MESA VERDE
Environment of Mesa Verde, Colorado
Wetherill Mesa Studies
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Chapter 3
description of the stands
LOWEST MESA-TOP SITE, M1
This site was near the south end of Chapin Mesa,
about 5 miles from park headquarters (fig. 1). The lowest of the
mesa-top sites, at 6,650-foot elevation, M1 was on a broad, level
ridgetop flanked by two shallow washes that empty into the 1,000-foot
deep Mancos River canyon about 1/4 mile away.
The vegetation is a juniper-pinyon/bitterbrush
woodland with sparse herbs (fig. 4). Ephemeral spring flowers are important
in the ground cover. All species observed in the stand are listed in
table 2; quantitative data on trees are given in table 3. Ten of the
largest trees were 300 to 400 years old, with the oldest pith date being
A.D. 1529. The trees are small and widely spaced, and bitterbrush
(Purshia tridentata) and black sagebrush (Artemisia nova)
are common in openings between them. Herbs are conspicuous only
during the spring and early summer growing season. Some of the most
common ones are mutton grass (Poa fendleriana), vetch
(Astragalus wingatanus), and phlox (Phlox hoodii).
TABLE 2.LIST OF SPECIES OBSERVED IN THE ENVIRONMENT MEASUREMENT SITES
Species | Sites |
Mesa top | Canyon |
M1 | M2 | M3 |
C1 | C2 | C3 |
TREE LAYER |
|
Juniperus osteosperma (Torr.) Little | 1X | X | X | X | X | X |
Juniperus scoputorum Sarg |
|
| X |
|
|
|
Pinus edulis Engelm | X | X | X | X | X | X |
Pseudotsuga menziesii (Mirb.) Franco |
|
| X |
|
|
|
SHRUB LAYER |
|
Amelanchier utahensis Koehne |
|
| X | X |
| X |
Artemisia nova A. Nels | X |
| X |
|
|
|
Artemisia tridentata Nutt |
|
|
| X | X | X |
Atriplex canescens (Pursh) Nutt |
|
|
| X | X |
|
Cercocarpus montanus Raf |
|
| X | X |
| X |
Chrysothamnus depressus Nutt | X |
| X |
|
|
|
Chrysothamnus nauseosus (Pall.) Britt |
|
|
| X | X |
|
Chrysothamnus viscidiflorus (Hook.) Nutt |
|
| X |
|
|
|
Ephedra viridis Coville | X |
|
| X |
| X |
Fendlera rupicola A. Gray |
|
| X |
|
| X |
Gutierrezia sarothrae (Pursh) Britt. & Rusby | X |
|
| X | X | X |
Philadelphus microphyllus A. Gray |
|
|
|
|
| X |
Purshia tridentata (Pursh) DC | X |
|
| X |
|
|
Quercus gambelii Nutt |
|
| 2X° |
| X | X |
Rhus trilobata Nutt. ex T. & G |
|
| X |
| X |
|
Ribes leptanthum A. Gray |
|
|
|
| X |
|
Stanleya pinnata (Pursh) Britt |
|
|
| X |
|
|
Symphoricarpos oreophilus A. Gray |
|
| X° | X | X | X |
Tetradymia canescens DC |
|
| X |
|
|
|
Yucca baccata Torr | X | X | X |
| X | X |
GRASS AND FORB LAYER |
|
Agropyron smitthii Rydb |
|
|
| X | X | X |
Bouteloua gracilis (H. B. K.) Lag |
|
|
|
| X |
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Bromus tectorum L |
|
|
| X | X | X |
Hilaria jamesii (Torr.) Benth |
|
|
| X |
|
|
Koeleria gracilis Pers |
|
| X |
| X |
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Oryzopsis micrantha (Trin. & Rupr.) Thurb |
|
|
|
| X |
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Poa agassizensis Boivin & D. Love |
|
|
|
| X |
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Poa fendleriana (Steud.) Vasey | X | X | X | X | X | X |
Sitanion longifolium J. G. Smith | X |
| X° | X | X | X |
Stipa comata Trin. & Rupr |
|
| X |
|
|
|
Achillea lanulosa Nutt |
|
| X° |
| X |
|
Amaranthus hybridus L |
|
|
|
| X |
|
Androsace septentrionalis L |
|
|
|
| X | X |
Antennaria dimorpha (Nutt.) T. & G |
|
| X |
|
|
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Antennaria parvifolia Nutt |
|
|
|
|
| X |
Arabis drummondii A. Gray |
|
| X |
|
|
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Arabis pulchra M. E. Jones ex S. Wats | X |
|
|
|
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Arabis selbyi Rydb | X | X | X | X |
| X |
Arenaria congesta Nutt. ex T. & G |
|
|
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Artemisia ludoviciana Nutt |
|
| X° | X | X | X |
Aster arenosus Blake |
|
|
| X |
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Astragalus calycosus Torr. ex S. Wats | X |
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Astragalus flexuosus Dougl. ex Hook |
|
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| X | X |
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Astragalus lentiginosus Dougl |
|
|
| X |
|
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Astragalus schmollae C. L. Porter |
| X |
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Astragalus scopulorum T. C. Porter |
| X | X |
|
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Astragalus wingatanus S. Wats | X |
|
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Balsamorhiza sagittata (Pursh) Nutt |
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| X |
