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Introductory

SPECIES: Quercus wislizenii | Interior Live Oak
ABBREVIATION : QUEWIS SYNONYMS : Quercus parvula Quercus shrevei SCS PLANT CODE : QUWI2 COMMON NAMES : interior live oak dwarf interior live oak scrub interior live oak highland live oak Sierra live oak TAXONOMY : The currently accepted scientific name of interior live oak is Quercus wislizenii A. DC [5]. Interior live oak is a member of the black or red oak subgenus Erythrobalanus [2,7]. It readily hybridizes with other sympatric oaks including California black oak (Q. kellogii) and California live oak (Q. agrifolia) [2,3,4,10]. The oracle oak (Q. x morehus) is believed to be a product of interior live oak and California black oak hybridization [9,10]. Interior live oak is described as morphologically "diverse," and a number of recognizable varieties or forms have been reported [9]. These taxa differ in such characteristics as leaf and acorn morphology, and general growth habit. Currently recognized varieties are as follows [3,5,6]: Quercus wislizenii var. frutescens Engelm. Quercus wislizenii var. wislizenii Quercus wislizenii forma extima Jeps. LIFE FORM : Tree, Shrub FEDERAL LEGAL STATUS : No special status OTHER STATUS : NO-ENTRY COMPILED BY AND DATE : D. Tirmenstein, August 1989 LAST REVISED BY AND DATE : D. Tirmenstein, June 1990 AUTHORSHIP AND CITATION : Tirmenstein, D. 1989. Quercus wislizenii. In: Remainder of Citation

DISTRIBUTION AND OCCURRENCE

SPECIES: Quercus wislizenii | Interior Live Oak
GENERAL DISTRIBUTION : Interior live oak occurs from Siskiyou and Shasta counties of northern California south along the foothills of the Sierra Nevada and inner Coast Ranges into northern Mexico [33,43,47]. It is common near the coast and on the Channel islands [68]. Interior live oak grows on approximately 884,000 acres (357,895 ha) in California [10]. The variety frutescens occurs throughout the mountains of southern California northward to Lake and Shasta counties. However, this variety is uncommon in the Sierra Nevada [40]. ECOSYSTEMS : FRES20 Douglas-fir FRES21 Ponderosa pine FRES26 Lodgepole pine FRES27 Redwood FRES28 Western hardwoods FRES34 Chaparral - mountain shrub STATES : CA MEXICO ADMINISTRATIVE UNITS : CHIS KICA PINN SAMO SEQU WHIS YOSE BLM PHYSIOGRAPHIC REGIONS : 1 Northern Pacific Border 2 Cascade Mountains 3 Southern Pacific Border 4 Sierra Mountains KUCHLER PLANT ASSOCIATIONS : K005 Mixed conifer forest K006 Redwood K029 California mixed evergreen forest K030 California oakwoods K033 Chaparral K034 Montane chaparral K035 Coastal sagebrush K037 Mountain mahogany - oak scrub SAF COVER TYPES : 232 Redwood 234 Douglas-fir - tanoak - Pacific madrone 237 Interior ponderosa pine 244 Pacific ponderosa pine - Douglas-fir 245 Pacific ponderosa pine 246 California blue oak 247 Jeffrey pine 248 Knobcone pine 249 Canyon live oak 250 Blue oak - Digger pine 255 California coast live oak SRM (RANGELAND) COVER TYPES : 201 Blue oak woodland 202 Coast live oak woodland 203 Riparian woodland 206 Chamise chaparral 207 Scrub oak mixed chaparral 208 Ceanothus mixed chaparral 209 Montane shrubland 422 Riparian HABITAT TYPES AND PLANT COMMUNITIES : This oak sometimes occurs in dense groves of small, evenly spaced individuals but also forms shrubby thickets within mixed-conifer forests [48]. It occurs below the mixed conifer zone in northern oak woodlands with such species as Oregon white oak (Quercus garryana), blue oak (Q. douglasii), valley oak (Q. lobata), canyon live oak (Q. chrysolepis), and gray pine (P. sabiniana) [4,17,27,28,38,65]. Interior live oak is an important component of certain riparian woodlands of California [30,51]. Interior live oak is well-represented in oak chaparral or montane chaparral dominated by such species as Nuttall's scrub oak (Q. dumosa) [2,4,29,39,53,61]. It also occurs in pinyon (Pinus spp.) woodlands and in humid conifer forests of the central California coast [10]. The variety frutescens is most closely associated with fairly xeric chaparral communities of southern California [11,17,56]. Interior live oak has been included in the following plant associations and community types: Vegetation types of the San Gabriel Mountains [29] Vegetation of the San Bernadino Mountains [39] A vegetation classification system applied to souther California [44] The vascular plant communities of California [61] An introduction to the plant communities of the Santa Ana and San Jacinto Mountains [68] Associated species: Other conifer or hardwood associates of interior live oak include coastal live oak (Quercus agrifolia), Douglas-fir (Pseudotsuga menziesii), Jeffrey pine (Pinus jeffreyi), redwood (Sequoia sempervirens), ponderosa pine (Pinus ponderosa), cottonwoods (Populus spp.), tanoak (Lithocarpus densiflorus), and Pacific madrone (Arbutus menziesii) [2,10,42]. Commonly associated understory species include manzanita (Arctostaphylos spp.), ceanothus (Ceanothus spp.), birchleaf mountain-mahogany (Cercocarpus betuloides), hazel (Corylus cornuta), two-petal ash (Fraxinus dipetala), toyon (Heteromeles arbutifolia), yerba santa (Eriodycton californicum), redberry (Rhamnus crocea), chamise (Adenostoma fasciculatum), poison-oak (Toxicodendron diversiloba), California redbud (Cercis occidentalis), sagebrush (Artemisia spp.), and rabbitbrush (Chrysothamnus spp.) [17]. Serviceberry (Amelanchier spp.), snowberry (Symphoricarpos spp.), raspberries (Rubus spp.), and oceanspray (Holodiscus discolor) are common plant associates in timbered areas [10].

