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67
EFFECTS OF SHORT-DURATION GRAZING TRAMPLING ON SEEDLING EMERGENCE AND SOIL STRENGTH by JEFFREY RICHARD WEIGEL, B.A. A THESIS IN RANGE SCIENCE Submitted to the Graduate Faculty of Texas Tech University in Partial Fulfillment of the Requirements for the Degree of MASTER OF SCIENCE August, 1987

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Page 1: August, 1987 - ttu-ir.tdl.org

EFFECTS OF SHORT-DURATION GRAZING TRAMPLING ON

SEEDLING EMERGENCE AND SOIL STRENGTH

by

JEFFREY RICHARD WEIGEL, B.A.

A THESIS

IN

RANGE SCIENCE

Submitted to the Graduate Faculty of Texas Tech University in Partial Fulfillment of the Requirements for

the Degree of

MASTER OF SCIENCE

August, 1987

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1 •" ^ . i

thr t\U ff^r-^ ACKNOWLEDGEMENTS

I thank Dr. Carlton M. Britton, chairman of my graduate

cor:r.-:ittee, for his support and friendship during this study.

The members of my graduate committee, Drs. Bill E. Dahl,

B.L. Allen, and David B. Wester offered invaluable and much

appreciated assistance. Mr. Dan Griffis generously enabled

use of his ranch as a study site. John Pitts of the Texas

Tech Experimental Ranch provided welcome logistical support.

For their friendship, encouragement, and help I thank Guy

McPherson, Allen Rasmussen, Perry Grissom, Bob Masters,

Gretchen Scott, Craig Olawsky, Sheila Merrigan, Colleen

Schreiber, Sergio Soltero, Tony Leif, Meg Addison, Greg

Reeves, Jim Bergan, Doug Sheeley, and Jim Walters.

Financial support for this study was provided by the

Texas Noxious Brush and Weed Control line item. Dr. Henry

A. Wright also provided financial assistance.

I would like to thank my colleagues at The Nature

Conservancy for encouraging me to return to school and for

arranging my leave of absence.

I wish also to thank my parents, Richard and Elizabeth

Weigel, for their constant support. Finally, special thanks

and love to Mary and Moses Robert Candee for all they have

given.

11

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TABLE OF CONTENTS

ACKNOWLEDGEMENTS ii

ABSTRACT v

LIST OF TABLES vi

LIST OF FIGURES viii

CHAPTER

I. EFFECTS OF SHORT-DURATION GRAZING TRAMPLING ON SEEDLING EMERGENCE OF BROADCAST-SEEDED KLEINGRASS

(PANICUM CQLQRATUM L.) 1

Materials and Methods 3

Results and Discussion 9

Conclusions 15

II. EFFECTS OF SHORT-DURATION GRAZING ON ANNUAL FORB

AND GRASS SEEDLING EMERGENCE 17

Materials and Methods 19

Results and Discussion 23

Conclusions 27

LITERATURE CITED 28

APPENDICES

A. SOIL PROFILE DESCRIPTIONS 34

B. SOIL TEXTURE DATA 3 9

C. BASAL COVER OF PERENNIAL GRASS SPECIES 41

D. PRECIPITATION, TRAMPLING TRANSECT, AND KLEINGRASS EMERGENCE DATA, AND KLEINGRASS ANALYSIS OF VARIANCE TABLES 4 3

E. ANALYSIS OF VARIANCE TABLES FOR SOIL STRENGTH DATA 50

1 1 1

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F. FREQUENCY DATA FOR ANNUAL FORB AND GRASS SPECIES 53

IV

Page 5: August, 1987 - ttu-ir.tdl.org

ABSTRACT

Emergence of broadcast-seeded kleingrass (Panicum

COloratum L. 'Selection 75') and of native annual forbs and

grasses was compared for two seasons in short-duration

grazed areas and ungrazed exclosures. Stocking rate in

short-duration grazed areas was 2.0 and 1.5 times recommen­

ded in 1985 and 1986, respectively. Kleingrass emergence

was similar between treatments in both years. Emergence was

unrelated to percent foliar cover of preexisting vegetation.

In both study years, soil strength was greater in grazed

areas. Short-duration grazing provided no beneficial effect

on kleingrass emergence or soil strength in either year.

Emergence did not differ by treatment in either year for

five of ten species of annual forbs and two species of

annual grass. Common broomweed fXanthocephalum dracuncu-

loides (DC.) Shinners.], Texas filaree (Erodium texanum

Gray.), and meadow flax FLinum pratense (Nort.) Small.] were

more abundant in the grazed treatment in one year, while

bitterweed (Hymenoxys odorata DC.) emerged more frequently

in ungrazed areas in one season. Short-duration grazing at

the stocking rates used did not consistently improve or harm

emergence of any of the annual species studied.

Page 6: August, 1987 - ttu-ir.tdl.org

LIST OF TABLES

1.1 Rainfall prior to kleingrass emergence events in 1985 and 1986, and deviation from long-term average. 10

1.2 Hoofprint intercept means (SE) by date and mean (SE) kleingrass seedling density by date and treatment, 1985 and 1986. 11

1.3 Mean (SE) soil strength by date, grazing cycle stage, and treatment, 1985 and 1986. 13

1.4 Mean (SE) soil strength by date in hoofprints and areas without hoofprints, 1986. 14

2.1 Scientific, common, and code names of annual forbs and grasses studied, 1985-1987, 22

2.2 Percent frequency of annual forb and grass species

by season and treatment, 1985-1987. 25

B.l Soil texture data for study site soils. 40

C.l Percent basal cover of bare ground, mulch, and perennial grasses by study block, 5 August 1986. 42

D.l Kleingrass seeding and emergence dates and precipitation by day. Spring 1985 and 1986. 44

D.2 Trampling intensity in grazing cycles before

kleingrass emergence dates, 1985 and 1986. 45

D.3 Kleingrass emergence data for 25 May 1985. 46

D.4 Kleingrass emergence data for 25 April 1986. 47

D,5 Kleingrass emergence data for 6 June 198 6. 48

D.6 Analysis of variance tables for kleingrass emergence data, 1985 and 1986. 49

E.l Generalized analysis of variance table for soil strength data, 1985 and 1986. 51

E.2 Analysis of variance table for soil strength data by date, 1985 and 1986. 52

VI

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F.l Frequency data for rabbit's tobacco, common broom-weed, and woolly plantain, 1985-1987 54

F.2 Frequency data for red-seeded plantain, spurge, and bitterweed, 1985-1987. 55

F.3 Frequency data for Astragalus, Gordon's bladder-pod, and Texas filaree, 1985-1987. 56

F.4 Frequency data for meadow flax, little barley, and six-weeks fescue, 1985-1987. 57

Vll

Page 8: August, 1987 - ttu-ir.tdl.org

LIST OF FIGURES

1.1 Steers grazing near exclosures in study block six, 10 June 1985. 6

1.2 May 31, 1986 photo of study plot 81G2. 7

2.1 Deviation from average precipitation by quarterly phenological stage of annual species studied, 1985-1987. 24

Vlll

Page 9: August, 1987 - ttu-ir.tdl.org

CHAPTER I

EFFECTS OF SHORT-DURATION GRAZING TRAMPLING

ON SEEDLING EMERGENCE OF BROADCAST-SEEDED

KLEINGRASS (PANICUM CQLQRATUM L.)

Hooves of grazing animals impart physical impact on

rangeland soils and vegetation. Kind of animal, season and

intensity of grazing, soil characteristics, and plant

community influence the type and degree of impact. Range-

lands do not benefit from long-term, excessive physical

animal impact (Lull 1959, Reynolds and Packer 1963, Black­

burn et al. 1982, Blackburn 1984) .