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Calochortus nuttallii Torr | X |
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Castilleja chromosa A. Nels |
| X | X |
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Castilleja linariaefolia Benth. in DC |
|
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| X |
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Chaenactis douglasii (Hook.) H. & A |
|
|
| X |
| X |
Chenopodium fremontii S. Wats |
| X |
| X |
| X |
Claytonia lanceolata Pursh |
|
| X° |
|
|
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Comandra umbellata (L.) Nutt |
|
| X |
|
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Crepis cf. occidentalis Nutt |
|
| X |
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Cryptantha bakeri (Greene) Payson | X |
|
| X |
| X |
Cryptantha gracilis Osterhout | X |
|
|
|
| X |
Cymopterus bulbosus A. Nels |
|
| X |
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Cymopterus purpurascens (A. Gray) M. E. Jones |
|
|
|
|
| X |
Cymopterus purpureus S. Wats | X |
|
| X |
|
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Delphinium nelsonii Greene |
|
| X° |
|
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Descurainia pinnata (Walt.) Britt | X |
|
|
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Draba reptans (Lam.) Fern | X |
|
|
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| X |
Echinocereus coccineus Engelm |
|
|
| X |
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Erigeron divergens T. & G |
|
|
|
|
| X |
Erigeron flagellaris A. Gray |
|
| X |
|
| X |
Erigeron pumilus Nutt. |
|
| X |
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Erigeron speciosus (Lindl.) DC |
|
| X° |
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Eriogonum aatum Torr | X |
|
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Eriogonum jamesii Benth |
|
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| X | X |
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Eriogonum racemosum Nutt. |
| X | X |
|
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Eriogonum umbellatum Torr |
| X | X | X |
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Euphorbia fendleri T. & G | X |
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Frasera albomarginata S. Wats | X |
|
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Fritillaria atropurpurea Nutt |
|
| X |
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Galium coloradoense W. F. Wright |
|
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| X |
| X |
Gilia ophthalmoides Brand |
|
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| X |
Haplopappus armerioides (Nutt.) A. Gray | X |
|
| X |
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Haplopappus nuttallii T. & G | X |
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Hymenopappus filifolius Hook | X |
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Hymenoxys acaulis (Pursh) Parker | X |
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Impomopsis aggregata (Pursh) V. Grant |
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| X |
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Lappula redowskii (Hornem.) Greene |
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| X |
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Lathyrus pauciflorus Fern |
|
| X° |
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Lepidium montanum Nutt |
|
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| X | X | X |
Lesquerella rectipes Woot. & Standl | X |
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Lithospermum incisum Lehm |
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| X |
Lithospermum ruderale Dougl. in Lehm |
|
| X |
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Lomatium dissectum (Nutt.) Math. & Const |
|
| X° |
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Lomatium grayi Coult. & Rose |
|
| X |
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Lomatium simplex (Nutt.) Macbr |
|
| X |
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Lupinus caudatus Kellogg |
| X | X |
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Machoeranthera bigelovii (A. Gray) Greene |
|
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| X | X |
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Mammillaria vivipara (Nutt.) Haw | X |
|
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Melilotus officinalis (L.) Lam |
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| X |
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Mertensiafusiformis Greene |
|
| X° |
