Wildlife, Animals, and Plants
|
|
Introductory
SPECIES: Cercidium microphyllum | Yellow Paloverde
ABBREVIATION :
CERMIC
SYNONYMS :
Parkinsonia microphylla Torr. [52,80,88]
SCS PLANT CODE :
CEMI2
COMMON NAMES :
yellow paloverde
little-leaf paloverde
foothill paloverde
TAXONOMY :
The currently accepted scientific name of yellow paloverde is Cercidium
microphyllum (Torr.) Rose & Johnston [31,100]. It is a member of the
bird-of-paradise family (Caesalpinaceae) [26]. There are no recognized
infrataxa.
Yellow paloverde occasionally forms hybrids throughout its range with
blue paloverde (Cercidium floridum) [52]. In Mexico, yellow paloverde
hybridizes with Cercidium praecox to form Sonoran paloverde (C. x
sonorae) [43,93].
LIFE FORM :
Tree, Shrub
FEDERAL LEGAL STATUS :
No special status
OTHER STATUS :
NO-ENTRY
COMPILED BY AND DATE :
Diane S. Pavek, June 1994
LAST REVISED BY AND DATE :
NO-ENTRY
AUTHORSHIP AND CITATION :
Pavek, Diane S. 1994. Cercidium microphyllum. In: Remainder of Citation
DISTRIBUTION AND OCCURRENCE
SPECIES: Cercidium microphyllum | Yellow Paloverde
GENERAL DISTRIBUTION :
Yellow paloverde is distributed through central and southwestern Arizona
[16,31,43,88]. A few populations occur in southeastern California near
the Colorado River in the Whipple Mountains [3,10,26]. The range of
yellow paloverde extends southward through Sonora and Baja California,
Mexico [37,38,65,78,80,100].
ECOSYSTEMS :
FRES30 Desert shrub
FRES40 Desert grasslands
STATES :
AZ CA MEXICO
ADMINISTRATIVE UNITS :
DEVA LAME ORPI SAGU
BLM PHYSIOGRAPHIC REGIONS :
7 Lower Basin and Range
KUCHLER PLANT ASSOCIATIONS :
K041 Creosotebush
K042 Creosotebush - bursage
K043 Paloverde - cactus shrub
SAF COVER TYPES :
242 Mesquite
SRM (RANGELAND) COVER TYPES :
NO-ENTRY
HABITAT TYPES AND PLANT COMMUNITIES :
Yellow paloverde is an indicator species of the Sonoran Desert floristic
region [50]. It is a dominant species in the Arizona upland subdivision
of the Sonoran Desert [9,41,43,93]. Codominant species include
creosotebush (Larrea tridentata), triangle bursage (Ambrosia deltoidea),
brittle brush (Encelia farinosa), ocotillo (Fouqueria splendens), and
Berlandier wolfberry (Lycium belandieri) [9]. This assemblage is also
called the paloverde, bursage (Ambrosia spp.) desert scrub community
type. It grades into spinose suffrutescent desert scrub [54].
A major climax association found on bajadas and rocky slopes throughout
the Sonoran Desert is the paloverde/saguaro (Carnegiea gigantea)
association [5,9,42,89,102]. This association grades into adjacent
semidesert grasslands and interior chaparral [53,54].
Yellow paloverde is the principal species in the paloverde series
[51,61]. This is also called the paloverde-cacti-mixed scrub series and
paloverde woodland and succulents association [93,103].
Yellow paloverde is a facultative riparian species. It may move into
riparian areas from surrounding desert and upland positions [1,74,83].
Where precipitation is less than 3 inches (7.6 cm) per year, yellow
paloverde is confined to washes and is an obligate riparian species [2].
Yellow paloverde is listed as a dominant or indicator species in the
following publications:
(1) A series vegetation classification for Region 3 [51]
(2) A vegetation classification system applied to southern California
[61]
(3) Vegetation of the Santa Catalina Mountains, Arizona: a gradient
analysis of the south slope [99].
Species associated with yellow paloverde but not previously mentioned in
DISTRIBUTION AND OCCURRENCE include white burrobrush (Hymenoclea
salsola), white ratany (Krameria grayi), organpipe cactus
(Lemaireocereus schottii), MacDougal ocotillo (Fouqueria macdougalii),
and heart leatherstem (Jatropha cordata) [25,78,97].
VALUE AND USE
SPECIES: Cercidium microphyllum | Yellow Paloverde
WOOD PRODUCTS VALUE :
The wood of yellow paloverde is hard and heavy [37].
IMPORTANCE TO LIVESTOCK AND WILDLIFE :
Yellow paloverde has limited value as browse for livestock [3,28,87].
Bighorn sheep, mule deer, and feral burros browse yellow paloverde
[25,34,63,75,76]. It is important browse for jackrabbits, heteromyid
rodents, and other small mammals [16,25,67,96]. Collared peccary
consume yellow paloverde fruits from July to September [15]. Yellow
paloverde was used significantly (P<0.01) more than other plant species
for foraging by birds [58].
Small mammals such as desert shrews and mice use the habitats where
yellow paloverde occurs [86].
PALATABILITY :
NO-ENTRY
NUTRITIONAL VALUE :
Several studies have sampled yellow paloverde bimonthly for 1 year. Its
leaves, flowers, and new growth had from 30 to 60 percent dry matter and
from 6 to 16 percent crude protein [34,63,76]. Yellow paloverde has
large seeds that weigh an average of 0.005 ounce (0.147 g) and contain
733.3 calories per seed [68].
COVER VALUE :
Yellow paloverde that are taller than 6.6 feet (2 m) are used for
nesting [89]. Verdin and black-tailed gnatcatchers nest in yellow
paloverde [58]. Gambel's quail use them for roosts [23]. Yellow
paloverde snags are important wildlife habitat because snags occur
infrequently in the Sonoran Desert. In Arizona, nine bird species used
one yellow paloverde snag daily [32].