Proponents of intensive rotational grazing systems cite

beneficial effects from increased stocking densities. The

"hoof action" of concentrated animals is said to improve

soil hydrologic properties by breaking up crusts and

increasing infiltration, thereby enhancing seedling emer­

gence (Howell 1978, Savory and Parsons 1980, Walter 1984),

Recent studies of intensive rotational grazing systems have

demonstrated detrimental impacts on soil hydrologic proper­

ties such as infiltration rate, sediment production, and

runoff (Blackburn 1984; Gamougoun et al, 1984; McCalla et

al. 1984a, 1984b; Thurow et al. 1986; Warren et al. 1986a,

1986b, 1986c, 1986d; Weltz and Wood 1986).

Page 10: August, 1987 - ttu-ir.tdl.org

2

Germination of a surface-lying seed depends on escape

from predation and placement on a site which provides appro­

priate moisture and temperature conditions (Harper et al.

1965, Sheldon 1974, Harper 1977). Modifications of soil

structure and/or microtopography by animal trampling can

influence the number of available microsites for germina­

tion. Trampling may improve the suitability for germination

of one type of microsite but reduce the suitability of

another (Stephens 1980, Eckert et al. 1986).

The ability of a seedling to emerge out of or push roots

through soil depends on relative soil strength and moisture

content as well as the emergence force exerted by the

seedling (Hanks and Thorp 1956, 1957; Taylor et al. 1966;

Taylor 1971; Jensen et al. 1972). As the soil surface

dries, soil strength increases, and emergence declines

(Stephens 1980, Hillel 1982). Trampling may increase

emergence of some species but decrease emergence of others

(Stephens 1980, Wood et al. 1982, Dahl 1986, Eckert et al.

1986, Norton and Owens 1986). Factors other than trampling

also influence seedling emergence. Wood et al. (1982) and

Dahl (1986) considered the presence or absence of competing

vegetation, and Stephens (1980) and Eckert et al, (1986)

considered soil microsite characteristics important in

determining emergence and establishment. Soil moisture

before emergence and the ability of a species to germinate

Page 11: August, 1987 - ttu-ir.tdl.org

3

under a wide variety of conditions may also exert greater

influence than trampling (Graff 1983, Dahl 1986).

This study evaluated selected impacts of short-duration

grazing on western Texas rangeland. Our hypothesis stated

that short-duration grazing trampling does not enhance

seedling emergence; this was tested using broadcast-seeded

kleingrass (Panicum coloratum L. 'Selection 75') as a

bioassay. Short-duration grazing impacts on soil compaction

were also documented.

Materials and Methods

Research was conducted in 1985 and 1986 at the Texas

Tech Experimental Ranch (101° 11' W., 32° 58' N.) 10 km

southeast of Justiceburg, Garza County, in the Texas Rolling

Plains (Gould 1969). Regional climate is semiarid, with

most of the 4 90 mm of average annual precipitation falling

from May to October (NOAA 1985) . Study plots were located

on a clay flat range site dominated by tobosagrass FHilaria

mutica (Buckl,) Benth.] and alkali sacaton rSporobolus

airoides (Torr.) Torr.] with scattered honey mesquite (Pro-

SODIS glandulosa var. glandulosa Torr.) and plains prickly-

pear (Opuntia polyacantha Haw,) (Britton and Steuter 1983) .

Soils were nearly level Stamford clays (fine, montmorillon-

itic, thermic Typic Chromusterts) with a high shrink-swell

potential, intermixed with small areas of Vernon clay loams

Page 12: August, 1987 - ttu-ir.tdl.org

4

(fine, mixed, thermic Typic Ustochrepts) (Richardson et al.

1965) ,

Before 1984, the site was moderately and continuously

grazed. It was burned in February 1983 and sprayed in July

1983 with triclopyr {[(3,5,6-trichloro-2-pyridinyl)oxy]

acetic acid}. In 1984 a six-pasture short-duration grazing

system was initiated. The 14-ha study pasture was stocked

with Hereford/Angus crossbred steers at 1.7 AUM/ha in 1985

and 1.2 AUM/ha in 1986 for three grazing cycles between

mid-April and mid-July each year. Recommended stocking for

moderate, yearlong-continuous grazing on this site is about

0,8 AUM/ha. Sixty and 42 yearling steers were used in 1985

and 1986, respectively. Stocking rate each year and grazing

and rest period lengths within years were adjusted based on

forage availability. In both years, the first two grazing

periods were seven days, followed by rest periods of 35 and

21 days in 1985 and 33 and 30 days in 1986. A final grazing

period of three days in 1985 and two days in 1986 occurred

before removal of all animals.

Immediately before grazing each season 128, 0,28-m^

plots arranged in a randomized, complete block design with

eight blocks were broadcast-seeded with kleingrass at 8,6 kg

pure live seed/ha. Kleingrass was selected because of its

adaptation to the soil and rainfall conditions of the site.

Seeding rate was intentionally heavy to insure adequate

Page 13: August, 1987 - ttu-ir.tdl.org

5

emergence to test treatment effects. Half the plots in each

block were located in randomly-placed ungrazed exclosures

(Figure 1.1) . Blocks were relocated and new plots estab­

lished for the second grazing season. Plots were located in

a 2-ha area about 550 m from the watering point of the 800-m

long triangular pasture. Grazed plots were marked below-

ground with metal stakes to avoid artificially attracting

cattle and augmenting trampling. A metal detector was used

to locate plots on sampling dates (Weigel and Britton 1986).

Kleingrass was seeded into greenhouse pots to aid field

identification. Plots were monitored twice-weekly for

kleingrass and seedlings were counted following each

emergence.

Vertical black-and-white photographs taken with a 35-rpjn

camera and 50-mm lens from 1.5 m above each plot were used

to estimate foliar cover of individual plots (Figure 1.2).

A dot-grid overlay (50 dots/grid) was used to estimate cover

on each photograph. These data were used as a covariate to

evaluate the effect of vegetative cover on kleingrass

emergence.

A proving-ring.penetrometer (Soiltest CN-970) was used

to measure soil strength (MPa) before and after each grazing

cycle each year. Soil strength is strongly correlated with

soil bulk density, a measure of soil compaction (Gifford er

al. 1977). Balph and Malachek (1985) found that livestock

Page 14: August, 1987 - ttu-ir.tdl.org

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Page 16: August, 1987 - ttu-ir.tdl.org

8

in a short-duration grazing system avoided trampling

elevated grass tussocks, so penetrometer sarr.ples were taken

only from bare soil interstices. Immediately before and

after each grazing cycle, 640 penetrometer readings

(80/block) were taken in groups of 20 closely-spaced

samples. In 1986, three of every 20 readings on dates after

grazing began were taken in visible cattle hoofprints. This

frequency of sampling corresponded to actual percent cover

of hoofprints estimated by line-intercept sampling.

Kleingrass emergence and soil strength data were

averaged over subsamples (four plots/average for kleingrass

and 20 penetr'jmeter readings/average for soil strength) ;

these data were tested for normality at each date with the

Shapiro-Wilk W-statistic (Shapiro and Wilk 1965). Block-

treatment interaction for each date was tested using Tukey's

single-degree-of-freedom test for nonadditivity at the 90%

level of significance (Steel and Torrie 1980) . Three of

four 1985 soil strength data sets demonstrated significant

interaction and were transformed using the Anscombe-Tukey

power transformation (Anscombe and Tukey 1963) . Kleingrass

emergence and soil strength data were evaluated using

analysis of variance for a randomized, complete block design

with a sampling error. Duncan's New Multiple Range Test was

used to compare soil strength data when treatments were

divided into hoofprint and non-hoofprint means. Analysis of

Page 17: August, 1987 - ttu-ir.tdl.org

9

covariance was used to assess the effect of foliar cover on

seedling emergence.