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Microsteris humilis (Dougl.) Greene |
|
|
|
| X | X |
Mirabilia multiflora (Torr.) A. Gray |
|
|
|
|
| X |
Moldavica parviflora (Nutt.) Britt. |
|
|
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| X |
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Oenothera caespitosa Nutt |
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| X |
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Opuntia phaeacantha Engelm. ex Gray |
|
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| X |
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Opuntia polyacantha Haw | X | X |
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| X | X |
Pedicularis cent ranthera A. Gray | X | X |
|
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| X |
Penstemon bridgesii A. Gray |
|
|
| X |
| X |
Penstemon eatonii A. Gray |
|
|
| X |
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Penstemon linarioides A. Gray |
| X |
| X |
| X |
Penstemon strictus Benth | X |
| X° |
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Petrodoria pumila (Nutt.) Greene | X |
| X |
|
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Phacelia heterophylla Pursh |
|
| X° |
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Phlox hoodii Richardson | X |
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| X | X | X |
Phlox longifolia Nutt | X |
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| X | X |
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Physaria australis (Payson) Rollins | X |
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Polygonum sawatchense Small |
| X |
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Portulaca oleracea L |
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| X |
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Sclerocactus whipplei (Engelm. & Bigel.) Britt & Rose. | X |
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Senecia multilobatus T. & G. ex A. Gray | X |
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| X | X | X |
Sisymbrium linifolium Nutt |
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| X | X |
Solidago sparsiflora A. Gray |
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| X |
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Sphaeralcea coccinea (Pursh) Rydb |
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| X |
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Sphaeralcea parvifolia A. Nels |
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| X |
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Streptanthus cordatus Nutt. ex T. & G | X |
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| X |
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Taraxacum laevigatum (Willd.) DC |
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| X |
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Townsendia incana Nutt | X |
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Zygadenus venenosus S. Wats |
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| X |
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1Boldface X indicates species dominant within the
stand.
2X° indicates species occurs in both the oak thickets
and the sagebrush openings at M3; those restricted to the
thickets are Quercus gambelii, Lathyrus pauciflorus, Ligusticum
perteri, and Pacelia hterophylla.
TABLE 3.TREE DATA AT M1
A. Point quarter analysis based on 10 points |
Species |
Number of trees |
Average distance, feet |
Total basal area, square inches |
Average B.A./ diameter |
Density trees/acre |
Relative |
Importance value |
Density (%) |
Frequency (%) |
Dominance (%) |
Pinus edulis |
22 | -- | 645 | 29/6 |
156 | 55 | 50 | 30.2 | 135.2 |
Juniperus osteosperma |
18 | -- | 1,493 | 83/10.5 |
127 | 45 | 50 | 69.8 | 164.8 |
Total |
40 | 12.4 | 2,138 | 54/8 |
283 | 100 | 100 | 100.0 | 300.0 |
B. Pinyon-juniper reproduction based on number of individuals that
occurred within ten 4 x 50-foot belt transects |
Species |
Number of |
Total |
|
Seedlings | Saplings | Trees |
Pinus edulis | 24 | 22 | 10 | 56 |
Juniperus osteosperma | 12 | 3 | 11 | 26 |
The soils at the lower elevations of Mesa Verde are
generally high in calcium carbonate, due in part to the nature of the
underlying sandstone and in part to low rainfall and high temperatures.
Even though soils are relatively shallow in the M1 area, the
ground surface is free of rock material. According to Parsons, the soils
at this site are quite variable in depth as well as texture, but the
dominant type has been classified as Penrose channery loam. Montvale
fine sandy loam also occurs in small amounts. The soil profile in table
4 is typical of the M1 soils.