White-throated woodrats use yellow paloverde for shelter or nests [57].
VALUE FOR REHABILITATION OF DISTURBED SITES :
Yellow paloverde was used in the revegetation of an open pit copper mine
in Arizona. Yellow paloverde survived significantly (P<0.05) better on
the east slope (27 plants/244 sq m) than on the north slope (1 plant/244
sq m) [56].
OTHER USES AND VALUES :
Yellow paloverde seeds were ground and used for food by Pima and other
Native Americans [37,66].
Yellow paloverde is planted as an ornamental [37].
MANAGEMENT CONSIDERATIONS :
Dimensional analyses that relate fresh biomass to stem diamter and dry
matter content are available for yellow paloverde [18].
Yellow paloverde was evaluated as a potential energy-producing crop.
During 2 years of sampling, the stems, leaves, and fruits of yellow
paloverde yielded moderate amounts of oil and crude protein. It was not
considered a promising species for exploitation [11].
Yellow paloverde spread from residential plantings into surrounding
wildlands in Death Valley National Monument, California. Yellow
paloverde does not occur there naturally, and mechanical and herbicide
control methods have been proposed to eradicate it [40].
Yellow paloverde and other desert scrub species invade desert grasslands
following disturbances such as grazing [40,98].
Yellow paloverde up to 3 inches (7.6 cm) tall may be seriously injured
or killed by jackrabbit browsing. Larger trees are browsed to the
extent that a jackrabbit can reach, about 3 feet (1 m) [96].
Yellow paloverde is an alternate host for seed-predating bruchid
beetles (Mimosestes spp.). Yellow paloverde responses are probably
similar to those of the beetles' primary host, mesquite (Prosopis spp.),
with reduced yields of viable seeds [33].
Yellow paloverde and community associates typical of the Arizona upland
subdivision of the Sonoran Desert occur in very few places in
southeastern California. This is a community type with one of the
highest priorities in California for rare plant inventories [27].
Yellow paloverde provides canopy cover that reduces maximum soil surface
temperatures. This is important for the establishment of other desert
species [20,78]. Yellow paloverde is the primary nurse plant for
saguaro [14,30,43,55,84].
BOTANICAL AND ECOLOGICAL CHARACTERISTICS
SPECIES: Cercidium microphyllum | Yellow Paloverde
GENERAL BOTANICAL CHARACTERISTICS :
Yellow paloverde is a native, monoecious, spiny shrub or small tree that
may grow to 26 feet (8 m) tall [3,37,52,88]. The trunk may be 1 foot
(0.3 m) in diameter; it branches about 8 inches (20 cm) from the ground
into four to six major stems [57]. The crown spreads 12 to 18 feet
(3.7-5.5 m) [32]. The bark is thin and photosynthetic [91]. Yellow
paloverde has numerous flowers in 1 inch (2.5 cm) long clusters [16,37].
It has pinnately compound leaves about 1 inch (2.5 cm) long with minute
leaflets and is drought-deciduous [37,100]. Fruits are 2 to 3 inches
(4-8 cm) long and have one to five seeds with constrictions between the
seeds [16,37,80].
Yellow paloverde lives longer than 72 years [22].
Yellow paloverde is susceptible to freezing [90].
RAUNKIAER LIFE FORM :
Phanerophyte
REGENERATION PROCESSES :
Yellow paloverde reproduces sexually and asexually. Yellow paloverde
has fair to poor ability to produce sprouts after top removal [11].
Photoperiod initiates fruit and flower production of yellow paloverde.
Subsequent local weather conditions determine whether flowering or seed
set occurs [91]. A seed crop is produced when the spring is wet or very
cool [105].
Yellow paloverde is insect pollinated [44,82].
McAuliffe [47] stated that yellow paloverde pods rapidly abscise as a
mechanism to avoid seed predation by bruchid beetles. The constricted
fruits of yellow paloverde do not open before dispersing [37].
Seeds germinate during a rainy season after 1 year in the soil.
Seedlings are very susceptible to drought during the first 2 to 3 months
following germination. During a 9-year study in Arizona, 1.6 percent of
all seedlings that germinated survived [105].
Recruitment of yellow paloverde is very slow. Additions as low as two
individuals over 30 years or longer have been recorded [22,79].
Herbivory limits yellow paloverde distribution [45]. Bruchid beetles
are seed predators of yellow paloverde [47]. Heteromyid rodents rapidly
cache yellow paloverde seeds. The cached seeds occasionally germinate
[47,95].
Initial distributions of yellow paloverde seedlings are random.
However, after 1 year, a greater proportion of seedlings in open spaces
were consumed by rabbits and hares than seedlings beneath triangle
bursage. Recruitment patterns of yellow paloverde show significantly
(P<0.001) positive associations with mature triangle bursage and white
bursage (Ambrosia dumosa) [45,46]. Because yellow paloverde outlives
triangle bursage, large mature yellow paloverde have no association with
triangle bursage [46].
Unpredictable water availability causes low, erratic seedling
establishment [12]. Mature yellow paloverde maintain deep root contact
with wet soil [73,105]. Yellow paloverde self prunes; large branches
die during drought [3,105]. Young plants usually survive drought once
they drop branches which occurs at variable ages [77,105]. Death of
mature yellow paloverde due to drought and subsequent desiccation is
uncommon [45,77,92]. Based on water requirement trials, the water-use
efficiency of yellow paloverde approaches that of perennial grasses
[48].
SITE CHARACTERISTICS :
Yellow paloverde occurs in arid to semiarid climates with mild winters
and hot summers; precipitation is bimodal, occuring in summer and fall [15,54].