Trampling intensity was estimated by measuring hoofprint

intercepts along 16 randomly-located lO-meter line transects

immediately following the first two grazing periods each

year. Duncan's New Multiple Range Test was used to compare

hoofprint intercept means for each date. Means for the

grazing period immediately prior to each emergence event are

reported.

Results and Discussion

Adequate precipitation before and after seeding is

critical in stimulating germination (Bewley and Black 1985,

Wester et al. 1986). Precipitation during this period was

average in 1985 and above average in 1986 (Table 1.1).

Three distinct emergence events occurred during the study:

one in 1985 and two in 1986. Trampling intensity before the

single 1985 emergence was higher (P<0.05) than for the two

1986 emergences (Table 1.2) because of the higher stocking

rate in 1985.

No difference (P>0,18) in seedling emergence between

grazed and ungrazed treatments was found in either year

(Table 1.2) . Percent foliar cover of individual plots was

not a significant covariate (P>0.15) for any date,

indicating that emergence was not related to foliar cover.

In contrast, Graff (1983) obtained little or no emergence of

Page 18: August, 1987 - ttu-ir.tdl.org

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12

several broadcast-seeded grass and forb species subjected to

two levels of short-duration grazing trampling unless

competing vegetation was suppressed with herbicide prior to

seeding. In this study, no kleingrass survived to estab­

lishment in either year, probably as a consequence of

insufficient post-emergence rainfall. Virtually all seed­

lings on all emergence dates died three to seven days after

emergence.

Soil strength did not differ (P>0.40) between treatments

before grazing in 1986 (Table 1.3). There was no pre-

grazing sampling in 1985. Once grazing began, soil strength

in the grazed treatment was higher (P<0.0001) than in

ungrazed areas for all 1985 dates and four of five 1986

dates. Uniformly low soil strength in both treatments on 31

May 1986 was attributed to very wet soil conditions from

over 80 mm of rain received immediately before sampling.

On four of five 1986 post-grazing sample dates, soil

strength in hoofprints was greater (P<0.05) than in

untrampled areas within the grazed treatment (Table 1.4) ,

Soil strength in grazed, untrampled areas was not different

from ungrazed areas on three of five dates, Overall soil

strength differences between treatments (Table 1.3) were

apparently caused by the contribution of a few high-strength

hoofprints in the grazed treatment.

Page 21: August, 1987 - ttu-ir.tdl.org

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r H

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r-i

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o

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cn

/pre-2

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> i

fd 2

"^

1986

1

r-i

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r

o

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1 CD u a

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)-i

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Page 22: August, 1987 - ttu-ir.tdl.org

14

- d G fd

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> i

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2

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0) M (d

0) X> 4-» CD

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OT

CU

x: 4J > i

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p U-,

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OT C

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CM

Page 23: August, 1987 - ttu-ir.tdl.org

15

The duration of trampling impact on soil strength was

not investigated. However, evidence of recovery from

compaction between years was found. Soil strength in

second-year plots, all located in areas grazed during year

one, did not differ (P>0,40; Table 1,3) prior to second-

year grazing. This recovery was attributed to the high

shrink-swell potential of the clayey Vertisols of the site

(Larson and Allmaras 1971), Other studies of compaction

froni grazing have demonstrated recovery after rest (Warren

et al. 1986c), although more than one season may be needed

to return to the pre-compaction condition (Orr 1975,

Stephenson and Veigel 1987),

Conclusions

Suggesting that soil hydrologic condition and subsequent

seedling emergence is universally improved by livestock

trar.pling ignores the effects of soil type, soil water

consent, stocking rate, and vegetation type (Warren et al.

1986c). Trampling of sandy, crust-prone soils may reduce

compaction (Graff 1983, Tainton 1985) while finer-textured

soils may be damaged (van Haveren 1983), The impact of

trar.pling of wet soil is significantly more detrimental than

trarr.pling of dry soil (Warren et al, 1986d) ,

No beneficial effects on either emergence of broadcast-

seeded kleingrass or soil strength were realized from

seasonal short-duration grazing trampling at stocking rates

Page 24: August, 1987 - ttu-ir.tdl.org

16

2.0 and 1,5 times higher than recommended in tobosagrass-

alkali sacaton vegetation on clay soils. Conversely,

trampling did not reduce kleingrass emergence relative to

ungrazed areas. Soil compaction, as measured by soil

strength, increased in grazed areas. Presumably, soil

hydrologic properties related to soil surface condition,

such as infiltration rate, sediment production, and runoff,

would be negatively affected by increases in soil strength.

Evidence of compaction recovery between years was found.

However, the short-term nature of this study is emphasized;

documentation of longer-term impacts of seasonal short-

duration grazing is needed.

Page 25: August, 1987 - ttu-ir.tdl.org

CHAPTER II

EFFECTS OF SHORT-DURATION GRAZING ON ANNUAL

FORB AND GRASS SEEDLING EMERGENCE

Grazing, browsing, and trampling by domestic herbivores

alters vegetation and soils of rangeland communities.

Grazing-induced changes in species composition usually

reduce productivity, particularly under traditional

continuous grazing regimes (Sims et al. 1978, Heitschmidt et

al. 1982). Soil structure, microtopography, and hydrologic

properties are affected by animal physical impact (Reynolds

and Packer 1963, Blackburn et al. 1982, Eckert et al. 1986).

Animals graze selectively and patchily, and physically

impact soils and plants by trampling, pawing, and wallowing

(Spedding 1971, Polley and Collins 1984). This causes

heterogeneity in vegetation by altering competitive

relations and creating niches for colonizing species (Harper

1977). Species diversity often is higher in moderately

disturbed than in undisturbed communities (Huston 1979,

Crawley 1983, Belsky 1986). Annual species adapted for open

and disturbed environments (Grime 197 9) may contribute

significantly to increased diversity on disturbed sites

(Harper 1977).

Winter annual plants germinate in fall, overwinter in a

vegetative state, and flower, set seed, and die the

17

Page 26: August, 1987 - ttu-ir.tdl.org

18

following spring (Newman 1963). Their life cycle is closely

tied to relatively predictable fall precipitation events

which trigger mass germination (Beatley 1967, 1974). Seed­

lings develop into extremely winter-hardy basal rosettes

capable of photosynthesis at low temperatures (Bazzaz 1979) .

The winter annual strategy enables resource exploitation at

a time when dominant perennial species are largely inactive.

Range managers and researchers have directed substan­

tial effort to development of rotational grazing systems

that allow forage utilization by domestic livestock while

maintaining or improving rangeland condition. Short-

duration grazing (SDG) is an intensive, rotational grazing

system which uses relatively short grazing periods, long

rest periods, and high stocking densities to manipulate

grazing pressure, forage utilization, and subsequent forage

and livestock production (Ralphs et al. 1984). Proponents

of SDG have suggested that the system closely approximates

grazing patterns of native herbivores because dense concen­

trations of animals provide a beneficial physical animal

impact called "herd effect" (Savory and Parsons 1980, Savory

1983, Walter 1984). Herd effect purportedly improves range

condition by chipping the soil surface, thereby enhancing

infiltration, herbage production, and seedling emergence.

The objective of this study was to document emergence

and establishment of winter annual forb and annual grass

Page 27: August, 1987 - ttu-ir.tdl.org

19

species following short-duration grazing during the previous

year's flowering and seeding period. Emergence in ungrazed

exclosures was also recorded to test the hypothesis of

increased emergence with short-duration grazing trampling.

Materials and Methods

Research was conducted in a tobosagrass [Hilaria mutica

(Buckl.) Benth.]/alkali sacaton fSporobolus airoides (Torr.)

Torr.]/honey mesquite (Prosopis glandulosa var. glandulosa

Torr.) grassland in the Texas Rolling Plains (101° 11' W.,

32° 58' N.) (Gould 1969, Britton and Steuter 1983).

Regional climate is semiarid, with most of the 490 mm of

average annual precipitation falling from May to October.

