Biology:Pseudoroegneria spicata
| Bluebunch wheatgrass | |
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Scientific classification 
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| Kingdom: | Plantae |
| Clade: | Tracheophytes |
| Clade: | Angiosperms |
| Clade: | Monocots |
| Clade: | Commelinids |
| Order: | Poales |
| Family: | Poaceae |
| Genus: | Pseudoroegneria |
| Species: | P. spicata
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| Binomial name | |
| Pseudoroegneria spicata (Pursh) Á.Löve 1980
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| Synonyms[1] | |
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List
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Pseudoroegneria spicata is a species of grass known by the common name bluebunch wheatgrass.[2] This native western North American perennial bunchgrass is also known by the scientific synonyms Elymus spicatus and Agropyron spicatum. The grass can be found in the United States, Canada, and Mexico from Alaska and Yukon south as far as Sonora and Nuevo León.[3][4][5]
Description
Bluebunch wheatgrass can grow up to three feet tall.[6] It can often be distinguished from other bunchgrasses by the awns on its seedheads which stand out at an angle nearly 90 degrees from the stem. It is often bluish. The roots of the grass have a waxy layer that helps it resist desiccation in dry soils.[3] In areas with more moisture the grass may produce rhizomes.[3]
The relationship between the traits and climates of P. spicata is consistent with those of other grass species that also have a summer growing season. Populations of P. spicata from warm, arid environments are often smaller with earlier phenology, narrower leaves, and have greater leaf pubescence. This is in contrast to P. spicata plants from wetter and higher nutrient environments, which tend to be bigger, taller, and have larger leaves.[7]
The stems and leaf sheaths of P. spicata dominate photosynthetic carbon uptake during the late spring and summer seasons. Additionally, bluebunch wheatgrass shows a greater investment of biomass and nutrients in the stems and sheaths, causing an increase in photosynthetic capacity per unit surface area.[8]
Pseudoregneria spicata has extensive drought resistant root systems that can compete with and suppress the spread of exotic weeds.[9] Its roots are also known to have significant responses when they come into contact with the roots of other plants. When plants of the same species that were grown in different sites were planted in pots together, the resulting biomass was 30% more than in pots with plants from the same population or site.[10] Furthermore, the elongation of the roots decreased after contact with roots from another plant from the same population, this was compared to after contact with roots from a plant of a different population. Such behavior suggests that the roots of bluebunch wheatgrass are capable of detection and avoidance mechanisms when exposed to intraspecific plants from the same population.
The roots of this grass are also known to have notable physiological responses to enriched soil patches that are treated with varying solutions of nutrients, most notably nitrogen, potassium, and phosphorus. This exploitation of nutrient-rich soil can affect the nutrient status of the overall plant. In phosphorus enriched environments, the mean root uptake of phosphorus was 5–26% higher compared to roots from control soil patches.[9] Results regarding the nutrient uptake capacities of P. spicata potassium enriched environments indicate no apparent difference between enriched and controlled soil. This is in contrast to the nitrogen enrichment experiment, where mean rates of ammonium uptake increased between 22–88% and mean rates of potassium root uptake were 17–71% higher in soil enriched with 50 μm of nitrogen, the lowest concentration tested in a particular study.[9]
Distribution
Pseudoroegneria spicata is the dominant species of grass among the mountainous regions of the western United States, occurring at elevations that range from 150–3,000 m and where precipitation is 250–500 mm.[7] It occurs in many types of habitat, including sagebrush, forests, woodlands, and grasslands. This grass thrives in sandy and clay rich soils, but is also capable of growing on thin, rocky soils. It does not tolerate soils with high alkalinity, salt, or excessive moisture.[7]
Two subspecies of bluebunch wheatgrass are recognized: P. spicata ssp. spicata and P. spicata ssp. inerme, commonly known as beardless bluebunch wheatgrass.[11] The determining characteristic between the two is the presence of divergent awns, or hair-like projections that extend off a larger structure, such as the lemma or floret. These two subspecies have been known to hybridize.[12]
Pseudoroegneria spicata is most commonly found as a diploid (2n = 14), although autotetraploid forms (4n = 28) have been found in eastern Washington (state) and northern Idaho.[13]
Uses
It is an important forage grass for both livestock and native wildlife in western North America.[3] It is widely used for revegetation of degraded habitat in the region, and cultivars have been developed.[14]
State grass
It is the state grass of Montana, Oregon, and Washington.[citation needed]
The grass is outcompeted by noxious weeds such as diffuse knapweed (Centaurea diffusa) and medusahead (Taeniatherum caput-medusae).[3]
References
- ↑ The Plant List, Elymus spicatus (Pursh) Gould
- ↑ "Pseudoroegneria spicata". Natural Resources Conservation Service PLANTS Database. USDA. https://plants.usda.gov/core/profile?symbol=PSSP6.
- ↑ 3.0 3.1 3.2 3.3 3.4 US Forest Service Fire Ecology
- ↑ Biota of North America Program 2014 state-level distribution map
- ↑ SEINet, Southwestern Biodiversity, Arizona chapter photos, description, distribution map
- ↑ Taylor, Ronald J. (1994) (in en). Sagebrush Country: A Wildflower Sanctuary (rev. ed.). Missoula, MT: Mountain Press Pub. Co. pp. 70. ISBN 0-87842-280-3. OCLC 25708726. https://www.worldcat.org/oclc/25708726.
- ↑ 7.0 7.1 7.2 St. Clair JB, Kilkenny F, Johnson R, Shaw N, Weaver G (2013) Genetic variation in adaptive traits and transfer zones for Pseudoroegneria spicata (bluebunch wheatgrass) in the northwestern United States. Evolutionary Applications 6 (3): 933-948.
- ↑ Caldwell MM, Richards JH, Johnson DA, Nowak RS, Dzurec RS (1981) Coping with Herbivory: Photosynthetic Capacity and Resource Allocation in Two Semiarid Agopyron bunchgrasses. Oecologia 50 (1): 14-24.
- ↑ 9.0 9.1 9.2 Jackson RB, Caldwell MM (1991) Kinetic responses of Pseudoroegneria roots to localized soil enrichment. Plant and Soil 138 (2): 231-238.
- ↑ Yang LX, Callaway R, Atwater DZ (2015) Root contact responses and the positive relationship between intraspecific diversity and ecosystem productivity. AoB Plants 7 (10): 1-8.
- ↑ Carlson JR and Barkworth ME (1997) Elymus wawawaiensis: a species hitherto confused with Pseudoroegneria spicata (Triticeae, Poeaceae). Phytologia 83 (1): 312-330.
- ↑ Daubenmire RF (1939) The taxonomy and ecology of Agopyron spicatum and A. inerme. Bulletin of the Torrey Botanical Club 66 (5): 327-329.
- ↑ Hartung ME (1946) Chromosome numbers in Poa, Agopyron, and Elymus. American Journal of Botany 33 (6): 516-532.
- ↑ Larson, S. R., et al. (2004). Population structure in Pseudoroegneria spicata (Poaceae: Triticeae) modeled by Bayesian clustering of AFLP genotypes. American Journal of Botany 91 1791-1801.
External links
- United States Department of Agriculture Plants Profile
- University of Washington, Washington Burke Museum
Wikidata ☰ Q2827251 entry
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