VALUE AND USE

SPECIES: Quercus wislizenii | Interior Live Oak
WOOD PRODUCTS VALUE : Interior live oak is currently highly valued as firewood in many parts of California, and projections point to ever-increasing demands for oak (Quercus spp.) fuelwoods [37,47,53,65]. However, cordage per acre varies widely according to soils and climate [34]. The wood of interior live oak has little commercial value as lumber [44]. Undesirable characteristics such as poor durability limit its use [65]. IMPORTANCE TO LIVESTOCK AND WILDLIFE : Interior live oak provides important food and cover for a wide variety of birds and mammals. The following species, which occur within the range of interior live oak, feed on the foliage of oaks: black-tailed jackrabbit, Audubon cottontail, brush rabbit, Beechy ground squirrel, Sonoma chipmunk, beaver, porcupine, and elk [3]. Pocket gophers occasionally consume the cambium of young oaks [48]. In some areas, interior live oak is a valuable year-round deer browse [56]. The evergreen leaves can provide essential winter browse when other preferred foods are scarce [8]. However, winter utilization by Columbian black-tailed deer in the Sierra Nevada was reported at approximately 15 percent, suggesting that this oak is not a preferred browse species in this area [22]. Oak browse is generally most important to deer during the early spring when new sprouts are abundant [22,37]. In some areas deer use oak browse to a limited extent during the summer [37]. Oak woodlands offer good habitat for mountain lions because of the relatively large numbers of deer which frequent these areas [3]. Acorns, which become available by fall, are a valuable dietary supplement for deer and other wild ungulates [37]. However, acorn production varies annually, and in some years relatively few acorns are produced. Interior live oak does not generally produce acorns in great quantity [65], but larger crops are usually produced at 5- to 7-year intervals [43]. More deer move to winter ranges earlier in years of abundant acorn production than in years of acorn failure [32]. Acorns are an important food of the black-tailed jackrabbit, brush rabbit, Beechy ground squirrel, golden-mantled ground squirrel, lodgepole chipmunk, long-eared chipmunk, Sonoma chipmunk, Merriam chipmunk, Douglas squirrel, porcupine, red fox, gray fox, black bear, raccoon, striped skunk, spotted skunk, California ground squirrel, deer mice, California vole, and harvest mice [3,26]. Acorns represented a particularly important food source of the California grizzly bear prior to its extinction [26]. Many birds eat acorns including quails, ring-necked pheasant, northern flicker, acorn woodpecker, scrub jay, magpie, Steller's jay, mountain chickadee, California thrasher, western meadowlark, starling, purple finch, American goldfinch, rufous-sided towhee, brown towhee, common crow, and band-tailed pigeon [26,66]. Interior live oak provides good foraging sites for Nutall's woodpecker, white-breasted nuthatch, plain titmouse, ash-throated flycatcher, black-headed grosbeak, and northern oriole [9]. Livestock: Cattle and domestic sheep typically utilize interior live oak browse most during the late spring and summer [55,56]. Young shoots are particularly favored by cattle during the summer [55]. In some parts of California, the leaves of interior live oak, along with the leaves of other oaks, have been found in the diets of 60 percent or more of the sheep and cattle within the area [37]. Domestic goats apparently consume oak browse during all seasons [61], although young shoots are particularly sought in the spring [56]. Domestic and feral pigs consume large numbers of acorns wherever available [3]. PALATABILITY : The acorns and foliage of interior live oak are palatable to many birds and mammals. However, overall palatability of the foliage of interior live oak is described as fair. New sprouts appear to be much more palatable to most ungulates than the mature foliage. Deer eagerly seek out sprouts up to 2 years in age during all seasons [56]. Specific palatability ratings are as follows [3,19]: mast foliage mule deer moderate moderate wild boar heavy ---- brush mouse light light pinyon mouse light light California mouse light light deer mouse light light dusky-footed woodrat light light western gray