A study was made of factors that influence production of different numbers of flower stalks of crested wheatgrass on grazed and ungrazed areas. Both laboratory and field studies were made. Greatest response in flower stalk production resulted from application of nitrogen in the field, amounting to an increase of from 5 to 10 times the numbers of flower stalks on untreated areas. Responses of plants in the greenhouse supported these results. Plants grown in the dark indicated that higher carbohydrate reserves existed in ungrazed than in grazed plants. It was concluded that a high carbohydrate-low nitrogen balance was the primary factor in low production of flower stalks on ungrazed range. Removing photosynthetic tissue by grazing reduced the amount of root growth and amount of carbohydrates stored as reserves. On grazed range some stored carbohydrates are used in production of regrowth and new tillers giving a more favorable carbohydrate-nitrogen balance for production of flower stalks. Whether nitrogen is a primary or secondary factor in production of flower stalks depends upon the stage of plant development in which it is the limiting factor. Leachate from old growth showed no effect on production of flower stalks. Treatment with gibberellic acid suppressed flower stalk production on plants transferred to the greenhouse prior to beginning spring growth, and to a lesser extent on plants transferred after beginning spring growth. The effect was attributed primarily to the stimulation of rapid, increased growth and depletion of reserves required for differentiation and production of flower stalks. Plants produced increased numbers of flower stalks with exposure to outside cold temperatures at least up to 10 weeks' duration, which was the maximum period tested. Under field conditions, grazed plants would be subject to more rigorous temperatures than ungrazed plants, but this was believed to be a minor factor contributing to the greater numbers of flower stalks on grazed plants compared to carbohydrate-nitrogen relationships. Reduced light was shown to be a factor contributing to reduced numbers of flower stalks in the greenhouse and in an outside lath house. Reduced light was believed to be a minor factor, however, in contributing to the low numbers of flower stalks on ungrazed areas. Results of the present study indicate that the carbohydrate-nitrogen balance in plants is a better criterion for intensive management of range lands than carbohydrate reserves alone.

Fairway crested wheatgrass, which is identified taxonomically as Agropyron cristatum (L . ) Gaertn. (45 ), A. cristatiforme (38) , or A. pectiniforme Roem. and Schult (22), is an economically important range grass belonging to the "crested wheatgrass complex" (24, 38). The crested wheatgrass complex includes diploid, 2n = 14, tetraploid, 2n = 28, and hexaploid, 2n = 42, forms (1, 11, 22). The variety Fairway and Fairway-like derivatives are the only known diploid members of the species complex (24, 38). Meiotic chromosome behavior of Fairway diploids appears to be typical of other diploid species; however, the number of plants examined cytologically has been relatively small. Although Fairway crested wheatgrass is a good seed producer, interplant variation in fertility is high (13, 22, 25, 42). Irregular chromosome behavior is a common source of sterility and may be contributing to the variable seed set in diploid crested wheatgrass. No information is available concerning the relation of meiotic chromosome behavior to fertility in Fairway crested wheatgrass. Polyploid crested wheatgrasses are generally considered to be of autoploid origin, i.e., they are derived by duplication of the chromosome complement of a diploid prototype. Chromosome pairing in the polyploid species (31), in interspecific hybrids (12), and in polyhaploid plants (11) substantiate the autoploid derivation of polyploid crested wheatgrass. Diploid and tetraploid forms of crested wheatgrass have been hybridized by Knowles (24), and chromosome pairing in the hybrids suggest a close relation between the diploid and tetraploid genomes. Colchicine-induced tetraploids of Fairway crested wheatgrass have been produced by Knowles, 1 and these artificial tetraploids are currently being utilized in his crested wheatgrass breeding program. If the full breeding and cytogenetic potentials of diploid crested wheatgrass are to be realized, the meiotic chromosome behavior and the cytotaxonomic status of this species must be fully understood. The present investigation was designed to provide further information concerning the cytogenetic characteristics of Fairway crested wheatgrass and its autotetraploid derivatives. This investigation was established with the following objectives: 1. To examine meiotic chromosome behavior of Fairway crested wheatgrass. 2. To determine the relation of meiotic chromosome behavior to fertility in Fairway crested wheatgrass. 3. To evaluate the effectiveness of several colchicine treatments in doubling the chromosome complement of Fairway crested wheatgrass. 4. To determine the effect of induced polyploidy on plant morphology in colchicine-induced tetraploids of Fairway crested wheatgrass. 5. To determine the meiotic chromosome behavior and fertility of induced tetraploids of Fairway crested wheatgrass.

Crested wheatgrass (Agropyron cristatum [L.] Gaertn.) is one of the most commonly seeded grass species in the western United States and dominates thousands of hectares in the Great Basin. Although many degraded Wyoming big sagebrush (Artemisia tridentata ssp. wyomingensis) plant communities have been seeded with crested wheatgrass, successional pathways, influence of soil attributes, and cultivation history on the vegetation of these communities have not been fully characterized. I sought to identify community phases, vegetative differences, and soil attributes that explain variation among 35 Wyoming big sagebrush communities historically seeded with crested wheatgrass. All communities were more than 30 years old and had not experienced fire, or received subsequent chemical or mechanical treatments following their original seeding. Species richness, diversity, vegetation cover, and soil samples were measured in four 20 x 5 m intensive Modified Whittaker plots per community. Hierarchical clustering and principal component analysis of three indicator species (crested wheatgrass, Sandberg bluegrass, and Wyoming big sagebrush) identified four distinct community phases. Community phase 1 was dominated by crested wheatgrass and had the lowest species richness and cover of big sagebrush. Phases 2 and 3 had the highest species richness and cover of native species. Phase 4 was dominated by big sagebrush and had the lowest cover of crested wheatgrass. Community phases differed significantly for soil texture, soil nitrogen, and ground cover characteristics. Bare soil was almost double on loam-textured soils and rock cover was higher on clay loam texture soils (P < 0.05) as well as native plant cover. Communities previously cropped occurred on more coarse-textured soils and had 6-fold lower native species cover and double exotic herbaceous and crested wheatgrass cover. Cropping occurred on favorable, low rock, fine-texture soils, the same soils that favor crested wheatgrass production and reduce resilience of native plant composition. Delineation of community phases provided a new, empirically based state-and-transition model, while the characterization of soil attributes and disturbance history provided information about feedback mechanisms influencing dominant species that delineate community phases and effect community structure. This information can be used to assist in the development of management strategies in crested wheatgrass seeded communities.