufficient young trees to maintain
the present density of mature giant sequoias for the future. The
majority of giant sequoias are currently undergoing a gradual decline in
density since the European settlement days [24].
SEASONAL DEVELOPMENT :
Giant sequoia flowers from April to May; cone ripening and seed
dispersal occurs in the spring and summer months. Seeds dropped just
before the first snow or just as the snow melts may have the best chance
of germinating and becoming successfully established. Growth of giant
sequoia generally begins in the early spring to late fall [28].
FIRE ECOLOGY
SPECIES: Sequoiadendron giganteum | Giant Sequoia
FIRE ECOLOGY OR ADAPTATIONS :
Fire is the most serious damaging agent to young giant sequoia.
Seedlings and saplings are highly susceptible to mortality or serious
injury by fire. Giant sequoia exhibits the following adaptations to
fire: rapid growth, fire resistant bark, elevated canopies and
self-pruned lower branches, latent buds, and serotinous cones [10,12].
Mature giant sequoia are more resistant to fire damage and few are
killed by fire alone [28].
Giant sequoia groves represent a fire climax community whose stability
is maintained by frequent fires. In the absence of regular ground
fires, litter accumulates on the forest floor and limits germination and
establishment of seedlings [24]. Giant sequoia in Whitaker's Forest,
California, produced 9,089 pounds per acre (10,181 kg per ha) of ground
litter [3]. If these conditions are maintained in the future, the
groves will become a long-standing seral community trending toward a
mature white fir forest without giant sequoia [24].
POSTFIRE REGENERATION STRATEGY :
crown-stored residual colonizer; long-viability seed in on-site cones
off-site colonizer; seed carried by wind; postfire years 1 and 2
off-site colonizer; seed carried by animals or water; postfire yr 1&2
FIRE EFFECTS
SPECIES: Sequoiadendron giganteum | Giant Sequoia
IMMEDIATE FIRE EFFECT ON PLANT :
In Sequoia and Kings Canyon National Parks, a moderate-severity
prescribed fire contributed little to the mortality of giant sequoia
that were larger than 1 foot (0.30 m) d.b.h. Additionally, there is no
evidence that previous fire scarring had any relationship to tree
mortality [5]. Low- to moderate-severity fires scorch the bark of giant
sequoia and usually cause scarring. High-severity fires may reach the
crown and consume part or all of the canopy cover [2]. A direct
relationship exists between the size of the basal fire scar in mature
giant sequoias and the the likelihood of damage to the top or foliage of
the trees [23]. Reduction of supporting wood from scarring predisposes
the tree to falling, and provides an opening for fungi responsible for
root disease and heart rot [28].
DISCUSSION AND QUALIFICATION OF FIRE EFFECT :
Despite the general belief that giant sequoia wood is not especially
flammable, it burns hotly when splintered and dry [10].
PLANT RESPONSE TO FIRE :
High-severity fires will generally kill pole-size and younger trees.
Immediately following the passage of fire, seeds will drop as a reaction
to hot convectional air movement through the canopy. Seeds will
germinate on the favorable mineral seedbeds created by the fire [5].
Postfire seedling establishment: When high-severity fires burn in dense
stands of mature giant sequoias, as many as 40,485 seedlings per acre
(100,000/ha) may develop following heat-induced seedfall [11]. After a
prescribed burn in Sequoia and Kings Canyon National Parks, a
high-severity burn resulted in 40,000 seedlings per acre (98,800/ha) the
first year after burning. A lower-severity burn resulted in 13,000
seedlings per acre (32,110/ha). Not a single giant sequoia seedling was
found on the unburned control plot in this study [5].
DISCUSSION AND QUALIFICATION OF PLANT RESPONSE :
NO-ENTRY
FIRE MANAGEMENT CONSIDERATIONS :
Research on the importance of periodic fire in maintaining natural giant
sequoia forests has justified the need to restore a natural fire regime.
The principal goal of fire management in giant sequoia groves in
Sequoia, Kings Canyon, and Yosemite National Parks is to restore or
maintain the natural fire regime to the maximum extent possible.
Prescribed burns are now conducted by igniting fires in a spot pattern
and allowing nature to produce a mosaic of effects [20].
The long-standing fire suppression policy of federal and state land
agencies has created at least two major problems for the giant sequoia:
(1) the continuing reproduction of the species has been seriously
hampered and (2) the build-up of dead fuels and the growth of other
young trees in the understory pose threats of destructive forest fires
in the crowns of existing groves. In 1969, the National Park Service
began a program or prescribed burning in Kings Canyon National Park.
Prescribed burning has produced relatively few deleterious side effects
on giant sequoia groves [27].