squirrel heavy ---- Botta pocket gopher moderate moderate the variety frutescens - California cattle poor horses useless domestic sheep fair to useless domestic goats fair to poor deer excellent to good NUTRITIONAL VALUE : Acorns: Acorns are generally rated as relatively high in carbohydrates, fats, and crude fiber, but low in protein and ash [37,56]. The nutritional value of interior live oak acorns is as follows [1,19]: moisture crude crude fat N-free ash Ca tannins P (%) protein fiber (%) extract (%) (%) (%) (%) (%) (%) 29.80 3.08 11.24 14.47 40.40 1.01 0.09 4.60 0.05 Foliage: Oak browse is relatively high in protein and carbohydrates. However, tannins present in oak browse may reduce protein digestibility [37]. The composition of leafy branches is as follows [56]: total ash (%) silica (%) silica-free Ca P K ash (%) (%) (%) (%) 2.27 0.34 2.93 0.707 0.069 0.335 Protein levels of interior live oak browse vary seasonally as follows [56]: April and May 17.5% June - August 10.5% September - March 8.0% COVER VALUE : Interior live oak provides good thermal, escape, and resting cover for many birds and mammals. Larger California oaks (Quercus spp.) offer shade for livestock and good hiding cover for deer [56]. Dense oak chaparral made up of smaller shrublike oaks provides excellent thermal cover for animals such as the gray fox and bobcat. Raccoons use hollow oaks for dens, and black bears occasionally den at the base of trees. Fallen oaks serve as hiding locations for deer mice, striped skunks, gray squirrels, and fox squirrels. Interior live oak provides hiding, resting, or nesting cover for the following species: black-tailed jackrabbit, Audubon cottontail, brush rabbit, Beechy ground squirrel, golden-mantled ground squirrel, lodgepole chipmunk, long-eared chipmunk, Sonoma chipmunk, Merriam chipmunk, Douglas squirrel, San Joaquin pocket mouse, San Diego pocket mouse, spiny pocket mouse, Stephens kangaroo rat, San Joaquin kangaroo rat, giant kangaroo rat, desert woodrat, common opossum, shrews, bats, beaver, pinyon mouse, brush mouse, California mouse, deer mouse, cactus mouse, muskrat, Pacific jumping mouse, dusky-footed woodrat, Botta pocket gopher, western gray squirrel, porcupine, red fox, gray fox, island fox, black bear, ringtail, raccoon, spotted skunk, striped skunk, wild boar, mountain lion, mule deer, and elk [3]. Many birds use California oaks for perching and nesting sites. Some larger, older interior live oaks are well-suited for excavation by various cavity nesters [66]. VALUE FOR REHABILITATION OF DISTURBED SITES : Interior live oak has been used to a limited extent in revegetating certain riparian areas of California. Little sprouting was observed after acorns were planted onto riparian sites in the Santa Clara Valley of southern California, and viability may have been much reduced or lost while seeds were in storage [23]. OTHER USES AND VALUES : After leaching away the bitter tannins, Native Americans used the acorns of many oaks (Quercus spp.) for cooking oils, soups, stews, or breads [1]. Some California oaks were historically used locally as fenceposts or mine timbers. Many are currently used for landscaping purposes [56]. Interior live oak was first cultivated in 1874 [43]. MANAGEMENT CONSIDERATIONS : Wildlife management: For maintaining optimum wildlife value in California oak woodlands, managers recommend the following [3]: 1) maintain 25 to 50 percent canopy cover in oaks. 2) maintain basal area of 200 to 2,000 ft. sq. per 40 acres. 3) maintain a mixture of age classes. 4) disperse oaks in 0.5 to 5 acre aggregations. Avian diversity may be enhanced by retaining large patches of oak, leaving adequate travel corridors between patches, and keeping structural diversity within the patches [52]. Harvesting: Interior live oak may be well-suited for periodic harvesting for energy generation because of its high rate of biomass production and net primary productivity [50]. Chemical control: Interior live oak is resistant to most herbicides. Two or three treatments are often required for a complete kill [7]. Grazing: Biswell [6] reports that in areas dominated by interior live oak which are managed primarily for livestock production, deferred grazing may be undesirable. Browsing here serves as the main controlling factor in brush suppression.