Yellow paloverde is found on lower mountain slopes and alluvial outwash
plains [54,97]. In the most arid parts of its range, yellow paloverde
occasionally occurs in small washes or arroyos [24,59,64,91,97].
Yellow paloverde occurs from 1,000 to 4,000 feet (305-1,219 m) in
elevation throughout its range [19,23,54,97,99]. It grows on very
gradual to steep slopes that may face south or north, but it has been
reported on all aspects [19,24,28,36,60,101].
The sites on which yellow paloverde occurs are well-drained [28].
Surface soils may be 1.6 to 2.8 inches (4-7 cm) thick and subsoils may
be 20 inches (50 cm) thick over caliche [91,101]. The soil temperature
regime is thermic (that is, average soil temperatures are between 59 and
72 degrees Fahrenheit [15-22 deg C]) [51]. Soil textures range from
sand to sandy loam to loam [24]. They may be underlain by clay loam and
clays [23,89]. Parent materials may be basaltic, rhyolitic, granitic,
mixed alluvium, and metamorphic [22,49,59,60,91].
The distribution of yellow paloverde is influenced by the continuum of
soil textures that occurs from upper to lower bajada [5]. It is found
primarily on the upper bajadas [6,7,93,97]. Coarse soil of the upper
bajada has one-half the wilting coefficient (which is an estimate of
plant stress) of the finer soil of the lower bajada [102]. Yellow
paloverde grows infrequently on the middle and lower bajada [97].
SUCCESSIONAL STATUS :
Facultative Seral Species
Yellow paloverde is a climax species in the Sonoran Desert flora [51,54,61].
Successional sequences have not been completely identified for the
desert scrub communities in which yellow paloverde occurs. Dominants
such as yellow paloverde are the first to reappear and replace
themselves following disturbance [69].
SEASONAL DEVELOPMENT :
Yellow paloverde may not flower every year, depending on adequate
moisture availability. It develops flowers from March to May
[24,31,80,91,100]. Leaf production is erratic [24]. Yellow paloverde
grows drought-deciduous leaves two or more times during the year
following summer and winter rains [77,91].
FIRE ECOLOGY
SPECIES: Cercidium microphyllum | Yellow Paloverde
FIRE ECOLOGY OR ADAPTATIONS :
The thin-barked photosynthetic stems of yellow paloverde are killed by
fire [13]. Yellow paloverde may sprout from the root crown following
top-kill [39].
The temperatures of desert fires are variable due to fluctuations in
kinds and quantities of available fuel [104]. Heavy grazing in some
upland sites has eliminated the grass understory beneath paloverde
species and saguaro. Grass species were replaced with bursage,
burroweed (Haplopappus tenuisectus), and snakeweed (Gutierrezia spp.).
This has lowered the fire frequency because there is insufficient fuel
to carry fires [70]. However, introduced annuals in other areas may
have increased both the frequency and the severity of fire [71,72].
Fires in the Sonoran Desert are generally infrequent and are low
severity due to low fuel loads [49]. However, fires can be relatively
common in the Sonoran Desert under appropriate conditions, especially
during the summer [39]. Two consecutive wet winters are probably needed
to develop fuel loads adequate to sustain fire. Fire is frequent in
desert grasslands on the eastern edge of the Sonoran Desert [49].
The Sonoran savanna grasslands are subtropical, fire-climax grasslands.
Most of these communities were destroyed through grazing and other land
management practices by the 1940's. Yellow paloverde grows in remnants
of these communities at their northern limits [8].
POSTFIRE REGENERATION STRATEGY :
Tree with adventitious-bud root crown/soboliferous species root sucker
Tall shrub, adventitious-bud root crown
Secondary colonizer - off-site seed
FIRE EFFECTS
SPECIES: Cercidium microphyllum | Yellow Paloverde
IMMEDIATE FIRE EFFECT ON PLANT :
Although entire yellow paloverde trees are rarely consumed during a
fire, they are top-killed or killed. Surviving yellow paloverde
rootstocks sprout following fire. Resprouting plants are susceptible to
death from repeated fires [39].
A fire on a southern Arizona rangeland during the 1900's burned for 2
days and killed paloverde species. Postfire recovery of the vegetation
was not mentioned in the article [29].
DISCUSSION AND QUALIFICATION OF FIRE EFFECT :
NO-ENTRY
PLANT RESPONSE TO FIRE :
During May 1981 in the Tonto National Forest, Arizona, the prefire mean
density of yellow paloverde was 30 plants per acre (75 plants/ha).
Following a controlled fire of moderate severity during June 1981,
yellow paloverde mean density was 24.8 plants per acre (62 plants/ha).
Heat-damaged plants subsequently died. Nine months after the fire,
yellow paloverde mean density was 17.2 plants per acre (43 plants/ha)
[13].
Yellow paloverde was completely eliminated by fire at one site on the
Tonto National Forest, Arizona [13].
Yellow paloverde may require 20 years to return to prefire plant
densities and community species composition following fires in
paloverde-saguaro communities [13,39,72].
Wildfire during June 1979 in Arizona top-killed 83 percent of yellow
paloverde present. Twenty-five percent of top-killed plants sprouted
about 2 years following the fire. There was 63 percent mortality for
yellow paloverde after about 3 years [49].
Fire burned during June 1974 in two desert scrub communities of
south-central Arizona. Before the fires, yellow paloverde had not
sprouted; no seedlings were present on one site (Dead Man Wash Site),
and five seedlings were present at the other site (Saguaro Site).