Prescribed burning is currently an active management strategy in giant
sequoia groves. Fire prepares seedbeds, recycles nutrients, maintains
successional diveristy, decreases the number of trees susceptible to
attack by insects and disease, reduces fire hazards, and favors wildlife
[5,10,27]. A prescribed burn in Kings Canyon National Park resulted in
an increase in flycatcher and robin numbers [4,13]. A number of changes
in bird and mammal populations are forecasted if fire is reintroduced on
a large scale. High-severity fire will increase the number of
trunk-feeding birds preying on the increased amount of insects [12].
Prior to protection under Park status in 1864, the Mariposa Grove and
Yosemite National Park sustained fires every 20 to 25 years [9]. Other
research found that in presettlement times, any given site in the middle
elevations of the Sierra was burned over every 5 to 10 years [18,27].
FIRE CASE STUDIES
SPECIES: Sequoiadendron giganteum | Giant Sequoia
CASE NAME :
Impact of prescribed burning on a sequoia-mixed conifer forest
REFERENCE :
Kilgore, B. M. 1973 [30]
SEASON/SEVERITY CLASSIFICATION :
Fall burn / low- to moderate-severity
STUDY LOCATION :
The study site was located on the ridge of Redwood Mountain which runs
north and south within the 3,100 acre Redwood Mountain Grove of giant
sequoias in Kings Canyon National Park, Three Rivers, California.
PREFIRE VEGETATIVE COMMUNITY :
Giant sequoia, white fir, and sugar pine dominate the forest, with
incense-cedar, Pacific ponderosa pine, and California black oak well
represented except in the extreme southern plots. Shrubs and herbs are
present, but rare, and grasses are almost absent. Major shrub species
include Sierra mountain misery (Chamaebatia foliolosa) and Sierra
gooseberry (Ribes roezlii). Graminoids include Carex spp.
TARGET SPECIES PHENOLOGICAL STATE :
The target phenological states were not recorded.
SITE DESCRIPTION :
The elevation along the ridge ranges from 6,400 feet (1,950 m) at the
saddle to nearly 7,000 feet (2,134 m). Hygrothermograph records show a
yearly low of 17 degrees Fahrenheit (-8.4 deg C) and a high of 82
degrees Fahrenheit (28 deg C). Temperatures in November just before the
burn ranged from 32 to 58 degrees Fahrenheit (0-15 deg C). Relative
humidity fluctuated between 30 and 80 percent. Winds in and near the
study plots were moderate when present, varying from 0 to 5 mph (0.3
kmh). Average slope was 35 percent. Large portions of this study area
were found on soils derived from metamorphic schists.
Burn day conditions were as follows:
Temperature: 59 deg F (15 deg C)
Humidity: 20 percent
10-hour fuel sticks: 10 grams
Wind speed: 0 mph
FIRE DESCRIPTION :
Twelve 60- by 100-foot (18 x 30 m) study plots were laid out about 600
feet (183 m) east of the ridge of Redwood Mountains at an elevation of
6,300 feet (1,920 m). Two additional plots were established just below
the saddle parking area as demonstration plots. These were selected as
being represenative of the range of vegetative and fuel conditions on
this east-facing slope of the mountain. Seven of the 12 plots and 1
demonstration plot were burned, while the remaining plots were retained
as controls. For each plot, the following information was measured
before and after ignition:
1. Species, diameter, height class > 6 inches dbh (15 cm) or 4.5 feet
(1.4 m) tall.
2. Number of white fir and sugar pine saplings per acre in four height
classes.
3. Extent and approximate height of white fir sapling thickets.
4. Coverage and frequency values.
5. Litter and duff weights.
6. Length and diameter of down trees.
7. Chemical light meter indices for light reaching the forest floor.
8. Vegetation appearance recorded by black and white/color photographs
from 102 permanent photo points.
After all pre-burn measurements were made, a 2-foot (0.6 m) wide
fire-line was built along the 2 sides and the bottom of the proposed
5-acre (2 ha) burn area. The burning indices for the burn day were as
follows:
Forecast Actual Prescription (range)
-------- ------ --------------------
Fine Fuel Moisture 6 5 7-10
Spread Index 8 8 5-12
Intensity Index 59 56 37-49
Timber Burning Index 5 5 3-5
Ignition Index 45 55 15-49
All test plots were ignited at 0900 by drip torch along the upper
boundary of the burn area. A strip-head fire method of ignition was
used and it burned briskly from 0900 to 1200.