BOTANICAL AND ECOLOGICAL CHARACTERISTICS

SPECIES: Quercus wislizenii | Interior Live Oak
GENERAL BOTANICAL CHARACTERISTICS : Interior live oak is a slow-growing, variable evergreen which grows as a large shrub or small tree [15,40,61]. Plants may reach 30 to 75 feet (10-22 m) in height or assume a shrublike growth form with maximum heights of only 8 to 10 feet (2.4-3.1 m). D.b.h. generally ranges from 1 to 3 feet (0.3-0.9 m) [47]. A maximum size of 85.3 inches (216.7 cm) d.b.h. and 90 feet (27.5 m) in height has been reported [10]. The gray-to-dark gray bark is smooth when young but becomes rough and broadly ridged at maturity [40,47]. Young twigs are green-to-reddish but become gray with age [15]. Roots can extend from 30 to 70 feet deep (10-21 m) [18,54]. Interior live oaks have been aged up to 150 to 200 years, although the root system is often much older [47]. In relatively open stands the crown is usually dense and full, and foliage often extends to the ground. However, crowns are often irregularly shaped in closed stands [47]. Leaves, which persist for 2 years, are mostly oblong-to-elliptic or lanceolate, and spiny-toothed to entire [40,47]. Both leaf surfaces are shiny green but the upper surface is darker [15,47]. Interior live oak is monoecious. Male flowers are borne in catkins 1 to 3 inches (2-5 cm) in length, whereas female flowers grow in clusters of two to four in the upper leaf axils [15]. The tan, often longitudinally striped acorns are slender, cylindrical to conical, with a turbinate cap [40]. The shrubby variety frutescens is characterized by stiff, rigid twigs and ovate or oblong leaves 0.8 to 1.6 inches (2.0-4.1 cm) in length [40,56]. Acorns are oblong-to-ovate and the cup is covered with thin brown scales [56]. RAUNKIAER LIFE FORM : Phanerophyte REGENERATION PROCESSES : Interior live oak regenerates vegetatively after disturbance and also reproduces through seed. Both modes of regeneration appear to be important, although the relative value of each depends on such factors as weather, seed disseminators, soils, and the type and intensity of disturbance. Seed: Mature acorns of interior live oak are slender, oblong to ovate, or pointed [15,40,47]. Cleaned acorns average approximately 125 per pound (275/kg). Annual seed production appears to be somewhat variable, although each interior live oak tree generally produces good seed crops at 5- to 7-year intervals [43]. The dry weight yields of fallen acorns in interior live oak stands range from 0 to 97 pounds per acre (0-109 kg/ha) [66]. Interior live oak produces an average of 958 pounds per acre (1,074 kg/ha) of tree canopy in good mast years but averages only 113 pounds per acre (614 kg/ha) in poor mast years [37]. Germination: Ripening time varies according to annual growing conditions and elevation [35,46]. Viable acorns have been picked as early as August 10, although these acorns did not germinate without prior stratification. Acorns collected 2 to 4 weeks later germinated without any additional treatment [46]. Germination is frequently delayed at higher elevations. It commonly occurs during late November through January at lower elevations but often does not take place until January or February at higher elevations [35]. Research indicates that the acorns of interior live oak can germinate without exposure to low temperatures [13,35]. However, exposure to temperatures of 32 to 41 degrees F (0-5 degrees C) can effectively stratify seed and enhance germination [13,16]. Results of germination tests are as follows [43]: cold stratification temperature F duration germination (days) day night (days) capacity (%) 30 to 60 86 68 69 75 In laboratory tests, 50 percent of all acorns germinated within 40 days after exposure to temperatures of 55 to 68 degrees F (13-20 degrees C) without prior stratification [35]. Acorns are not noted for long viability. Some acorns of interior live oak germinate after 6 to 12 months of storage, but many exhibit damage or deformity [46]. Seed dispersal and mortality: Gravity and animal vectors aid in the dispersal of interior live oak. Squirrels and jays appear to be particularly important dispersal agents, although they consume many acorns. Acorns are vulnerable to predation and nearly 100 percent of the acorns may be consumed where deer, pigs, or bear occur [3]. Acorns are also susceptible to rot, insects, and disease. Mortality of planted interior live oak acorns ranged from 2 to 27 percent under carefully controlled laboratory experiments [35]. Vegetative regeneration: Interior live oak sprouts vigorously after fire or mechanical disturbance [15,22,44]. Root crown sprouting frequently occurs after damage to the trunk or crown [47]. Stump-sprouting is also common after fire or timber harvest [10,15]. Sprout growth of interior live oak is described as "moderate at best" [P. McDonald, pers. comm. 1990]. SITE CHARACTERISTICS : Interior live oak most commonly grows scattered in valleys, foothills, or on slopes at low to middle elevations [35,40]. It is often found in canyon bottoms and dry washes of southern California [48] and on broad alluvial banks of rivers in the Sierra Nevada [47]. Elevation: Generalized elevational ranges of interior live oak are as follows [35,47]: from 1,000 to 2,000 feet (300-600 m) in northern CA up to 6,200 feet (1,300 m) in southern CA from 3,950 to 4,950 feet (1,200-1,500 m) in Sierra Nevada, CA from 200 to 1,950 feet (60-600 m) in Santa Lucia Mtns., CA Soils: California oaks generally grow well on a variety of soils including well-drained, fine-grained to cobbly or gravelly sandy loams, or skeletal soils. Soil pH generally ranges between 5.6 and 7.5, with common soil depths of 20 to 40 inches (50-100 cm) [48]. Interior live oak grows particularly well on dry, shallow, well-drained loams, clay loams, gravelly loams, or gravel [12,27,34,65]. SUCCESSIONAL STATUS : Interior live oak is tolerant of shade, particularly when young [47], and occurs within the understory of some climax conifer forests of California. Cooper [17] reported that the variety frutescens is especially common in climax chaparral communities which are maintained by fire. Interior live oak is a prolific sprouter and can also assume prominence in some early seral communities. SEASONAL DEVELOPMENT : Interior live oak flowers from March to May [40]. Acorns mature in the second year [12]. Ripening time varies annually and depends largely on elevation and growing conditions. Acorns generally ripen after mid-August [46]. Immature acorns of live oaks which are poorly developed, or which have been damaged by rain, hail, wind, or insects may begin to fall as early as May [35]. Mature acorns are dispersed in late summer or fall.