Prefire data concerning yellow paloverde were not given. Fire killed 78
percent of the photosynthetic tissue on the Dead Man Wash Site and 92
percent on the Saguaro Site. For both sites, approximately 10 percent
of the yellow paloverde present after fire were not top-killed;
approximately 14 percent were top-killed and resprouted. Five seedlings
were found on the Saguaro Site in postfire year 1 [71,72].
Yellow paloverde occurred in two different communities that were
prescribed burned during different years, one in 1983 and the other in
1985. Control and prefire communities were similar in composition. No
information specific to yellow paloverde was given. The fires consumed
70 percent of the perennial vegetation. Plants were two-thirds less
dense immediately after than before the fire. In 1986, plant densities
were still below prefire levels [39].
Yellow paloverde was codominant with triange bursage and buckhorn cholla
(Opuntia acanthocarpa) on rocky slopes on the Tonto National Forest. A
prescribed fire during June 1985 burned 9.9 acres (4 ha). The fire
burned vigorously in washes and on lower slopes. But fire decreased on
the upper slopes due to a lack of fuel between the shrubs; vegetation
patches were ignited with flares. The spotty burning reduced shrub
cover by 49 percent. No specific effects on yellow paloverde response
to fire were given in the article [81].
DISCUSSION AND QUALIFICATION OF PLANT RESPONSE :
NO-ENTRY
FIRE MANAGEMENT CONSIDERATIONS :
Introduced annuals in desert habitats may create sufficient fuel to
increase fire frequency and severity [71]. Native annuals probably
provided less fuel [39,71].
In the soils on which yellow paloverde occurs, nutrients are quickly
translocated following fire. Two years after fire, soil nitrogen levels
can drop below prefire levels [13,101].
FIRE CASE STUDIES
SPECIES: Cercidium microphyllum | Yellow Paloverde
CASE NAME :
Bulldog Canyon Prescribed Fire Study
SEASON/SEVERITY CLASSIFICATION :
summer fire/low-severity
STUDY LOCATION :
The study was located in Bulldog Canyon on the Tonto National Forest,
Arizona, at 33 degrees 15 minutes north latitude and 111 degrees 22
minutes west longitude.
PREFIRE VEGETATIVE COMMUNITY :
A yellow paloverde-saguaro (Cercidium microphyllum-Carnegiea gigantea)
community covered Bulldog Canyon. Standing dead biomass was assessed in
April before the fire. Three microhabitats were evaluated: (1) open
shrubless interspaces which covered 70 percent of the ground, (2) yellow
paloverde covered 8 percent, and (3) triangle bursage (Ambrosia
deltoidea) covered 15 percent.
Total perennial plant cover was measured prefire in April and
immediately postfire in June. Twenty-three 12x26 feet (4x8 m) random
quadrats were located along parallel transects systematically placed
every 32.8 feet (10 m) throughout the study area. Prefire mean total
perennial plant cover was 30.7 with a standard error of 3.4 percent.
TARGET SPECIES PHENOLOGICAL STATE :
Phenological stages of the plants were not specifically mentioned. At
the time of burning in June, yellow paloverde would be past flowering,
and fruits would be developing.
SITE DESCRIPTION :
The study site was located in a desert canyon at 1,477 feet (450 m)
elevation. Spring months are dry and warm in this semiarid climate. No
appreciable precipitation was reported from the April prefire
assessments to the June prescribed fire. No information was given on
specific topography, slope, or soils.
FIRE DESCRIPTION :
Plots were placed to assess prefire surface fuels such as dead litter
and annual plants. Twenty 7.9x7.9 inch (20x20 cm) plots were randomly
located in both the open and the triangle bursage microhabitats.
Thirty-two similar plots were located under eight yellow paloverde, one
at each of the four cardinal directions. Average fuels are given in the
following table:
microhabitat mean (standard error)g/sq m
open 69.9 ( 7.5)
triangle bursage 143.3 (32.6)
yellow paloverde 319.4 (56.5)
The fire burned 12 June 1981. Air temperatures ranged from 104 degrees
Fahrenheit (40 deg C) in the shade to 132.8 degrees Fahrenheit (50 deg
C) at 0.39 inch (1 cm) above an unshaded soil surface. The relative
humidity remained at 29 percent during the fire. Mean air movement
during the fire was low at 0.003 foot per second (0.001 m/sec) with
gusts up to 9 feet per second (2.75 m/sec). Mean soil moisture in the
top 2 inches (5 cm) of soil was 0.61 and 0.80 percent for open and
shaded areas, respectively, with standard errors less than 0.1 percent.
Maximum temperatures for each microhabitat were estimated with
temperature sensitive pellets placed 0.39 and 0.78 inch (1 and 2 cm)
below the soil surface and 0.39 and 11.8 inches (1 and 30 cm) above the
soil surface. Additional measurements were made with thermocouples at
0.39 inch (1 cm) below soil surface, at the soil surface, and 11.8
inches (30 cm) above the soil surface in the three microhabitats.
Temperatures were lowest in open microhabitats and highest in triangle
bursage areas (see table below). Temperatures beneath yellow paloverde
were intermediate. Fire had little influence on soil temperatures at
0.39 and 0.79 inch (1 and 2 cm) below the soil surface. Temperatures at
0.39 inch (1 cm) above the soil surface burned the hottest.
Temperatures 0.39 inch (1 cm) above soil surface were significantly
(P<0.05) higher from temperatures 0.79 inch (2 cm) below the soil
surface for yellow paloverde and triangle bursage microhabitats.
mean maximum temperatures (deg C) during fire*
(standard error in parentheses)
vertical microhabitat
location (cm) open yellow paloverde triangle bursage
30 76(76)ax 167(33)abx 210(54)abx
1 88(51)ax 299(17) bxy 405(16) b y
- 1 61( 5) x 63( 7) x 90( 9) x
- 2 60( 0)ax 57( 2)a x 60( 2)a x
*Means not significantly different (P<0.05) within each vertical location
are indicated by the same letter (a,b) and within microhabitats (x,y).