FIRE EFFECTS ON TARGET SPECIES :
Ninty-four percent of the 210 2- by 3-foot (0.6 x 0.9 m) sample plots
showed evidence of fire impact. Eighty percent burned almost
completely, while 14 percent burned partially or lightly. Only 6
percent of the sample plots remained unburned. Both before and after
the burn, about 55 percent of the trees more than 12 inches dbh were
white fir, while 29 percent were sequoia and only 8 percent were sugar
pine. More than 84 percent of the trees in the 6 to 12 inch d.b.h class
were white fir, with the remainder being sugar pine. About 38 percent
of this class was killed during the burn, but the proportion of white
fir to sugar pine remained nearly the same.
Essentially no tree seedlings of any species were found during the first
year following this November 1970 burn. This is in sharp contrast with
the nearly 22,000 sequoia seedlings per acre found on a previous, more
intense August-September 1969 burn on the ridge itself.
FIRE MANAGEMENT IMPLICATIONS :
This study investigated methods by which the impacts of prescribed fire
on certain biotic and abiotic elements of the sequoia-mixed conifer
forest ecosystem could be measured. Giant sequoia was present as a
co-dominant species with an estimated 11.4 trees per acre (28.2/ha). A
comparison of results was detailed from previous high-severity 1969 burn
to the lower-severity 1970 burn reported here. In summary, a high-severity
burn followed by another moderate-severity burn 7 to 10 years later is
an option for obtaining management objectives on a mixed sequoia stand;
or, alternatively, implement two low-severity burns in closer sequence
in order to gradually kill young seedlings and cleanup heavy fuels.
Both strategies would allow for more natural regeneration of seral species,
while reducing the potential threat of hazardous wildfires.
REFERENCES
SPECIES: Sequoiadendron giganteum | Giant Sequoia
REFERENCES :
1. Bernard, Stephen R.; Brown, Kenneth F. 1977. Distribution of mammals,
reptiles, and amphibians by BLM physiographic regions and A.W. Kuchler's
associations for the eleven western states. Tech. Note 301. Denver, CO:
U.S. Department of the Interior, Bureau of Land Management. 169 p.
[434]
2. Biswell, H. H. 1961. The big trees and fire. National Parks Magazine.
April: 1-4. [8786]
3. Biswell, H. H.; Gibbens, R. P.; Buchanan, H. 1966. Litter production by
bigtrees and associated species. California Agriculture. 20(9): 5-7.
[12692]
4. Bock, Carl E.; Lynch, James F. 1970. Breeding bird populations of burned
and unburned conifer forest in the Sierra Nevada. Condor. 72: 182-189.
[5113]
5. Boe, Kenneth N. 1974. Sequoiadendron giganteum (Lindl.) Buchholz Giant
sequoia. In: Schopmeyer, C. S., ed. Seeds of woody plants in the United
States. Agriculture Handbook No. 450. Washington: U. S. Department of
Agriculture, Forest Service: 767-768. [7751]
6. Brockman, C. Frank. 1979. Trees of North America. New York: Golden
Press. 280 p. [16867]
7. Eyre, F. H., ed. 1980. Forest cover types of the United States and
Canada. Washington, DC: Society of American Foresters. 148 p. [905]
8. Garrison, George A.; Bjugstad, Ardell J.; Duncan, Don A.; [and others].
1977. Vegetation and environmental features of forest and range
ecosystems. Agric. Handb. 475. Washington, DC: U.S. Department of
Agriculture, Forest Service. 68 p. [998]
9. Hartesveldt, R. J.; Harvey, H. T. 1968. The fire ecology of Sequoia
regeneration. In: Proceedings, Tall Timbers fire ecology conference;
1967 November 9-10; Hoberg. No. 7. Tallahassee, FL: Tall Timbers
Research Station: 65-77. [6384]
10. Hartesveldt, Richard J.; Harvey, H. Thomas; Shellhammer, Howard S.;
Stecker, Ronald E. 1975. The sequoia of the Sierra Nevada. Washington,
DC: U.S. Department of the Interior, National Park Service. 180 p.
[4233]
11. Harvey, H. Thomas; Shellhammer, Howard S. 1991. Survivorship and growth
of giant sequoia (Sequoiadendron giganteum (lindl.)buchh.) seedlings
after fire. Madrona. 38(1): 14-20. [14879]
12. Harvey, H. Thomas; Shellhammer, Howard S.; Stecker, Ronald E. 1980.
Giant sequoia ecology: Fire and reproduction. Scientific Monograph
Series No 12. Washington, DC: U.S. Department of the Interior, National
Park Service. 182 p. [6587]
13. Kilgore, Bruce M. 1971. Response of breeding bird populations to habitat
changes in a giant sequoia forest. American Midland Naturalist. 85(1):
135-152. [7281]