FIRE ECOLOGY

SPECIES: Quercus wislizenii | Interior Live Oak
FIRE ECOLOGY OR ADAPTATIONS : Interior live oak appears to be well-adapted to persist with or without fire. It occupies fire-prone chaparral but also grows in relatively mesic areas which burn at infrequent intervals. Large, single-stemmed trees are generally only found in areas which have not burned in 50 to 100 years. Shrubby interior live oak is common in chaparral, where fairly frequent fires produce dense thickets of multi-stemmed individuals [44]. The shrubby growth form may represent an adaption to fire. These shrubby plants tend to reach sexual maturity at an earlier age than treelike growth forms [13]. The trait of "evergreeness" allows species such as interior live oak to allocate greater amounts of energy to regeneration than to vegetative growth. Evergreens are often better able to conserve available nutrients than deciduous species, and may be favored in these fire-prone settings [36]. Interior live oak often grows as a dominant on relatively mesic northern exposures in oak (Quercus spp.) chaparral. Here it grows fairly rapidly and soon reaches sufficient height to shade out most postfire seeding species [38]. The prominence of sprouters such as interior live oak in drier chaparral communities does not necessarily imply that these plants possess specific fire adaptations, but that they are better generalists in these arid habitats than are most postfire seeders [36]. Aboveground portions of interior live oak are described as sensitive to fire [44], and plants are generally top-killed. The thin bark and small diameter typical of this species offer little protection [24,45]. However, plants generally sprout prolifically from the stump and root crown after fire or other disturbance [10,15,47]. Postfire seedling establishment can also occur [69], although success may be highly dependent on weather conditions. POSTFIRE REGENERATION STRATEGY : Tree with adventitious-bud root crown/soboliferous species root sucker Initial-offsite colonizer (off-site, initial community)

FIRE EFFECTS

SPECIES: Quercus wislizenii | Interior Live Oak
IMMEDIATE FIRE EFFECT ON PLANT : Trunks and crowns of interior live oak are extremely sensitive to fire [44,47]. However, because of this oak's ability to sprout after fire, plants usually survive even when aboveground vegetation is consumed. Interior live oak is generally top-killed whenever fuels burn around the base of the tree [24]. The total effect of fire on oaks varies according to fire intensity and severity, fire behavior, season of burn, and size of the plants [45,47]. Generally, late season fires are more damaging to oaks than those which occur in the spring. Winter fires appear to cause the least damage. Slower moving, lower intensity fires are typically more damaging to the trunk than fires of higher intensity but shorter duration. Crowns are most susceptible to fires of higher intensity, even if they are of short duration. Bark is typically less severely damaged when burned at lower ambient air temperatures. Oaks less than 6 inches (15.2 cm) d.b.h. are generally top-killed by even low intensity fires [47]. Younger trees, and those with smaller diameters and lower crown heights tend to be most susceptible. In comparison with other oaks, interior live oak has a high ratio of inner to outer bark, but total bark thickness is low and offers little protection. Researchers observed that even interior live oaks with a bark thickness of 1 inch (2.5 cm) or more were girdled at the base after a fire of moderate intensity. Most California interior live oaks have a d.b.h. of less than 12 inches (30.5 cm) which further increases vulnerability to fire [45]. Stem and bark: Young oak stems which have been damaged by heat generally change from a gray to reddish-gray in color. The subsurface layer of the bark changes from a green to tan or brown, and inner bark appears yellow instead of the normal white or pink. Damaged inner bark often develops a characteristic fermented aroma [47]. When the bark of interior live oak is charred, cambium death is almost inevitable [45]. The cambium can be considered dead if the bark has been consumed, or if it appears to be cracked and separated from the wood. Trunk char may be categorized as follows [47]: light charring - spotty char or scattered pitting of the bark. medium charring - continuous charing, areas of minor bark reduction. heavy charring - pronounced reductions in bark thickness, wood sometimes exposed. Crown: Crown damage is variable in oaks and the degree of damage can differ even within an individual crown [45]. The extent of damage may range from none to total removal of the foliage. The actual extent of damage is not always readily apparent in oaks. A period of several years may be required for the full extent of damage to become evident. [See Discussion and Qualification of Fire Effect]. Fire-related injuries can increase oak's susceptibility to attack by insects, fungus, or windthrow [45]. Although portions of most interior live oaks survive after plants are top-killed by fire, some are killed if burned too frequently [48]. Acorns are extremely sensitive to heat [45] and are generally killed even when buried