As fire moved through yellow paloverde microhabitats, it burned lightly
leaving some litter and duff unburned. Additionally, the thick litter
and duff beneath yellow paloverde insulated the soil from the fire.
The increase in soil surface albedo after the fire was not significant
(P=0.08). A small increase in water repellency was not expected to
create erosion or runoff problems.
FIRE EFFECTS ON TARGET SPECIES :
No fire effects information specific to yellow paloverde was given.
Fires were low severity and did not consume all litter and duff below
yellow paloverde. However, yellow paloverde has thin bark and
photosynthetic trunks that make it susceptible to top-kill by fire.
FIRE MANAGEMENT IMPLICATIONS :
Desert fire temperatures are variable due to interactions of
microhabitats and fuel. This prescribed fire did not alter physical
site characteristics such as albedo, soil water repellency, and
long-term microsite temperatures. Perennial plant cover was
significantly (P=0.001) reduced which may lead to soil erosion. Yellow
paloverde is very susceptible to fire, but no mortality data were given.
REFERENCES
SPECIES: Cercidium microphyllum | Yellow Paloverde
REFERENCES :
1. Asplund, Kenneth K.; Gooch, Michael T. 1988. Geomorphology and the
distributional ecology of Fremont cottonwood (Populus fremontii) in a
desert riparian canyon. Desert Plants. 9(1): 17-27. [563]
2. Bennett, Peter S.; Kunzmann, Michael R.; Johnson, R. Roy. 1989. Relative
nature of wetlands: riparian and vegetational considerations. In: Abell,
Dana L., technical coordinator. Protection, management, and restoration
for the 1990's: Proceedings of the California riparian systems
conference; 1988 September 22-24; Davis, CA. Gen. Tech. Rep. PSW-110.
Berkeley, CA: U.S. Department of Agriculture, Forest Service, Pacific
Southwest Forest and Range Experiment Station: 140-142. [13516]
3. Benson, Lyman; Darrow, Robert A. 1981. The trees and shrubs of the
Southwestern deserts. Tucson, AZ: The University of Arizona Press.
[18066]
4. 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]
5. Bowers, Michael A. 1988. Plant associations on a Sonoran Desert bajada:
geographical correlates and evolutionary source pools. Vegetatio. 74:
107-112. [4408]
6. Bowers, Michael A.; Lowe, Charles H. 1986. Plant-form gradients on
Sonoran Desert bajadas. Oikos. 46: 284-291. [10864]
7. Brooks, William H. 1978. Jojoba--a North American desert shrub; its
ecology, possible commercialization, & potential as an introd. into
other arid regions. Journal of Arid Environments. 1: 227-236. [5162]
8. Brown, David E. 1982. Sonoran savanna grassland. In: Brown, David E.,
ed. Biotic communities of the American Southwest--United States and
Mexico. Desert Plants. 4(1-4): 137-141. [8897]
9. Burgess, Tony L.; Bowers, Janice E.; Turner, Raymond M. 1991. Exotic
plants at the Desert Laboratory, Tucson, Arizona. Madrono. 38(2):
96-114. [15362]
10. Burk, Jack H. 1977. Sonoran Desert. In: Barbour, M. G.; Major, J., eds.
Terrestrial vegetation of California. New York: John Wiley and Sons:
869-899. [3731]
11. Carr, Merle E.; Mason, Charles T., Jr.; Bagby, Marvin O. 1986. Renewable
resources from Arizona trees and shrubs. Forest Ecology and Management.
16: 155-167. [3053]
12. Castellanos, A. E.; Molina, F. E. 1990. Differential survivorship and
establishment in Simmondsia chinensis (jojoba). Journal of Arid
Environments. 19: 65-76. [14982]
13. Cave, George Harold, III. 1982. Ecological effects of fire in the upper
Sonoran Desert. Tempe, AZ: Arizona State University. 124 p. Thesis.
[12295]
14. Ciesla, Bill. 1993. Cactus condo. American Forests. 99(5&6): 25-28, 58.
[20995]
15. Eddy, Thomas A. 1961. Foods and feeding patterns of the collared peccary
in southern Arizona. Journal of Wildlife Management. 25: 248-257.
[9888]
16. Elias, Thomas S. 1980. The complete trees of North America: field guide
and natural history. New York: Times Mirror Magazines, Inc. 948 p.
[21987]
17. Eyre, F. H., ed. 1980. Forest cover types of the United States and
Canada. Washington, DC: Society of American Foresters. 148 p. [905]
18. Felker, Peter; Cannell, G. H.; Clark, Peter R.; [and others]. 1983.
Biomass production of Prosopis species (mesquite), Leucaena, and other
leguminous trees grown under heat/drought stress. Forest Science. 29(3):
592-606. [4765]
19. Fernandes, G. Wilson. 1992. A gradient analysis of plant forms from
northern Arizona. Journal of the Arizona-Nevada Academy of Science.
24-25: 21-30. [18247]
20. Franco, A. C.; Nobel, P. S. 1989. Effect of nurse plants on the
microhabit and growth of cacti. Journal of Ecology. 77: 870-886. [9766]
21. 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]
22. Goldberg, Deborah E.; Turner, Raymond M. 1986. Vegetation change and
plant demography in permanent plots in the Sonoran Desert. Ecology.