Average precipitation during the fall-winter (September-

February) period of peak seedling emergence is 170 mm (NOAA

1985). Study site soils were nearly level Stamford clays

(fine, montmorillonitic, thermic Typic Chromusterts)

intermixed with small areas of Vernon clay loams (fine,

mixed, thermic Typic Ustochrepts). Stamford soils contain

predominantly montmorillonitic clays with high shrink-swell

potential (Richardson et al. 1965).

The site was moderately and continuously grazed by

domestic livestock prior to 1984. It was burned in February

1983 and sprayed with triclopyr {[(3,5,6-trichloro-2-pyri-

dinyl)oxy]acetic acid} in July 1983 for honey mesquite

Page 28: August, 1987 - ttu-ir.tdl.org

20

control. A six-pasture short-duration grazing system was

initiated in 1984. Since then, pastures have been grazed by

livestock seasonally from mid-April to mid-July each year.

Animals were sequentially rotated from pasture to pasture

during the grazing season; adjustments in length of grazing

and rest periods were based on forage growth and availabil­

ity (Savory and Parsons 1980, Savory 1983). Study plots

were located in one 14-ha pasture of the six-pasture system.

The study pasture was grazed by 60 and 42 yearling Hereford/

Angus crossbred steers for three periods in 1985 and 1986,

respectively. Stocking rates were 2.0 (1985) and 1.5 times

(1986) recommended for moderate, yearlong-continuous

grazing. In both years, the initial two grazing periods

were seven days, followed by rest periods of 35 and 21 days

in 1985 and 33 and 30 days in 1986. A final grazing period

of three days in 1985 and two days in 1986 occurred prior to

removal of all animals.

A randomized,- complete block design with eight blocks

was used. Thirty-two, O.Ol-m" plots were permanently marked

in each block, half in randomly-located ungrazed wire-mesh

exclosures (Figure 1.1). Each of four exclosures per block

contained four ungrazed plots; four groups of four grazed

plots were located nearby. Grazed plots were located at

least 3 meters from exclosures and were marked belowground

to avoid increased trampling by animals attracted to

Page 29: August, 1987 - ttu-ir.tdl.org

21

exclosure fences or aboveground plot markers. A metal

detector was used to locate plots on sampling dates (Weigel

and Britton 1986). Blocks were relocated and new plots

established prior to the second season's grazing. Plots

were located in a 2-ha area about 550 m from the single

watering point of the 800-m long triangular pasture.

Beginning with the first post-grazing emergence in

October 1985, seedling frequency of all annual species was

recorded bimonthly through February 1987, when the onset of

a third season of grazing forced termination. Sampling was

not conducted during summer when the previous season's

plants had senesced and the next season's plants had not yet

germinated. Sample dates were classified as either Season 1

(1985-1986) or Season 2 (1986-1987) based on phenology of

species studied. Four and three sample dates comprised

Seasons 1 and 2, respectively.

Species recorded in at least 5% of plots for any

date-treatment combination were analyzed for treatment

response (Gauch 1982). Data were summarized in a 2 X 4

(Season 1) or 2 X 3 (Season 2) contingency table and

analyzed with a log-linear model that included treatment,

date, and a response variable (frequency) (Bishop et al.

1975) .

Page 30: August, 1987 - ttu-ir.tdl.org

22

Results and Discn.s.sion

Ten species of winter annual forbs and two species of

annual grass were analyzed (Table 2.1). Six additional

species of annual forbs were encountered but not analyzed

because of low frequencies for each date-treatment combina­

tion ,

Above normal fall precipitation in both seasons created

apparently excellent germination conditions both years

(Figure 2.1). However, frequencies of five of the six most

common forbs (rabbit's tobacco, common broomweed, woolly

plantain, red-seeded plantain, and bitterweed) and the most

common annual grass (little barley) were substantially

higher in Season 1 regardless of treatment (Table 2.2).

Lower frequency of these species in Season 2 may have been

related to very low Season 1 winter precipitation and very

high Season 2 fall precipitation. Many Season 1 seedlings

died before flowering or seeding, so fewer seeds were

available for germination the following fall. Beatley

(1974) attributed late-winter mortality of Mojave Desert

annuals to decreased soil moisture during this critical

growth period, although some mortality occurred even in

years with adequate moisture. Several researchers have

demonstrated density-dependent thinning in desert annuals

(see Fowler 1986 for a review). Season 2 fall precipita­

tion occurred early in that period, and was nearly twice

Page 31: August, 1987 - ttu-ir.tdl.org

23

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Page 32: August, 1987 - ttu-ir.tdl.org

24 so

n 1

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ese

s

on

b

stu

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tica

are

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es

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in

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(mm

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ure

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ts

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om

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ure

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19

85

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87

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(%) aOejaAB luoj^ uojiejAap

Page 33: August, 1987 - ttu-ir.tdl.org

25

Table 2.2, Percent frequency of annual forb and grass species by season and treatment, 1985-1987,

Species-^

Forbs:

E W E

XADR

PLPA

PLRH

EUSP

HYOD

ASSP

LEGO^

ERTE

LIPR

Grasses:

HOPU

VUOC

Season

ungrazed

93.5

49.6^

52.7

36.1

25.0

11.7'

4.3

3.9

2.3

3.1

31.2-

1.4

.4

*:•

ll

grazed

91.6

55.7

49.0

36.5

28.3

6.8

4.9

3.1

3.3

1.8

34.6

2.3

Season

ungrazed

69.3

35.2

25.8

27.9

33.9

3.6

7 .8

6.5

2,1***

0,1***

11.7

2.3

22

grazed

70.3

38.8

25,3

24.2

28.4

3.4

6.5

5,5

7.3

4.7

12.5

1.6

^n = 4 sample dates (10/27/85, 11/29/85, 2/4/86, 4/5/86)

^n = 3 sample dates (10/14/86, 12/16/86, 2/4/87) .

^Species codes listed in Table 2.1,

^Different than frequency in grazed areas at P<0.05 (*), P<0.01 (**), and P<0.001 (***).

^Significant (P<0.05) 3-way interaction in Season 1,

Page 34: August, 1987 - ttu-ir.tdl.org

26

average (Figure 2.1), This stimulated vigorous growth of

perennial grass dominants, which may have reduced germina­

tion and survival of annuals by preemptive use of soil

moisture (Friedman et al. 1977).

Five of ten winter annual forb and both annual grass

species showed no difference between treatments in both

seasons (Table 2.2) . In Season 1, frequency of common

broomweed was greater in grazed plots, while frequency of

bitterweed was higher in ungrazed exclosures. A 3-way

interaction (P<0.05) for Gordon's bladderpod indicated that

frequency varied by date and treatment.

Gordon (1982) found significant negative correlations

between broomweed emergence and biomass of standing dead

herbaceous material and litter, indicating that lower

broomweed emergence could be expected in ungrazed areas.

Season 1 results in this study support this conclusion.

The response of bitterweed was not expected. Bitterweed is

a poisonous, unpalatable species, considered an "increaser"

by range managers, yet it occurred more frequently in

ungrazed plots. No differences by treatment for broomweed

or bitterweed emergence were found in Season 2.

Texas filaree and meadow flax emerged more frequently

in grazed plots than in ungrazed plots in Season 2. Filaree

apparently preferred bare areas, which were less common in

ungrazed exclosures. Baker (1974) considered the genus

Page 35: August, 1987 - ttu-ir.tdl.org

27

Erpcjiiym, with its prostrate vegetative rosette and seed

morphology conducive to animal dispersal, to be well-adapted

to animal trampling. Greater presence of meadow flax in

grazed plots was not readily explainable.