TABLE 4.SOIL PROFILE UNDERLYING THE M1 JUNIPER-PINYON/BITTERBUSH STAND*
Horizon | Depth, inches |
Description |
A1 | 03 |
Brown (10YR 5/3 dry) to dark brown (10YR 3/3 moist) channery loam; weak
fine platy structure, breaking to moderate very fine granular;
consistence soft dry and friable moist; many fine roots and pores; about
20 percent sandstone and shale channery; strongly calcareous; lower
boundary clear and smooth. |
Cca1 | 36 |
Pale brown (10YR 6/3 dry) to dark brown (10YR 4/3 moist) channery loam;
moderate fine granular structure; consistence slightly hard dry and
friable moist; many fine roots and root casts; approximately 25 percent
sandstone and shale channery; some small chalky concretions; violently
calcareous; lower boundary gradual and wavy. |
Cca2 | 611 |
Light yellowish brown (2.5Y 7/3 dry) to brown (2.5Y
5/3 moist) channery loam; weak coarse subangular blocky structure;
consistence hard dry and firm moist; some what sticky and plastic when
wet; 33 percent sandstone and shale channery; a few very fine patchy
clay skins show on rock surfaces; few small chalky concretions and
cicada casts; violently calcareous; lower boundary clear and smooth. |
C | 1117 |
Very pale brown (10YR 7/3 dry) to brown (10YR 5/3
moist) light clay loam; massive structure; slightly hard dry and firm
moist; slightly sticky wet; fine roots somewhat matted between sandstone
fragments; approximately 50 percent sandstone and shale channery;
strongly calcareous; lower boundary clear and smooth. |
R | 17+ |
Interbedded sandstone and shale with numerous tongues
of overlying horizon extending into cracks in rock. |
*Soil classified as Penrose channery loam.
The fine texture of the soil plays an important role
in the relationship of soil moisture to the growth of the plant
community. As shown in table 5, the storage capacity of growth-water in
the heavy soils at M1 is relatively high, especially when compared
to that of the soils at most of the other sites.
TABLE 5.SOIL MOISTURE CONSTANTS IN PERCENT DRY WEIGHT*
Moisture constant |
Depth, inches |
Sites |
M1 | M2 | M3 |
C1 | C2 | C3 |
Field capacity | 2 6 12 | 15.0 19.6 20.4 | 12.5 20.0 16.7 |
12.1 14.0 -- | 17.2 18.6 -- | 7.5 5.6 5.7 | 9.1 11.4 -- |
Permanent wilting percent | 2 6 12 | 8.l 11.6 12.4 | 7.1 10.6 9.3 |
7.2 8.9 -- | 17.2 18.6 -- | 4.3 3.1 3.5 | 5.0 6.3 -- |
Storage capacity of growth-water | 2 6 12 | 7.0 7.9 8.0 | 5.5 9.5 7.4 |
4.9 5.2 -- | 7.1 8.5 -- | 3.2 2.5 2.2 | 4.1 5.1 -- |
*Based on triplicate samples and determined by the moisture tension
method.
Once the soil dries out, however, and this occurs
quite early in the year, a large amount of water is required to moisten
the ground to the depth where roots are located. Moreover, because of
the sparse vegetational cover, even a light rain will induce splash
erosion of the surface particles, causing the pore spaces to clog and
subsequent rainfall to be largely lost as runoff. Thus, in the coarse to
fine loamy soils found at M1, only a small amount of the
precipitation percolates into the ground; this is especially true during
the summer, when rainfall is heavy. This phenomenon is shown graphically
in figure 15 (see ch. 4). The autumn frontal storms of 1962 wet the soil
down to the 12-inch level, whereas the 1963 summer thunderstorms were
not so effective.
Data for the atmospheric and soil factors are
presented in the appendix. Some of the features commonly used by
ecologists to characterize environments are given in table 6.