67(3): 695-712. [4410]
23. Goodwin, John G., Jr.; Hungerford, C. Roger. 1977. Habitat use by native
Gambel's and scaled quail and released masked bobwhite quail in southern
Arizona. Res. Pap. RM-197. Fort Collins, CO: U.S. Department of
Agriculture, Forest Service, Rocky Mountain Forest and Range Experiment
Station. 8 p. [14970]
24. Hanley, Thomas A.; Brady, Ward W. 1977. Seasonal fluctuations in
nutrient content of feral burro forages, lower Colorado River Valley,
Arizona. Journal of Range Management. 30(5): 370-375. [4336]
25. Hanley, Thomas A.; Brady, Ward W. 1977. Feral burro impact on a Sonoran
Desert range. Journal of Range Management. 30(5): 374-377. [4337]
26. Hastings, James R.; Turner, Raymond M.; Warren, Douglas K. 1972. An
atlas of some plant distributions in the Sonoran Desert. Technical
Reports on the Meteorology and Climatology of Arid Regions No. 21.
Tuscon, AZ: University of Arizona, Institute of Atmospheric Physics. 255
p. [10534]
27. Holland, Robert F. 1986. Preliminary descriptions of the terrestrial
natural communities of California. Sacramento, CA: California Department
of Fish and Game. 156 p. [12756]
28. Humphrey, R. R. 1950. Arizona range resources. II. Yavapai County. Bull.
229. Tucson, AZ: University of Arizona, Agricultural Experiment Station.
55 p. [5088]
29. Humphrey, Robert R. 1958. The desert grassland: A history of
vegetational change and an analysis of causes. Bull. 299. Tucson, AZ:
University of Arizona, Agricultural Experiment Station. 61 p. [5270]
30. Hutto, Richard L.; McAuliffe, Joseph R.; Hogan, Lynee. 1986.
Distributional associates of the saguaro (Carnegiea gigantea).
Southwestern Naturalist. 31(4): 469-476. [1229]
31. Kearney, Thomas H.; Peebles, Robert H.; Howell, John Thomas; McClintock,
Elizabeth. 1960. Arizona flora. 2d ed. Berkeley, CA: University of
California Press. 1085 p. [6563]
32. Kennedy, Charles E. 1983. A palo verde snag in the Sonora Desert. In:
Davis, Jerry W.; Goodwin, Gregory A.; Ockenfeis, Richard A., technical
coordinators. Snag habitat management: proceedings of the symposium;
1983 June 7-9; Flagstaff, AZ. Gen. Tech. Rep. RM-99. Fort Collins, CO:
U.S. Department of Agriculture, Forest Service, Rocky Mountain Forest
and Range Experiment Station: 165-166. [17832]
33. Kingsolver, J. M.; Johnson, C. D.; Swier, S. R.; Teran, A. 1977.
Prosopis fruits as a resource for invertebrates. In: Simpson, B. B., ed.
Mesquite: Its biology in two desert ecosystems. US/IBP Synthesis 4.
Stroudsburg, PA: Dowden, Hutchinson & Ross, Inc: 108-122. [5193]
34. Krausman, Paul R.; Ordway, Leonard L.; Whiting, Frank M.; Brown, William
H. 1990. Nutritional compostition of desert mule deer forage in the
Picacho Mountains, Arizona. Desert Plants. 10(1): 32-34. [7259]
35. 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]
36. Leitner, Lawrence A. 1987. Plant communities of a large arroyo at Punta
Cirio, Sonora. Southwestern Naturalist. 32(1): 21-28. [1439]
37. Little, Elbert L., Jr. 1950. Southwestern trees: A guide to the native
species of New Mexico and Arizona. Agriculture Handbook No. 9.
Washington, DC: U.S. Department of Agriculture, Forest Service. 109 p.
[20330]
38. Little, Elbert L., Jr. 1976. Atlas of United States trees. Volume 3.
Minor western hardwoods. Misc. Publ. 1314. Washington, DC: U.S.
Department of Agriculture, Forest Service. 13 p. 290 maps. [10430]
39. Loftin, Samuel Robert. 1987. Postfire dynamics of a Sonoran Desert
ecosystem. Tempe, AZ: Arizona State University. 97 p. Thesis. [12296]
40. Loope, Lloyd L.; Sanchez, Peter G.; Tarr, Peter W.; [and others]. 1988.
Biological invasions of arid land nature reserves. Biological
Conservation. 44: 95-118. [3263]
41. Lowe, Charles H., Jr. 1961. Biotic communities in the sub-Mogollon
region of the inland Southwest. Arizona Academy of Science Journal. 2:
40-49. [20379]
42. Lowe, Charles H.; Holm, Peter A. 1991. The amphibians and reptiles at
Saguaro National Monument, Arizona. Technical Report No. 37. Tucson, AZ:
University of Arizona, School of Renewable Natural Resources,
Cooperative National Park Resources Study Unit. 20 p. [18335]
43. MacMahon, James A. 1988. Warm deserts. In: Barbour, Michael G.;
Billings, William Dwight, eds. North American terrestrial vegetation.
Cambridge; New York: Cambridge University Press: 231-264. [19547]
44. McArthur, E. Durant. 1989. Breeding systems in shrubs. In: McKell, Cyrus
M., ed. The biology and utilization of shrubs. San Diego, CA: Academic
Press, Inc.: 341-361. [8039]
45. McAuliffe, Joseph R. 1986. Herbivore-limited establishment of a Sonoran
Desert tree, Cercidium microphyllum. Ecology. 67(1): 276-280. [2756]
46. McAuliffe, Joseph R. 1988. Markovian dynamics of simple and complex
desert plant communities. American Naturalist. 131(4): 459-490. [6744]
47. McAuliffe, Joseph R. 1990. Paloverdes, pocket mice, and bruchid beetles:
interrelationships of seeds, dispersers, and seed predators.