Conclusions

Precipitation at critical life history stages is the

primary factor controlling germination and survival of

winter annual forbs and annual grasses. Large fluctuations

in annual populations between years are common (Beatley

1967, 1974) . Livestock trampling at the stocking rates used

in this study provided no consistent beneficial or harmful

impact to any of the annual species studied. The short-term

nature of the study is emphasized; impacts on annual species

over longer periods of short-duration grazing are needed.

Page 36: August, 1987 - ttu-ir.tdl.org

LITERATURE CITED

Anscombe, F.J., and J.W. Tukey. 1963. The examination and analysis of residuals. Technometrics 5:141-160.

Baker, H.G. 1974. The evolution of weeds. Ann. Rev. Ecol. Syst. 5:1-24.

Balph, D.F., and J.C. Malachek. 1985. Cattle trampling of crested wheatgrass under short-duration grazing trampling. J. Range Manage. 38:226-227.

Bazzaz, F.A. 1979. The physiological ecology of plant succession. Ann. Rev. Ecol, Syst. 10:351-371.

Beatley, J.C. 1967. Survival of winter annuals in the northern Mojave Desert. Ecology 48:745-750.

Beatley, J.C. 1974. Phenological events and their environmental triggers in Mojave Desert ecosystems. Ecol. 55:856-863.

Belsky, A.J. 1986. Revegetation of artificial disturbances in grasslands of the Serengeti National Park, Tanzania. I. Colonization of grazed and ungrazed plots. J. Ecol. 74:419-437,

Bewley, J,D., and M. Black. 1985. Seeds: physiology of development and germination. Plenum Press, New York,

Bishop, Y.M., S.E. Fienberg, and P.W. Holland. 1975. Discrete multivariate analysis: theory and practice, MIT Press, Cambridge, Mass.

Blackburn, W.H. 1984. Impacts of grazing intensity and specialized grazing systems on watershed characteristics and responses, p. 927-983. In: Developing strategies for rangeland managemient. National Research Council/National Academy of Sciences, Westview Press, Boulder, CO.

Blackburn, W.H., R.W. Knight, andM.K. Wood. 1982. Impacts of grazing on watersheds: a state of knowledge, Texas Agr. Exp. Sta. Rep. MP-14 96.

Britton, CM., and A.A. Steuter. 1983. Production and nutritional attributes of tobosagrass following burning. Southwest. Natur. 28:347-352.

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Correll, D.S., and M.C. Johnston. 1970. Manual of the vascular plants of Texas. Texas Res. Found., Renner, TX.

Crawley, M.J. 1983. Herbivory - the dynamics of animal-plant interactions. Univ, Cal, Press, Los Angeles.

Dahl, B.E. 1986. The west Texas experience in short duration grazing, p. 103-116. In: J.A. Tiedeman (ed.). Short duration grazing: Proc. short duration grazing and current issues in grazing manage, shortcourse. Wash. State Univ., Pullman.

Eckert, R.E., Jr., F.F. Peterson, M.S. Meurisse, and J.L. Stephens. 1986. Effects of soil-surface morphology on emergence and survival of seedlings in big sagebrush communities. J, Range Manage. 39:414-420,

Fowler, N.L. 1986. The role of competition in plant communities in arid and semiarid regions. Ann. Rev. Ecol. Syst. 17:89-110.

Friedman, J., G. Orshan, and Y, Ziger-Cfir. 1977, Suppre-sion of annuals by Artemesia herba-alba in the Negev Desert of Israel, J. Ecol. 65:413-426.

Gamougoun, N.D., R.P. Smith, M.K. Wood, and R.D. Pieper. 1984, Soil, vegetation, and hydrologic responses to grazing management at Ft, Stanton, New Mexico. J. Range Manage. 37:538-541.

Gauch, H.G. 1982. Multivariate analysis in community ecology. Cambridge Univ. Press, New York.

Gifford, G.F., R.H-. Faust, and G.B. Coltharp. 1977. Measuring soil compaction on rangeland. J. Range Manage. 30:457-460.

Gordon, R.A. 1982. The ecology and control of common broomweed. Ph.D. Diss. Texas Tech Univ., Lubbock.

Gould, F.W. 1969. Texas plants: a checklist and ecological summary. Texas Agr. Exp. Sta. Rep. MP-585.

Graff, P.S. 1983. Trampling effect on seedling production and soil strength under short-duration and continuous grazing. M.S. Thesis. Texas Tech Univ., Lubbock.

Grime, J.P. 1979. Plant strategies and vegetation processes. J. Wiley Pub., Inc., New York.

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Hanks, R.J., and F.C. Thorp. 1956. Seedling emergence of wheat as related to soil moisture content, bulk density, oxygen diffusion rate, and crust strength. Soil Sci. Soc. Amer. Proc. 20:307-310.

Hanks, R,J., and F.C. Thorp. 1957. Seedling emergence of wheat, grain sorghum, and soybeans as influenced by soil crust strength and moisture content. Soil Sci. Soc. Amer. Proc. 21:357-359.

Harper, J.L. 1977. Population biology of plants. Academic Press, London.

Harper, J.L., J.T. Williams, and G.R. Sagar, 1965. The behavior of seeds in soil. I. The heterogeneity of soil surfaces and its role in determining the establishment of plants from seed. J. Ecol. 53:273-286,

Heitschmidt, R.K., J,R. Erasure, D.L. Price, and L.R. Rittenhouse. 1982. Short duration grazing at the Texas Experimental Ranch: weight gains of growing heifers. J. Range Manage. 35:375-379.

Hillel, D. 1982. Introduction to soil physics. Academic Press, New York.

Howell, L.N. 1978. Development of multi-camp grazing systems in the Southern Orange Free State, Republic of South Africa. J. Range Manage. 31:459-465,

Huston, M. 1979. A general hypothesis of diversity. Amer, Nat. 113:81-101.

Jensen, E.H., J.R. Frelich, and R.O. Gifford. 1972. Emergence force of forage seedlings. Agron. J. 64:635-639.

Larson, W.E., and R.R. Allmaras. 1971. Management factors and natural forces related to compaction, p. 367-427. In: K.K. Barnes et al. (eds.). Compaction of agricul­tural soils. Amer. Soc. Agr. Eng. Monogr. No. 1.

Lull, H.W. 1959. Soil compaction in forest and range lands. USDA Misc. Pub. 768.

McCalla, G.R., W.H. Blackburn, and L.B. Merrill. 1984a. Effects of livestock grazing on infiltration rates, Edwards Plateau of Texas. J. Range Manage. 37:265-269

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31

McCalla, G.R., W.H. Blackburn, and L.B. Merrill. 1984b. Effects of livestock grazing on sediment production, Edwards Plateau of Texas. J. Range Manage. 37:291-194

National Oceanic and Atmospheric Administration. 1985. Climatological data annual summary - Texas 1984. Vol. 89, No. 13.

Newman, E.I. 1963. Factors controlling the germination date of winter annuals. J. Ecol. 51:625-638.

Norton, B.E., and Owens, M.K. 1986. Studies in short duration grazing on crested wheatgrass pastures in Utah, p. 83-90. In: J.A. Tiedeman (ed.). Short duration grazing: Proc. short duration grazing and current issues in grazing manage, shortcourse. Wash. State Univ., Pullman.

Orr, H.K. 1975. Recovery from soil compaction on bluegrass range in the Black Hills. Trans. Amer. Soc. Agr. Eng. 18:1076-1081.

Polley, H.W., and S.L. Collins. 1984. Relationships of vegetation and environment in buffalo wallows. Amer. Midi. Nat. 112:178-186.

Ralphs, M.H., M.M. Kothmann, and L.B. Merrill. 1984. Proper stocking for short duration grazing. Texas Agr, Exp. Sta. Rep. PR-4190.

Reynolds, H.G., and P.E. Packer. 1963. Effects of trampling on soil and vegetation. USDA Misc. Pub. 940

Richardson, W.E., D.G. Grice, and L.A. Putnam. 1965. Soil survey of Garza County, Texas. USDA Soil Cons. Serv.