14. Kilgore, Bruce M. 1972. Fire's role in a Sequoia forest. Naturalist.
23(1): 26-37. [8783]
15. Kuchler, A. W. 1964. Manual to accompany the map of potential vegetation
of the conterminous United States. Special Publication No. 36. New York:
American Geographical Society. 77 p. [1384]
16. Lambert, Sherman; Stohlgren, Thomas J. 1988. Giant sequoia mortality in
burned and unburned stands. Journal of Forestry. 86(2): 44-46. [7221]
17. Lyon, L. Jack; Stickney, Peter F. 1976. Early vegetal succession
following large northern Rocky Mountain wildfires. In: Proceedings, Tall
Timbers fire ecology conference and Intermountain Fire Research Council
fire and land management symposium; 1974 October 8-10; Missoula, MT. No.
14. Tallahassee, FL: Tall Timbers Research Station: 355-373. [1496]
18. Martin, Robert E. 1982. Fire history and its role in succession. In:
Means, Joseph E., ed. Forest succession and stand development research
in the Northwest: Proceedings of a symposium; 1981 March 26; Corvallis,
OR. Corvallis, OR: Oregon State University, Forest Research Laboratory:
92-99. [9830]
19. Parmeter, John R., Jr. 1986. Diseases and insects of giant sequoia. In:
Weatherspoon, C. Phillip; Iwamoto, Y. Robert; Piirto, Douglas D.,
technical coordinators. Proceedings of the workshop on management of
giant sequoia; 1985 May 24-25; Reedley, CA. Gen. Tech. Rep. PSW-95.
Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific
Southwest Forest and Range Experiment Station: 11-13. [9803]
20. Parsons, David J.; Nichols, H. Thomas. 1986. Management of giant sequoia
in the national parks of the Sierra Nevada, California. In:
Weatherspoon, C. Phillip; Iwamoto, Y. Robert; Piirto, Douglas D.,
technical coordinators. Proceedings of the workshop on management of
giant sequoia; 1985 May 24-25; Reedley, CA. Gen. Tech. Rep. PSW-95.
Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific
Southwest Forest and Range Experiment Station: 26-29. [9807]
21. Piirto, Douglas D. 1986. Wood of giant sequoia: properties and unique
characteristics. In: Weatherspoon, C. Phillip; Iwamoto, Y. Robert;
Piirto, Douglas D., technical coordinators. Proceedings of the workshop
on management of giant sequoia; 1985 May 24-25; Reedley, CA. Gen. Tech.
Rep. PSW-95. Berkeley, CA: U.S. Department of Agriculture, Forest
Service, Pacific Southwest Forest and Range Experiment Station: 19-23.
[9806]
22. Raunkiaer, C. 1934. The life forms of plants and statistical plant
geography. Oxford: Clarendon Press. 632 p. [2843]
23. Rundel, Philip W. 1973. The relationship between basal fire scars and
crown damage in giant sequoia. Ecology. 54(1): 210-213. [6639]
24. Rundel, Philip W.; Parsons, David J.; Gordon, Donald T. 1977. Montane
and subalpine vegetation of the Sierra Nevada and Cascade Ranges. In:
Barbour, Michael G.; Major, Jack, eds. Terrestrial vegetation of
California. New York: John Wiley & Sons: 559-599. [4235]
25. Temple, Patrick J. 1988. Injury and growth of Jeffrey pine and giant
sequoia in response to ozone and acidic mist. Environmental and
Experimental Botany. 28(4): 323-333. [13016]
26. U.S. Department of Agriculture, Soil Conservation Service. 1982.
National list of scientific plant names. Vol. 1. List of plant names.
SCS-TP-159. Washington, DC. 416 p. [11573]
27. Vale, Thomas R. 1975. Ecology and environmental issues of the Sierra
Redwood (Sequoiadendron giganteum), now restricted to California.
Environmental Conservation. 2(3): 179-188. [8776]
28. Weatherspoon, C. Philip. 1990. Sequoiadendron giganteum (Lindl.)
Buchholz. In: Burns, Russell M.; Honkala, Barbara H., technical
coordinators. Silvics of North America. Volume 1. Conifers. Agric.
Handb. 654. Washington, DC: U.S. Department of Agriculture, Forest
Service: 552-562. [13415]
29. Holland, Robert F. 1986. Preliminary descriptions of the terrestrial
natural communities of California. Sacramento, CA: California Department
of Fish and Game. 156 p. [12756]
30. Kilgore, B. M. 1973 [6270]
Index
Related categories for Species: Sequoiadendron giganteum
| Giant Sequoia
|
 |