Southwestern Naturalist. 35(3): 329-337. [14988]
48. McGinnies, W. G.; Arnold, Joseph F. 1939. Relative water requirement of
Arizona range plants. Technical Bulletin No. 80. Tucson, AZ: University
of Arizona, Agricultural Experiment Station: 167-246. [4441]
49. McLaughlin, Steven P.; Bowers, Janice E. 1982. Effects of wildfire on a
Sonoran Desert plant community. Ecology. 63(1): 246-248. [1619]
50. Minckley, W. L.; Clark, Thomas O. 1981. Vegetation of the Gila River
Resource Area, eastern Arizona. Desert Plants. 3(3): 124-140. [10863]
51. Moir, W. H. 1983. A series vegetation classification for Region 3. In:
Moir, W. H.; Hendzel, Leonard, tech. coords. Proceedings of the workshop
on Southwestern habitat types; 1983 April 6-8; Albuquerque, NM.
Albuquerque, NM: U.S. Department of Agriculture, Forest Service,
Southwestern Region: 91-95. [1672]
52. Munz, Philip A. 1974. A flora of southern California. Berkeley, CA:
University of California Press. 1086 p. [4924]
53. Nichol, A. A. [revisions by Phillips, W. S.]. 1952. The natural
vegetation of Arizona. Tech. Bull. 68 [revision]. Tucson, AZ: University
of Arizona, Agricultural Experiment Station: 189-230. [3928]
54. Niering, William A.; Lowe, Charles H. 1984. Vegetation of the Santa
Catalina Mountains: community types and dynamics. Vegetatio. 58: 3-28.
[12037]
55. Niering, W. A.; Whittaker, R. H.; Lowe, C. H. 1963. The saguaro: a
population in relation to environment. Science. 142(3588): 15-23.
[5093]
56. Norem, M. A.; Day, A. D.; Ludeke, K. L. 1982. An evaluation of shrub and
tree species used for revegetating copper mine wastes in the
south-western United States. Journal of Arid Environments. 5: 99-304.
[1776]
57. Olsen, Ronald W. 1973. Shelter-site selection in the white-throated
woodrat, Neotoma albigula. Journal of Mammalogy. 54: 594-610. [9886]
58. Parker, Kathleen C. 1986. Partitioning of foraging space and nest sites
in a desert shrubland bird community. American Midland Naturalist.
115(2): 255-267. [19258]
59. Parker, Kathleen C. 1988. Environmental relationships and vegetation
associates of columnar cacti in the northern Sonoran Desert. Vegetatio.
78: 125-140. [6953]
60. Parker, Kathleen C. 1991. Topography, substrate, and vegetation patterns
in the northern Sonoran Desert. Journal of Biogeography. 18: 151-163.
[14979]
61. 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]
62. Raunkiaer, C. 1934. The life forms of plants and statistical plant
geography. Oxford: Clarendon Press. 632 p. [2843]
63. Rautenstrauch, Kurt R.; Krausman, Paul R.; Whiting, Frank M.; Brown,
William H. 1988. Nutritional quality of desert mule deer forage in King
Valley, Arizona. Desert Plants. 8(4): 172-174. [2768]
64. Rea, Amadeo. 1979. Velvet mesquite. Environment Southwest. 486: 3-7.
[2977]
65. Rea, Amadeo M. 1983. Sonoran desert oases: plants, birds and native
people. Environment Southwest. 503: 5-9. [2967]
66. Rea, Amadeo M. 1991. Gila River Pima dietary reconstruction. Arid Lands
Newsletter. 31: 3-10. [18255]
67. Reichman, O. J. 1975. Relation of desert rodent diets to available
resources. Journal of Mammalogy. 56(4): 731-751. [4572]
68. Reichman, O. J. 1976. Relationships between dimensions, weights,
volumes, and calories of some Sonoran Desert seeds. Southwestern
Naturalist. 20(4): 573-574. [12326]
69. Reynolds, Hudson G. 1962. Some characteristics and uses of Arizona's
major plant communities. Journal of the Arizona Academy of Science. 2:
62-71. [1959]
70. Robinett, Dan. 1990. Tohono O'odham range history. Rangelands. 12(6):
296-300. [14968]
71. Thomas, Renee L.; Anderson, Roger C. 1993. Influence of topography on
stand composition in a midwestern ravine forest. American Midland
Naturalist. 130(1): 1-12. [1742]
72. Rogers, Garry F.; Steele, Jeff. 1980. Sonoran Desert fire ecology. In:
Stokes, Marvin A.; Dieterich, John H., technical coordinators.