in the soil, litter, or duff. DISCUSSION AND QUALIFICATION OF FIRE EFFECT : The full effect of fire on interior live oak may not become obvious for some time. It may be necessary to wait at least one growing season, and preferably three, before the amount of injury can be accurately determined. Trees with bark as thick as 1.5 to 2.0 inches (3.8-5.1 cm) can be girdled, although initial visual examination suggests that the bark has received only minor charring. The surface of even heavily charred interior live oak remains smooth and often retains the original furrow patterns. As the bark dries, vertical cracks may appear, exposing the damaged tissue beneath [47]. Various methods have been developed for assessing damage to oaks including chemical, electrical, and visual techniques [45,47]. PLANT RESPONSE TO FIRE : Interior live oak sprouts vigorously after the trunk or crown has been damaged by fire [8,22,56,60]. This oak sprouts from the stump [10,15] when remaining portions are sufficiently undamaged, and from the base or root crown [44,47]. Root crown sprouting, after damage to the trunk and crown, is generally vigorous [47]. Under some circumstances, postfire regeneration from seed may also occur [10,69], although acorns are vulnerable to heat [45]. Favorable weather conditions are necessary for good germination, and sprouting appears to be the primary mode of regeneration in most areas. Repeated fires generally produce small multistemmed trees [47]. Postfire recovery: Initial sprout growth is slow [16, P. McDonald, pers. comm. 1990], although Biswell and Gilman [8] reported that in the western Sierra Nevada of northern California, sprouts reached 24.9 inches (63 cm) in height within 10 or 11 months after fire. By the end of the second growing season, maximum sprout heights of 78 inches (198 cm) were reported, and a few sprouts had grown to 95 inches (241 cm) in height by the third summer. Maximum sprout heights of 8 feet 9 inches (267 cm) were observed by the fourth postfire growing season [1]. Oak (Quercus spp.) chaparral dominated by interior live oak (variety frutescens) and Nuttall's scrub oak (Q. dumosa) develop impenetrable cover within 5 to 10 years after fire [39]. Canopy cover of interior live oak is initially reduced by fire although actual oak numbers typically increase. Vogl [67] observed the following response of interior live oak in a recently burned knobcone pine (Pinus attenuata) forest of southern California: % cover # plants per acre unburned 5.4 88 burned 4.5 173 DISCUSSION AND QUALIFICATION OF PLANT RESPONSE : NO-ENTRY FIRE MANAGEMENT CONSIDERATIONS : Fuels and flammability: The heat content and flammability of interior live oak has been calculated as follows [45]: (theoretical value for heat of combustion = 8,600 Btu/lb.) density (lb/cu ft) heat content (Btu/lb) outer bark 62 9,875 inner bark 45 7,700 wood 44 7,925 Prescribed fire: Plumb [45] reports "successful use of prescribed fire in interior live oak management does not seem promising" where maintenance of woodlands is a primary management goal. Poor heat resistance and easily damaged bark generally result in stem mortality or damage producing high potential for decay [11, P. McDonald, pers. comm. 1990]. Large individual trees may feasibly be protected in small areas [45]. Repeated fires may be used to maintain this oak as a small multistemmed plant [47]. Postfire harvest: A correct determination of the degree of damage is essential before appropriate harvest recommendations can be made. Plumb and Gomez [47] suggest waiting at least one growing season, and if possible three, before cutting larger valuable trees which have uncertain potential for crown survival. Once damage has been assessed, the following guidelines may be used [45]: tree size and degree of trunk char - light medium heavy < 6 inches dbh cut cut cut 6-12 inches dbh leave cut cut > 12 inches dbh leave cut cut Harvesting may be recommended if 75 percent of the trunk is girdled on trees less than 6 inches (15.2 cm) d.b.h., or if more than 50 percent is girdled on trees greater than 6 inches d.b.h. [45]. Valley oak savannas: Certain higher elevation valley oak (Q. lobata) savannas in the Santa Lucia Mountains of central coastal California, are being invaded by species such as interior live oak. Fire suppression is frequently cited as a probable cause of this vegetative shift. Although seedlings of both oaks are eaten by herbivores, interior live oak sprouts tend to be somewhat more browse-resistant. Increased livestock utilization may favor interior live oak. Frequent fires presumably killed many of the young interior live oak sprouts and helped to maintain valley oak savanna [26]. Wildlife and livestock: Sprouts are extremely vulnerable to herbivores during the first few years after fire [22,25,56]. Domestic goats can kill a large proportion of sprouts and seedlings during the first 3 to 5 years after fire. Deer prefer oak sprouts and feed on them year-round for at least the first 2 postfire years [56]. Fire in California oak woodlands can create favorable, although transitory, habitat for birds such as the flicker and hairy woodpecker which feed on insects present in the branches of fire-killed trees [14].