Savory, A. 1983. The Savory Grazing Method or Holistic Resource Management. Rangelands 5:155-159.

Savory, A., and S. Parsons. 1980. The Savory Grazing Method. Rangelands 2:234-237.

Shapiro, S.S., and M.B. Wilk. 1965. An analysis of variance test for normality (complete samples). Biometrika 52:591-611.

Sheldon, J.C. 1974. The behaviour of seeds in soil. III. The influence of seed morphology and the behaviour of seedlings on the establishment of plants from surface-lying seeds. J. Ecol. 62:47-66.

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32

Sims, P.L., J.S. Singh, andW.K. Lauenroth. 1978. The structure and function of ten western North American grasslands. I, Abiotic and vegetational characteris­tics, J, Ecol, 66:251-285,

Spedding, C.R.W. 1971, Grassland ecology, Oxford Univ, Press, London.

Steel, R,G,D., and J,H. Torrie. 1980, Principles and procedures of statistics. McGraw-Hill Book Co., Inc., New York.

Stephens, J.L, 1980. Seedling emergence on vesicular crusted surfaces as affected by artifical and natural cattle trampling. M.S. Thesis. Univ. Nevada-Reno.

Stephenson, G.R., and A. Veigel. 1987. Recovery of compacted soil on pastures used for winter cattle feeding. J. Range Manage. 40:4 6-48.

Tainton, N.M, 1985. Recent trends in grazing management philosophy in South Africa. J. Grassl. Soc. S. Afr. 2:4-6.

Taylor, H.M. 1971. Effects of soil strength on seedling emergence, root growth, and crop yield, p. XX-ZZ. In: K.K Barnes, et al. (eds,). Compaction of agricultural soils. Amer. Soc. Agr. Eng. Monogr. No, 1.

Taylor, H.M., J.J. Parker, and G.M. Roberson. 1966. Soil strength and seedling emergence relations. II. A generalized relation for Gramineae. Agron. J. 58:393-395.

Thurow, T.L., W.H. Blackburn, and C A . Taylor. 1986. Hydrologic characteristics of vegetation types as affected by livestock grazing systems, Edwards Plateau, Texas. J. Range Manage. 39:505-50 9.

van Haveren, B.P. 1983. Soil bulk density as influenced by grazing intensity and soil type on a shortgrass prairie site. J. Range Manage. 36:586-588.

Walter, J. 1984 . Rangeland revolutionary: an interview with Allen Savory. J. Soil and Water Cons, 39:235-240.

Warren, S.D., W.H. Blackburn, and C A . Taylor, Jr. 1986a. Effects of season and stage of rotation cycle on hydrologic condition of rangeland under intensive rotation grazing. J. Range Manage. 39:486-491.

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Warren, S.D., W.H. Blackburn, a n d C A . Taylor, Jr. 1986b. Soil hydrologic response to number of pastures and stocking density under intensive rotation grazing. J. Range Manage. 39:500-504.

Warren, S.D,, M,B. Nevill, W.H. Blackburn, andN.E. Garza. 1986c. Soil response to trampling under intensive rotation grazing. Soil Sci. Soc. Amer. J. 50:1336-1341.

Warren, S.D., T.L. Thurow, W.H. Blackburn, and N.E. Garza. 1986d. The influence of livestock trampling under intensive rotation grazing on soil hydrologic characteristics. J. Range Manage. 39:491-495.

Weigel, J.R., and C M . Britton. 1986. Use of a metal detector to locate permanent plots. J. Range Manage, 39:565,

Weltz, M., and M.K. Wood. 1986. Short duration grazing in central New Mexico: effects on infiltration rates, J. Range Manage, 39:365-368.

Wester, D,B,, B,E. Dahl, and P.F. Cotter, 1986. Effects of pattern and amount of simulated rainfall on seedling dynamics of weeping lovegrass and kleingrass. Agron. J, 78:851-855,

Wood, M,K., R,E. Eckert, Jr., W.H. Blackburn, and F.F. Peterson. 1982. Influence of crusting soil surfaces on emergence and establishment of crested wheatgrass, squirreltail, Thurber needlegrass, and fourwing saltbush. J, Range Manage. 35:282-287,

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APPENDIX A

SOIL PROFILE DESCRIPTIONS

34

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35

Soil Series: Stamford

General Description: Soils formed from clayey, micaceous

Triassic redbed material on gently sloping alluvial flats.

This series consists of deep, very slowly permeable but

v;ell-drained soils with high shrink-swell potential. Gilgai

microrelief and dry-season cracks up to 50 cm deep are

present,

Pedon Al: Typical pedon from short duration grazing cell 1,

pasture 2 .

Al—0 to 15 cm; dark reddish brown (2.5YR 3/4) clay; dark

reddish brown (2.5YR 2.5/4) moist; weak platy in upper 2 cm,

otherwise weak subangular blocky structure; firm; strong

effervescence; common medium roots; gradual, smooth

boundary.

A2--15 to 50 cm; dark reddish brown (2.5YR 3/4) clay; dark

reddish brown (2.5YR 2.5/4) moist; moderate subangular

blocky structure; very firm; strong effervescence; common

medium roots; gradual smooth boundary.

Bw—50 to 78 cm; reddish brown (2.5YR 4/4) clay; dark

reddish brown (2.5YR 3/4) moist; moderate subangular and

angular blocky structure; very firm; common medium

slickensides, some intersecting; discontinuous areas of

common calcium carbonate concretions; strong effervescence;

common fine roots; clear, wavy boundary.

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36

Bk—78 to 98 cm; reddish brown (2,5YR 4/4) clay; aark

reddish brown (2.5YR 3/4) moist; weak subangular blocky

structure; very hard; violent effervescence; few fine roots;

clear, wavy boundary,

BC—98 to 116 cm; reddish brown (2,5YR 4/4) clay; dark

reddish brown (2.5YR 3/4) moist; weak subangular blocky

structure; very hard; violent effervescence; very few fine

roots; gradual, smooth boundary.

Cr—116+ cm; red (2.5YR 4/6) loam; reddish brown (2.5YR 4/4)

moist; massive; hard; strong effervescence.

Pedon All: Shallower pedon near well-defined drainage in

short duration grazing cell 1, pasture 2.

A — 0 to 13 cm; dark reddish brown (2.5YR 3/4) clay; dark

reddish brown (2.5YR 2.5/4) moist; weak platy in upper 2 cm,

otherwise granular and weak subangular blocky structure;

friable; strong effervescence; many fine and medium roots;

clear, smooth boundary.

Bwl—13 to 34 cm; reddish brown (2,5YR 4/4) clay; dark

reddish brown (2.5YR 2.5/4) moist; weak prismatic breaking

to moderate subangular blocky structure; firm; strong

effervescence; common fine and medium roots; gradual, smiooth

boundary.

Bw2--34 to 61 cm; reddish brown (2.5YR 5/4) clay; dark

reddish brown (2.5YR 3/4) moist; weak prismatic breaking to

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37

angular and subangular blocky structure; firm; weak

slickenside development; strong effervescence; few fine

roots; gradual, wavy boundary.

Bk—61 to 83+ cm; red (2.5YR 4/6) clay loam; reddish brown

(2.SYR 4/4) moist; weak subangular blocky structure; very

hard; violent effervescence; very few fine roots.

Series: Vernon

General Description: Soils formed from clayey Triassic

redbed material on footslopes, convex ridges, and along

shallow drainageways. This series consists of moderately

deep, very slowly permeable but well-drained soils underlain

by partially weathered redbed shale.

Pedon BI: Typical pedon from short duration grazing cell 1,

pasture 2.

A — 0 to 9 cm; reddish brown (2.5YR 4/4) clay loam; dark

reddish brown (2.5YR 3/4) moist; weak subangular blocky

structure; friable; violent effervescence; common fine and

medium roots; clear, smooth boundary.