Proceedings of the fire history workshop; 1980 October 20-24; Tucson,
AZ. Gen. Tech. Rep. RM-81. Fort Collins, CO: U.S. Department of
Agriculture, Forest Service, Rocky Mountain Forest and Range Experiment
Station: 15-19. [16036]
73. Roundy, Bruce A.; Dobrenz, Albert K. 1989. Herbivory and plant water
status of jojoba [Simmondsia chinensis (Link) Schn.] in the Sonoran
Desert in Arizona. Journal of Arid Environments. 16: 283-291. [7865]
74. Rucks, Michael G. 1984. Composition and trend of riparian vegetation on
five perennial streams in southeastern Arizona. In: Warner, Richard E.;
Hendrix, Kathleen M., eds. California riparian systems: Ecology,
conservation, and productive management: Proceedings of a conference;
1981 September 17-19; Davis, CA. Berkeley, CA: University of California
Press: 97-107. [5831]
75. Scarbrough, David L.; Krausman, Paul R. 1988. Sexual segregation by
desert mule deer. Southwestern Naturalist. 33(2): 157-165. [5250]
76. Seegmiller, Rick F.; Krausman, Paul R.; Brown, William H.; Whiting,
Frank M. 1990. Nutritional composition of desert bighorn sheep forage in
the Harquahala Mountains, Arizona. Desert Plants. 10(2): 87-90. [11943]
77. Shreve, Forrest. 1911. Establishment behavior of the Palo Verde. Plant
World. 14: 289-296. [11168]
78. Shreve, Forrest. 1942. The desert vegetation of North America. Botanical
Review. 8(4): 195-246. [5051]
79. Shreve, Forrest; Hinckley, Arthur L. 1937. Thirty years of change in
desert vegetation. Ecology. 18(4): 463-478. [4574]
80. Shreve, F.; Wiggins, I. L. 1964. Vegetation and flora of the Sonoran
Desert. Stanford, CA: Stanford University Press. 2 vols. [21016]
81. Simons, L. H. 1989. Vertebrates killed by desert fire. Southwestern
Naturalist. 34(1): 144. [7850]
82. Simpson, B. B.; Neff, J. L.; Moldenke, A. R. 1977. Prosopis flowers as a
resource. In: Simpson, B. B., ed. Mesquite: Its biology in two desert
ecosystems. US/IBP Synthesis 4. Stroudsburg, PA: Dowden, Hutchinson &
Ross, Inc: 84-107. [5192]
83. Stamp, Nancy E. 1978. Breeding birds of riparian woodland in
south-central Arizona. Condor. 80: 64-71. [8079]
84. Steenbergh, Warren F.; Lowe, Charles H. 1969. Critical factors during
the first years of the saguaro (Cereus giganteus) at Saguaro National
Monument, Arizona. Ecology. 50(5): 825-834. [19692]
85. 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]
86. Szaro, Robert C.; Belfit, Scott C. 1987. Small mammal use of a desert
riparian island and its adjacent scrub habitat. Res. Note RM-473. Fort
Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky
Mountain Forest and Range Experiment Station. 5 p. [3843]
87. Thornber, J. J. 1910. The grazing ranges of Arizona. Bull. No. 65.
Tucson, AZ: University of Arizona, Agricultural Experiment Station. 360
p. [4555]
88. Tidestrom, I.; Kittell, T. 1941. A flora of Arizona and New Mexico.
Washington, DC: The Catholic University of America Press. 897 p.
[18145]
89. Tomoff, Carl S. 1974. Avian species diversity in desert scrub. Ecology.
55: 396-403. [19307]
90. Turnage, William V.; Hinckley, Arthur L. 1938. Freezing weather in
relation to plant distribution in the Sonoran Desert. Ecological
Monographs. 8(2): 530-550. [3789]
91. Turner, Raymond M. 1963. Growth in four species of Sonoran Desert trees.
Ecology. 44: 760-765. [9883]
92. Turner, Raymond M. 1990. Long-term vegetation change at a fully
protected Sonoran Desert site. Ecology. 7(2): 464-477. [10866]
93. Turner, Raymond M.; Brown, David E. 1982. Sonoran desertscrub. In:
Brown, David E., ed. Biotic communities of the American
Southwest--United States and Mexico. Desert Plants. 4(1-4): 181-221.
[2375]
94. 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]
95. Vander Wall, Stephen B. 1993. Seed water content and the vulnerability
of buried seeds to foraging rodents. American Midland Naturalist.
129(2): 272-281. [21306]
96. Vorhies, Charles T.; Taylor, Walter P. 1933. The life histories and
ecology of jack rabbits, Lepus alleni and Lepus californicus ssp., in
relation to grazing in Arizona. Technical Bulletin No. 49. Tucson, AZ:
University of Arizona, Agricultural Experiment Station. 117 p. [9933]
97. Warren, Peter L.; Anderson, L. Susan. 1985. Gradient analysis of a
Sonoran Desert wash. In: Johnson, R. Roy; [and others], technical
coordinators. Riparian ecosystems & their mgmt: reconciling conflicting
issues: Proceedings, 1st North American riparian conference; 1985 April
16-18; Tucson, AZ. Gen. Tech. Rep. RM-120. Fort Collins, CO: U.S.
Department of Agriculture, Forest Service, Rocky Mountain Forest and
Range Experiment Station: 150-155. [17158]
98. Whitfield, Charles J.; Anderson, Hugh L. 1938. Secondary succession in
the desert plains grassland. Ecology. 19(2): 171-180. [5252]
99. Whittaker, R. H.; Niering, W. A. 1965. Vegetation of the Santa Catalina
Mountains, Arizona: a gradient analysis of the south slope. Ecology. 46:
429-452. [9637]
100. Wiggins, Ira L. 1980. Flora of Baja California. Stanford, CA: Stanford
University Press. 1025 p. [21993]
101. Whysong, Gary L.; Heisler, Michael H. 1978. Nitrogen levels of soil and
vegetation in the upper Sonoran Desert as affected by fire. In: Hyder,
Donald N., ed. Proceedings, 1st international rangeland congress; 1978
August 14-18; Denver, CO. Denver, CO: Society for Range Management:
697-699. [3990]
102. Yang, Tien Wei; Lowe, Charles H., Jr. 1955. Correlation of major
vegetation climaxes with soil characteristics in the Sonoran Desert.
Science. 123: 542. [12226]
103. Zimmermann, Robert C. 1969. Plant ecology of an arid basin: Tres
Alamos-Redington Area, southeastern Arizona. Geological Survey
Professional Paper 485-D. Washington, DC: U.S. Department of the
Interior, Geological Survey. 51 p. [4287]
104. Patten, Duncan T.; Cave, George H. 1984. Fire temperatures and physical
characteristics of a controlled burn in the upper Sonoran Desert.
Journal of Range Management. 37(3): 277-280. [181]
105. Shreve, Forrest. 1917. The establishment of desert perennials. Journal
of Ecology. 5: 210-216. [22785]
Index
Related categories for Species: Cercidium microphyllum
| Yellow Paloverde
|
|