REFERENCES

SPECIES: Quercus wislizenii | Interior Live Oak
REFERENCES : 1. Bainbridge, David A. 1987. The use of acorns for food in California: past, present, future. In: Plumb, Timothy R.; Pillsbury, Norman H., technical coordinators. Proceedings of the symposium on multiple-use management of California's hardwood resources; 1986 November 12-14; San Luis Obispo, CA. Gen. Tech. Rep. PSW-100. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 453-458. [5395] 2. Barbour, Michael G. 1987. Community ecology and distribution of California hardwood forests and woodlands. In: Plumb, Timothy R.; Pillsbury, Norman H., technical coordinators. Proceedings of the symposium on multiple-use management of California's hardwood resources; 1986 November 12-14; San Luis Obispo, CA. Gen. Tech. Rep. PSW-100. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 18-25. [5356] 3. Barrett, Stephen W. 1980. Indians & fire. 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Prescribed burning program for the coastal redwoods and chaparral. In: Mooney, Harold A.; Conrad, C. Eugene, technical coordinators. Proc. of the symposium on the environmental consequences of fire and fuel management in Mediterranean ecosystems; 1977 August 1-5; Palo Alto, CA. Gen. Tech. Rep. WO-3. Washington, DC: U.S. Department of Agriculture, Forest Service: 397-403. [4869] 26. Griffin, James R. 1976. Regeneration in Quercus lobata savannas, Santa Lucia Mountains, California. American Midland Naturalist. 95(2): 422-435. [4775] 27. Griffin, James R. 1977. Oak woodland. In: Barbour, Michael G.; Malor, Jack, eds. Terrestrial vegetation of California. New York: John Wiley and Sons: 383-415. [7217] 28. Griffin, James R.; Critchfield, William B. 1972. The distribution of forest trees in California. Res. Pap. PSW-82. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station. 118 p. [1041] 29. Hanes, Ted L. 1976. Vegetation types of the San Gabriel Mountians. In: Latting, June, ed. Symposium proceedings: plant communities of southern California; 1974 May 4; Fullerton, CA. Special Publication No. 2. Berkeley, CA: California Native Plant Society: 65-76. [4227] 30. Katibah, Edwin F.; Nedeff, Nicole E.; Dummer, Kevin J. 1984. Summary of riparian vegetation aerial and linear extent measurements from the Central Valley Riparian Mapping Project. In: Warner, Richard E.; Hendrix, Kathleen M., eds. California riparian systems: Ecology, conservation, and productive management: Proceedings of the conference; 1981 September 17-19; Davis, CA. Berkeley, CA: University of California Press: 46-50. [5824] 31. 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] 32. Leach, Howard R.; Hiehle, Jack L. 1956. Food habits of the Tehama deer herd. California Fish and Game. 43: 161-178. [6874] 33. Little, Elbert L., Jr. 1979. Checklist of United States trees (native and naturalized). Agric. Handb. 541. Washington, DC: U.S. Department of Agriculture, Forest Service. 375 p. [2952] 34. Lytle, Dennis J.; Finch, Sherman J. 1987. Relating cordwood production to soil series. In: Plumb, Timothy R.; Pillsbury, Norman H., technical coordinators. Proceedings of the symposium on multiple-use management of California's hardwood resources; 1986 November 12-14; San Luis Obispo, CA. Gen. Tech. Rep. PSW-100 w. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 260-267. [5380] 35. Matsuda, Kozue; McBride, Joe R. 1987. Germination and shoot development of seven California oaks planted at different elevations. In: Plumb, Timothy R.; Pillsbury, Norman H., technical coordinators. Proceedings of the symposium on multiple-use management of California's hardwood resources; 1986 November 12-14; San Luis Obispo, CA. Gen. Tech. Rep. PSW-100. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 79-85. [5400] 36. McDonald, Philip M. 1981. Adapatations of woody shrubs. In: Hobbs, S. D.; Helgerson, O. T., eds. Reforestation of skeletal soils: Proceedings of a workshop; 1981 November 17-19; Medford, OR. Corvallis, OR: Oregon State University, Forest Research Laboratory: 21-29. [4979] 37. Menke, John W.; Fry, Michael E. 1980. Trends in oak utilization--fuelwood, mast production, animal use. In: Plumb, Timothy R., technical coordinator. Proceedings of the symposium on the ecology, management, and utilization of California oaks; 1979 June 26-28; Claremont, CA. Gen. Tech. Rep. PSW-44. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 297-305. [7050] 38. Minnich, R.; Howard, L. 1984. Biogeography and prehistory of shrublands. In: DeVries, Johannes J., ed. Shrublands in California: literature review and research needed for management. Contribution No. 191. Davis, CA: University of California, Water Resources Center: 8-24. [4998] 39. Minnich, Richard A. 1976. Vegetation of the San Bernardino Mountains. In: Latting, June, ed. Symposium proceedings: plant communities of southern California; 1974 May 4; Fullerton, CA. Special Publication No. 2. Berkeley, CA: California Native Plant Society: 99-124. [4232] 40. Munz, Philip A. 1973. A California flora and supplement. Berkeley, CA: University of California Press. 1905 p. [6155] 41. Munz, Philip A. 1974. A flora of southern California. Berkeley, CA: University of California Press. 1086 p. [4924] 42. Myatt, Rodney G. 1980. Canyon live oak vegetation in the Sierra Nevada. In: Plumb, Timothy R., technical coordinator. Proceedings of the symposium on the ecology, management and utilization of California oaks; 1979 June 26-28; Claremont, CA. Gen. Tech. Rep. PSW-44. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 86-91. [7019] 43. Olson, David F., Jr. 1974. Quercus L. oak. In: Schopmeyer, C. S., ed. Seeds of woody plants in the United States. Agric. Handb. 