Bw—9 to 27 cm; reddish brown (2.5YR 5/4) clay; reddish

brown (2.5YR 4/4) moist; moderate subangular blocky and weak

prismatic structure; very firm; violent effervescence;

common fine roots; clear, irregular boundary.

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38

Bk--27 to 48 cm; red (2.5YR 5/6) clay; red (2.5YR 4/6)

moist; discontinuous areas of common pink (5YR 7/4) calcium

carbonate concretions, light reddish brown (5YR 6/4) moist;

inherited shale parting; very hard; violent effervescence;

few fine roots; clear, wavy boundary.

Cr—48 to 68+; light red (2.5YR 6/6) shale; red (2.5 YR 5/6)

moist; massive; light effervescence; very few fine roots.

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APPENDIX B

SOIL TEXTURE DATA

39

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40

Table B.l, Soil texture data for study site soils.

Pedon

Al -

All -

BI -

Stamford

Stamford

Vernon

Horizon

Al

A2

Bw

Bk

BC

Cr

A

Bwl

Bw2

Bk

Bk

A

Bw

Bk

Cr

(lower)

Sand

15.7

13.0

13.1

20.5

16.6

60.0

29.7

22.9

15.4

33,2

23,3

33.6

11.4

13.7

25.1

Percent Silt

35.6

34.5

38.9

44 .0

37.2

24 .1

38.3

37.1

39.4

34 .0

53.5

45.5

42.9

55.0

50.2

Clay

48.7

52.6

48.1

35.6

46.2

24.9

32.0

40.0

45.2

32.8

23.2

20.9

45.7

31.4

24.6

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APPENDIX C

BASAL COVER OF PERENNIAL GRASS SPECIES

41

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42

Table C.l. Percent basal cover of bare ground, mulch, and perennial grass by study block, 5 August 1986.

Block^ Class or species

BARE MULCH HIMU SPAI SCPA BUDA SPPY

1

2

3

4

5

6

7

8

63.2

60.0

72.8

49.2

69.8

43.8

36.6

50.4

28,8

31,2

20.2

40.0

20.8

43.4

53.0

39.4

5,4

3.4

2.2

1.4

1.4

8.8

8.8

4.2

2 . 6

5 . 2

1 , 4

9 . 4

0 . 0

0 , 2

0 , 0

0 . 0

6,6

4,0

1.0

5.6

0.4

0.0

0,0

0.0

0.0

0.0

3,2

0.0

0,0

0.0

0.6

0.4

0.0

0.0

0.2

0.0

1.0

0.0

0.0

0.0

X 55.7 34 .6 4.4 4.5 0.1 0.5 0.2

In = conducted in grazed areas

500 ten-point-frame sample points per block; sampling

^BARE = bare ground, MULCH = mulch, HIMU = Hilaria mutica^

SPAI = .sporoboius a i r o i d e s , SCPA = Schedonnacdus panicu-latus, BUDA = Bnchloe dactyloides. SPPY = SporoboluS 2.y£-amidatus.

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APPENDIX D

PRECIPITATION, TRAMPLING TRANSECT, AND KLEINGRASS

EMERGENCE DATA, AND KLEINGRASS ANALYSIS OF

VARIANCE TABLES

43

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44

Table D.l. Kleingrass seeding and emergence dates and precipitation by day. Spring 1985 and 1986.

Sorina 1qfiS

Date

21 April

28 April

28 April

0 6 May

08 May

13 May

16 May

17 May

21 May

22 May

25 May

05 June

0 6 June

11 June

ppt (mm)

9.1

seeding

30.5

10.4

11.2

5,1

17,5

2.0

10.2

8.9

emergence

42,2

16,3

15,0

Sprina 1986

Date

27

02

06

19

24

25

25

26

27

30

01

03

05

06

17

19

March

April

April

April

April

April

May

May

May

May

June

June

June

June

June

June

ppt (mm)

seeding

16.5

7.6

56.6

4.1

emergence

9,6

10,7

27.4

35.6

33.5

11.9

4,8

emergence

23.9

38.9

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45

Table D,2, Trampling intensity in grazing cycles before kleingrass emergence dates, 1985 and 1986.

Sample Date: 14 May 1985 23 April 1986 31 May 1986

Emergence Date: 25 May 1985 25 April 1986 06 June 1986

% Hoofprints / 10.0 m

42.5

24.1

16.4

16.9

12.0

3.1

11.3

10.3

27,4

17,6

7.1

18.2

29.3

9.4

31.6

14.0

X = 18.2 X =

S.E. = 2.6 S.E, = 1,8 S.E. = 1.6

2 6 , 6

9 , 8

6 , 9

1 1 , 6

1 1 . 3

4 . 3

2 3 . 4

1 3 . 5

7 . 0

1 9 . 7

3 . 0

8 . 2

1 0 . 2

3 . 4

5 . 2

1 6 . 7

1 1 . 3

6 . 0

1 6 . 0

1 3 . 0

1 0 . 0

2 2 . 0

2 8 . 5

4 . 0

1 3 . 5

1 6 . 0

7 . 5

9 . 5

14 .0

1 5 . 5

1 0 . 5

17 . 0

2 3 . 0

X = 14 . 1

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46

T a b l e D . 3 . K l e i n g r a s s emergence d a t a fo r 25 May 1985.

Block.

1 1 1 1

2 2 2 2

3 3 3 3

4 4 4 4

5 5 5 5

6 6 6 6

7 7 7 7

8 8 8 8

Quadrant

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

Treatment

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

No

1

6 5 14 7

4 4 7 10

11 9 5 9

2 7 1 7

3 7 2 9

10 6

11 28

3 1 0 7

3 4 3 1

. see plot

2

11 9 8 4

6 1 7

20

13 8 7 6

5 4

11 5

19 5

12 9

9 6 8

13

3 3 3 5

3 0 0 3

dlings number

3

12 4 6

10

5 3 8 9

4 13 18 2

6 6 4

13

6 13 9 9

6 14 9

25

0 0 4 3

1 5 1 1

in

4

3 24 8 7

11 2 6 1

17 8

11 8

5 10 2

20

5 2 5 10

26 11 7 14

0 9 2 4

0 2 6 4

Ave^

8.0 10.5 9.0 7.0

6.5 2.5 7,0 10.0

11.2 9.5

10.2 6.2

4.5 6.7 4.5

11.2

8.2 6.7 7.0 9.2

12.7 9,2 8.7

20.0

1.5 3.2 2.2 4.7

1.7 2.7 2.5 2.2

0 = ungrazed, 1 = grazed.

Average of four p l o t s in row,

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47

Table D.4 . K le ing ra s s emergence data for 25 Apr i l 1986

Block

1 1 1 1

2 2 2 2

3 3 3 3

4 4 4 4

5 5 5 5

6 6 6 6

7 7 7 7

8 8 8 8

Quadrant

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

Treatment

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

No. p

1

1 1

14 6

11 0 3 5

0 0 0 0

2 1 7 6

7 14 22 14

4 0 6 3

13 1

15 24

1 6 9 8

seedlings lot

2

1 8

31 6

17 2 5 3

2 0 0 0

7 5 4 0

28 17 11 7

6 24 10 6

41 17 30 29

8 17 18 40

number

3

4 0

44 8

12 0 9

14

0 1 0 0

9 2 3 4

22 12 18 6

13 8 5

18

30 5

24 35

12 8

18 21

in

4

7 3

24 13

8 2 0

20

0 17 0 0

1 JL

5 1

12 23 24 13

14 4 5 5

7 0

15 14

3 1 3 11

Ave^

3.2 3.0

28.2 8.2

12.0 1.0 4.2

10.5

0.5 4.5 0.0 0.0

4.7 2.5 4.7 2.7

17.2 16.5 18.7 10.0

9.2 9.0 6.5 8.0

22.7 5.7

21.0 25.5

6.0 8.0

12.0 20.0

• 0 = ungrazed, 1 = grazed.