TABLE 6.SOME CLIMATIC FACTORS OF THE MESA-TOP SITES
Factor |
1962 | 1963 |
M1 | M2 | M3 |
M1 | M2 | M3 |
Air temperature (in degrees Farenheit): |
January: |
Maximum | 46 | 52 | 50 | 44 | 44 | 44 |
Mean maximum | 37 | 38 | 31 | 34 | 32 | 30 |
Minimum | -2 | -11 | -5 | -23 | -26 | -20 |
Mean minimum | 13 | 13 | 16 | 11 | 8 | 15 |
Mean | 25 | 26 | 24 | 22 | 20 | 23 |
July: |
Maximum | 97 | 91 | 84 | 97 | 93 | 86 |
Mean maximum | 89 | 84 | 77 | 91 | 86 | 79 |
Minimum | 46 | 48 | 47 | 52 | 50 | 50 |
Mean minimum | 56 | 54 | 55 | 59 | 56 | 58 |
Mean | 73 | 69 | 66 | 75 | 71 | 68 |
Annual: |
Maximum | 98 | 94 | 88 | 97 | 93 | 86 |
Month | Aug. | Aug. | Aug. | July | July | July |
Mean maximum | 64 | 62 | 54 | 64 | 61 | 55 |
Minimum | -3 | -11 | -5 | -23 | -26 | -20 |
Month | Feb. | Jan. | Jan. | Jan. | Jan. | Jan. |
Mean minimum | 36 | 35 | 36 | 37 | 34 | 37 |
Mean | 50 | 49 | 45 | 50 | 48 | 46 |
Frost-free period, days | 166 | 161 | 162 | 171 | 171 | 171 |
Last freeze in spring | 22 May | 28 May | 28 May | 12 May | 12 May | 12 May |
First freeze in autumn | 5 Nov. | 6 Nov. | 7 Nov. | 31 Oct. | 31 Oct. | 31 Oct. |
Relative humidity (in percentage): |
Lowest | 1 | 5 | 9 | 4 | 8 | 13 |
Month | May | May | May | Apr. | May | Nov. |
Lowest monthly mean | 22 | 36 | 35 | 29 | 33 | 36 |
Month | June | June | June | May | May | May |
Annual mean | 43 | 53 | 51 | 50 | 52 | 54 |
Precipitation (inches): |
Monthly total: |
Highest | 2.38 | 2.74 | 2.94 | 3.96 | 4.54 | 7.62 |
Month | Oct. | Oct. | Oct. | Aug. | Aug. | Aug. |
Lowest | 0.09 | 0.20 | 0.39 | 0.02 | 0.07 | 0.07 |
Month | June | June | Apr. | June | June | June |
Annual total | 9.17 | 15.80 | 18.86 | 13.88 | 15.04 | 18.81 |
Wind velocity (in miles per hour): |
Monthly mean: |
Highest | 7.0 | 6.0 | 12.3 | 7.3 | 6.5 | 10.7 |
Month | May | Apr. | Jan. | Apr. | Apr. | Apr. |
Lowest | 4.9 | 4.1 | 8.2 | 4.4 | 4.1 | 7.5 |
Month | Dec. | Dec. | Dec. | Jan. | Dec. | Oct. |
Annual mean | 6.0 | 5.0 | 10.3 | 5.9 | 5.3 | 9.1 |
There was less precipitation and a greater variation
between the 2 years of observations at M1 than at the other five
sites. The highest wind velocity measured was 30 m.p.h., in October,
when a storm was approaching.
A mantle of snow persisted only from early January to
early or mid-March. The frost-free period varied from 166 days in 1962
to 171 days in 1963. This period in each year extended from mid-May
through October.
Plant growth began at M1 earlier in the spring
than at the other mesa-top stands. Several spring perennials, Arabis
selbyii, Phlox hoodii, and Poa fendleriana, were in flower
by late March.
This type of stand is extensive at the lower
elevations on the southern part of Mesa Verde (Erdman, MS.). Evidence
from vegetational analyses and from tree-ring studies indicates that the
stand has been relatively undisturbed during the past 400 years and is
probably climax; that is, a steady-state condition in which no further
directional change in vegetation takes place under prevailing
environmental conditions (Hanson and Churchill, 1961, p. 159). However,
the present-day proportion of seedlings of the two tree species suggests
that some change may be in progress. Among the mature trees, juniper is
dominant over pine, but there are more pine than juniper seedlings. This
combination of stand characteristics may indicate that pine seedlings
are more successful than juniper in getting established but their
survival rate is lower, so that the overall proportions are constant. Or
it is possible that the present regional climate may be favoring a
subtle shift toward pine dominance (Erdman, MS.). There are differences
in the germination characteristics of the two species. Pinyon germinates
as soon as optimum moisture and temperature conditions occur (Meagher,
1943), whereas juniper requires exposure to low temperatures that occur
only in winter (Johnsen, 1959). Consequently, one might expect to find
more pine seedlings, at least in some seasons. Unfortunately, there are
no data on seedling survival.
The occurrence of bitterbrush on these heavy soils
seems to be an exception to recent findings relating to the ecology of
this species. Nord (1959, p. 2) states that in California this shrub
does not generally develop where the soil is calcareous within 3 feet of
the surface and is either imperfectly or poorly drained.
Bitterbrush, so common in this stand-type, is
undoubtedly an important factor in the abundance of deer, as it is one
of their favorite browse plants.
archeology/7b/chap3.htm
Last Updated: 16-Jan-2007
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