450. Washington, DC: U.S. Department of Agriculture, Forest Service: 692-703. [7737] 44. Paysen, Timothy E.; Derby, Jeanine A.; Black, Hugh, Jr.; [and others]. 1980. A vegetation classification system applied to southern California. Gen. Tech. Rep. PSW-45. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station. 33 p. [1849] 45. Plumb, Tim R. 1980. Response of oaks to fire. In: Plumb, Timothy R., technical coordinator. Proceedings of the symposium on the ecology, management, and utilization of California oaks; 1979 June 26-28; Claremont, CA. Gen. Tech. Rep. PSW-44. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 202-215. [7039] 46. Plumb, Timothy R. 1982. Factors affecting germination of southern California oaks. In: Conrad, C. Eugene; Oechel, Walter C., technical coordinators. Proceedings of the symposium on dynamics and management of Mediterranean-type ecosystems; 1981 June 22-26; San Diego, CA. Gen. Tech. Rep. PSW-58. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 625. [6093] 47. Plumb, Timothy R.; Gomez, Anthony P. 1983. Five southern California oaks: identification and postfire management. Gen. Tech. Rep. PSW-71. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station. 56 p. [5898] 48. Plumb, Timothy R.; McDonald, Philip M. 1981. Oak management in California. Gen. Tech. Rep. PSW-54. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station. 11 p. [6568] 49. Raunkiaer, C. 1934. The life forms of plants and statistical plant geography. Oxford: Clarendon Press. 632 p. [2843] 50. Riggan, Philip J.; Dunn, Paul H. 1982. Harvesting chaparral biomass for energy--an environmental assessment. In: Conrad, C. Eugene; Oechel, Walter C., technical coordinators. Proceedings of the symposium on dynamics and management of Mediterranean-type ecosystems; 1981 June 22-26; San Diego, CA. Gen. Tech. Rep. PSW-58. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 149-157. [6019] 51. Roberts, R. Chad. 1984. The transitional nature of northwestern California riparian systems. In: Warner, Richard E.; Hendrix, Kathleen M., eds. California riparian systems: Ecology, conservation, and productive management: Proceedings of the conference; 1981 September 17-19; Davis, CA. Berkeley, CA: University of California Press: 85-91. [5828] 52. Roberts, R. Chad. 1987. Preserving oak woodland bird species richness: suggested guidelines from geographical ecology. In: Plumb, Timothy R.; Pillsbury, Norman H., technical coordinators. Proceedings of the symposium on multiple-use management of California's hardwood resources; 1986 November 12-14; San Luis Obispo, CA. Gen. Tech. Rep. PSW-100. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 190-197. [5374] 53. Rossi, Randall S. 1980. History of cultural influences on the distribution and reproduction of oaks in California. In: Plumb, Timothy R., technical coordinator. Proceedings of the symposium on the ecology, management and utilization of California oaks; 1979 June 26-28; Claremont, CA. Gen. Tech. Rep. PSW-44. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 7-18. [7010] 54. Rundel, Philip W. 1980. Adaptations of Mediterranean-climate oaks to environmental stress. In: Plumb, Timothy R., technical coordinator. Proceedings of the symposium on the ecology, management and utilization of California oaks; 1979 June 26-28; Claremont, CA. Gen. Tech. Rep. PSW-44. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 43-54. [7014] 55. Sampson, Arthur W. 1944. Plant succession on burned chaparral lands in northern California. Bull. 65. Berkeley, CA: University of California, College of Agriculture, Agricultural Experiment Station. 144 p. [2050] 56. Sampson, Arthur W.; Jespersen, Beryl S. 1963. California range brushlands and browse plants. Berkeley, CA: University of California, Division of Agricultural Sciences, California Agricultural Experiment Station, Extension Service. 162 p. [3240] 57. Shiflet, Thomas N., ed. 1994. Rangeland cover types of the United States. Denver, CO: Society for Range Management. 152 p. [23362] 58. Sidahmed, Ahmed E.; Morris, James G.; Radosevich, Steven; Koong, Ling J. 1982. Seasonal changes in chaparral composition and intake by Spanish goats. In: Conrad, C. Eugene; Oechel, Walter C., technical coordinators. Proceedings of the symposium on dynamics and management of Mediterranean-type ecosystems; 1981 June 22-26; San Diego, CA. Gen. Tech. Rep. PSW-58. Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: 258-263. [6027] 59. Stickney, Peter F. 1989. Seral origin of species originating in northern Rocky Mountain forests. Unpublished draft on file at: U.S. Department of Agriculture, Forest Service, Intermountain Research Station, Fire Sciences Laboratory, Missoula, MT; RWU 4403 files. 7 p. [20090] 60. Sweeney, James R. 1956. Responses of vegetation to fire: A study of the herbaceous vegetation following chaparral fires. Berkeley, CA: University of California Press. 249 p. [3776] 61. Thorne, Robert F. 1976. The vascular plant communities of California. In: Latting, June, ed. Symposium proceedings: plant communities of southern California; 1974 May 4; Fullerton, CA. Special Publication No. 2. Berkeley, CA: California Native Plant Society: 1-31. [3289] 62. Tucker, John M. 1980. Taxonomy of California oaks. In: Plumb, Timothy R., technical coordinator. Proceedings of the symposium on the ecology, management and utilization of California oaks; 1979 June 26 - June 28; Claremont, CA. Gen. Tech. Rep. PSW-44. 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Related categories for Species: Quercus wislizenii | Interior Live Oak

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