Average of four p l o t s in row.

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48

Table

Block

1

1 1 1

2 2 2 2

3 3 3 3

4 4 4 4

5 5 5 5

6 6 6 6

7 7 7 7

8 8 8 8

D.5. Kleingrass

Quadrant

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

1 1 2 2

emergence

Treatment

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

0 1 0 1

data

No

1

3 15 8 3

6 0

13 13

2 6 3 6

25 9

17 10

9 2 5

17

20 14 5 4

15 16 11 9

13 15 4

17

for 1

. see plot

2

15 4

16 2

15 10 3 5

17 5 4 5

21 11 16 10

16 19 5 5

10 27 14 3

18 15 17 16

16 13 12 16

5 June

dlings number

3

11 3

11 3

15 5 11 11

2 6

12 12

14 8

26 13

18 7 13 5

20 18 13 10

15 18 17 12

26 8

11 7

1986.

in

4

11 5 1 2

19 3

20 8

7 20 4 7

30 13 17 15

14 7

16 29

16 6 7 3

7 21 7

29

9 17 7 3

2 Ave^

10.0 6.7 9.0 2.5

13.7 4.5

11.7 9.2

7.0 9.2 5.7 7.5

22.5 10.2 19.0 12.0

14.2 8.7 9.7

14.0

16.5 16.2 9.7 5.0

13.7 17.5 13.0 16.5

16.0 13.2 8.5 10.7

0 = ungrazed, 1 = grazed.

Average of four plots in row,

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/ 9

Table D.6. Analysis of variance tables for kleingrass emergence data, 1985 and 1986.

Date; 25 May iqRS

Source Degrees Sum of of Variation of Freedom Squares F Prob > F

Blocks 7

Treatments 1 8.2519 1.43 0.2707

Blk X Trt (Exp. Error) 7 40.3887

Sampling Error 16

Total 31

Date; 25 April 1986

Source Degrees Sum of of Variation of Freedom Squares E Pirob > F

Blocks 7

Treatments

Blk X Trt (Exp.

Sampling Error

Total

1

Error) 7

16

31

40.5000

163.1875

1,74 0,2290

Date: 06 June 1986

Source Degrees Sum of of Variation of Freedom Squares E Frob > F

Blocks 7

Treatments 1 41.0645 2.15 0.1860

Blk X Trt (Exp, Error) 7 133.7012

Sampling Error 16

Total II

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APPENDIX E

ANALYSIS OF VARIANCE TABLES FOR SOIL

STRENGTH DATA

50

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51

Table E.l, Generalized analysis of variance table for soil strength data, 1985 and 1986.

Source Degrees

of Variance of Freedom

Blocks 7

Treatments 1

Blk X Trt (Exp. Error) 7

Sampling Error 48

Total 63

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52

Table E,2. Analysis of variance table for soil strength data by date, 1933 and 1986.

Sum of Squares

Date Treatment B X T F Prob > F

5-06-85 0.2650 0,1330 13.95 0.0073

6-09-85^ 0.003800 0.000164 162.20 0.0001

6-18-85^ 0.176129 0,005550 222.14 0.0001

7-08-85^ 2,2762 0.1991 80.01 0,0001

3-20-86 0.001279 0.011479 0.78 0.4064

4-13-86 0.000067 0.063866 0.01 0.9341

4-23-86 0.2723 0.0232 82.33 0.0001

5-14-86 0.4264 0.0410 72.82 0.0001

5-25-86 0.3338 0.0152 153.37 0.0001

5-31-86 0.0013 0.0047 1.96 0.2041

7-16-86 1.2905 0.0814 110.96 0.0001

Analysis on power-transformed data.

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wqwpip

APPENDIX F

FREQUENCY DATA FOR ANNUAL FORB AND

GRASS SPECIES

53

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54

Table F.l. Frequency data for rabbit's tobacco, common broomweed, and woolly plantain, 1985-1987.

Frequency (No. plots with plants)

Season 1 Season 2

Species Date Ungrazed Grazed Ungrazed Grazed

E W E

XADR

PLPA

1

CN

00

4

Total plots

% frequency

1

2

3

4

Total plots

% frequency

1

2

3

4

Total plots

% frequency

12 8

12 5

12 3

103

4 7 9

93.5

62

73

71

48

2 5 4

49.6

63

68

72

67

2 7 0

52.7

12 7

12 7

115

100

4 6 9

91.6

74

91

67

53

2 8 5

55.7

66

68

62

55

2 5 1

49.0

86

96

84

2 6 6

69.3

44

45

46

13 5

35.2

31

35

33

99

25.8

93

91

86

2 70

70.3

52

52

45

14 9

38.8

24

35

38

97

25.3

n = 128 total possible plots/date-treatment combination.

Page 63: August, 1987 - ttu-ir.tdl.org

55

^^^•^^•5'^' ^^equency data for red-seeded plantain, spurge, and bitterweed, 1985-1987.

Species Date

r-i

2 PLRH

3

4

Total plots

% frequency

1

2 EUSP

3

4

Total plots

% frequency

1

2 HYOD

3

4

Total plots

% frequency

Frequ

Seas

Ungrazed

84

42

34

25

18 5

36.1

53

44

24

7

12 8

25.0

21

15

16

8

60

11.7

ency (No.

on 1

Grazed

95

33

30

29

187

36.5

61

50

23

11

14 5

28.3

11

8

6

10

35

6.8

plots with plants)

Season 2

Ungrazed

41

36

30

10 7

27,9

28

53

49

13 0

33,9

4

4

6

14

3.6

Grazed

32

34

27

93

24 .2

23

43

43

10 9

28.4

4

6

3

13

3.4

n = 128 total possible plots/date-treatment combination

Page 64: August, 1987 - ttu-ir.tdl.org

56

Table F.3. Frequency data for Astragalus, Gordon's bladderpod, and Texas filaree, 1985-1987.

Species Date

1

2 ASSP

3

4

Total plots

% frequency

1

2 LEGO

3

4

Total plots

% frequency

1

2 ERTE

3

4

Total plots

% frequency

Ung

Frequ ency (No.

Season 1

razed

5

4

4

9

22

4.3

7

5

3

5

20

3.9

4

5

2

1

12

2.3

Grazed

7

7

5

6

25

4.9

5

3

8

0

16

3.1

5

3

4

5

1 7

3.3

plot

Ung

s with plants)

Season 2

razed

15

9

6

30

7.8

9

7

9

25

6.5

4

2

2

8

2.1

Grazed

12

6

7

25

6.5

9

6

6

21

5.5

13

7

8

28

7.3

n = 128 total possible plots/date-treatment combination

Page 65: August, 1987 - ttu-ir.tdl.org

57

Table F.4. Frequency data for meadow flax, little barley, and six-weeks fescue, 1985-1987.

Frequency (No. plots with plants)

Season 1 Season 2

Species Date Ungrazed Grazed Ungrazed Grazed

LIPR

HOPU

PLPA

1

2

3

4

Total plots

% frequency

1

2

3

4

Total plots

% frequency

1

2

3

4

Total plots

% frequency

4

4

3

5

16

3.1

49

57

52

2

160

31.2

63

68

72

67

2 70

52.7

3

1

2

3

9

1.8

55

61

60

1

17 7

34.6

66

68

62

55

2 5 1

49.0

0

1

0

1

0,1

3

19

23

45

11,7

31

35

33

99

25.8

2

9

7

18

4,7

6

23

19

48

12,5

24

35

38

97

25.3

n = 128 total possible plots/date-treatment combination.

Page 66: August, 1987 - ttu-ir.tdl.org

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