Pseudoroegneria spicata

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Bluebunch wheatgrass
Pseudoroegneria spicata 01.jpg
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Monocots
Clade: Commelinids
Order: Poales
Family: Poaceae
Genus: Pseudoroegneria
Species:
P. spicata
Binomial name
Pseudoroegneria spicata
Synonyms [1]
List
  • Agropyron divergens(Steud.) P.Candargy
  • Agropyron divergens(Nees ex Steud.) Vasey
  • Agropyron inerme(Scribn. & J.G.Sm.) Rydb.
  • Agropyron spicatum(Pursh) Scribn. & J.G.Sm.
  • Agropyron vaseyiScribn. & J.G.Sm.
  • Elymus spicatus(Pursh) Gould
  • Elytrigia spicata(Pursh) D.R.Dewey
  • Festuca spicataPursh 1813
  • Roegneria spicata(Pursh) Beetle
  • Schedonorus spicatus(Pursh) Roem. & Schult.
  • Triticum aegilopoidesThurb. ex A.Gray 1863 not Forssk. 1775
  • Triticum divergensSteud.
  • Zeia spicata(Pursh) Lunell

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]

Contents

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 growing in Chelan County, Washington Pseudoroegneria spicata 1.jpg
Pseudoroegneria spicata growing in Chelan County, Washington

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 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]

Related Research Articles

<span class="mw-page-title-main">Root</span> Basal organ of a vascular plant

In vascular plants, the roots are the organs of a plant that are modified to provide anchorage for the plant and take in water and nutrients into the plant body, which allows plants to grow taller and faster. They are most often below the surface of the soil, but roots can also be aerial or aerating, that is, growing up above the ground or especially above water.

<span class="mw-page-title-main">Plant nutrition</span> Study of the chemical elements and compounds necessary for normal plant life

Plant nutrition is the study of the chemical elements and compounds necessary for plant growth and reproduction, plant metabolism and their external supply. In its absence the plant is unable to complete a normal life cycle, or that the element is part of some essential plant constituent or metabolite. This is in accordance with Justus von Liebig’s law of the minimum. The total essential plant nutrients include seventeen different elements: carbon, oxygen and hydrogen which are absorbed from the air, whereas other nutrients including nitrogen are typically obtained from the soil.

<span class="mw-page-title-main">Soil fertility</span> The ability of a soil to sustain agricultural plant growth

Soil fertility refers to the ability of soil to sustain agricultural plant growth, i.e. to provide plant habitat and result in sustained and consistent yields of high quality. It also refers to the soil's ability to supply plant/crop nutrients in the right quantities and qualities over a sustained period of time. A fertile soil has the following properties:

<span class="mw-page-title-main">Arbuscular mycorrhiza</span> Symbiotic penetrative association between a fungus and the roots of a vascular plant

An arbuscular mycorrhiza (AM) is a type of mycorrhiza in which the symbiont fungus penetrates the cortical cells of the roots of a vascular plant forming arbuscules. Arbuscular mycorrhiza is a type of endomycorrhiza along with ericoid mycorrhiza and orchid mycorrhiza .They are characterized by the formation of unique tree-like structures, the arbuscules. In addition, globular storage structures called vesicles are often encountered.

<span class="mw-page-title-main">Serpentine soil</span> Soil type

Serpentine soil is an uncommon soil type produced by weathered ultramafic rock such as peridotite and its metamorphic derivatives such as serpentinite. More precisely, serpentine soil contains minerals of the serpentine subgroup, especially antigorite, lizardite, and chrysotile or white asbestos, all of which are commonly found in ultramafic rocks. The term "serpentine" is commonly used to refer to both the soil type and the mineral group which forms its parent materials.

<span class="mw-page-title-main">Rhizosphere</span> Region of soil or substrate comprising the root microbiome

The rhizosphere is the narrow region of soil or substrate that is directly influenced by root secretions and associated soil microorganisms known as the root microbiome. Soil pores in the rhizosphere can contain many bacteria and other microorganisms that feed on sloughed-off plant cells, termed rhizodeposition, and the proteins and sugars released by roots, termed root exudates. This symbiosis leads to more complex interactions, influencing plant growth and competition for resources. Much of the nutrient cycling and disease suppression by antibiotics required by plants, occurs immediately adjacent to roots due to root exudates and metabolic products of symbiotic and pathogenic communities of microorganisms. The rhizosphere also provides space to produce allelochemicals to control neighbours and relatives.

Claypan is a dense, compact, slowly permeable layer in the subsoil. It has a much higher clay content than the overlying material, from which it is separated by a sharply defined boundary. The dense structure restricts root growth and water infiltration. Therefore, a perched water table might form on top of the claypan. In the Canadian classification system, claypan is defined as a clay-enriched illuvial B (Bt) horizon.

<span class="mw-page-title-main">Soil respiration</span> Chemical process produced by soil and the organisms within it

Soil respiration refers to the production of carbon dioxide when soil organisms respire. This includes respiration of plant roots, the rhizosphere, microbes and fauna.

<i>Elymus elymoides</i> Species of flowering plant

Elymus elymoides is a species of wild rye known by the common name squirreltail. This grass is native to most of North America west of the Mississippi River and occurs in a number of ecosystems, from the alpine zone to desert sage scrub to valley grassland.

Microbial inoculants also known as soil inoculants or bioinoculants are agricultural amendments that use beneficial rhizosphericic or endophytic microbes to promote plant health. Many of the microbes involved form symbiotic relationships with the target crops where both parties benefit (mutualism). While microbial inoculants are applied to improve plant nutrition, they can also be used to promote plant growth by stimulating plant hormone production. Although bacterial and fungal inoculants are common, inoculation with archaea to promote plant growth is being increasingly studied.

<i>Leymus arenarius</i> Species of flowering plant in the grass family Poaceae

Leymus arenarius is a psammophilic (sand-loving) species of grass in the family Poaceae, native to the coasts of Atlantic and Northern Europe. Leymus arenarius is commonly known as sand ryegrass, sea lyme grass, or simply lyme grass.

<span class="mw-page-title-main">Phosphorus deficiency</span>

Phosphorus deficiency is a plant disorder associated with insufficient supply of phosphorus. Phosphorus refers here to salts of phosphates (PO43−), monohydrogen phosphate (HPO42−), and dihydrogen phosphate (H2PO4). These anions readily interconvert, and the predominant species is determined by the pH of the solution or soil. Phosphates are required for the biosynthesis of genetic material as well as ATP, essential for life. Phosphorus deficiency can be controlled by applying sources of phosphorus such as bone meal, rock phosphate, manure, and phosphate-fertilizers.

<span class="mw-page-title-main">Biofertilizer</span> Substance with micro-organisms

A biofertilizer is a substance which contains living micro-organisms which, when applied to seeds, plant surfaces, or soil, colonize the rhizosphere or the interior of the plant and promotes growth by increasing the supply or availability of primary nutrients to the host plant. Biofertilizers add nutrients through the natural processes of nitrogen fixation, solubilizing phosphorus, and stimulating plant growth through the synthesis of growth-promoting substances. The micro-organisms in biofertilizers restore the soil's natural nutrient cycle and build soil organic matter. Through the use of biofertilizers, healthy plants can be grown, while enhancing the sustainability and the health of the soil. Biofertilizers can be expected to reduce the use of synthetic fertilizers and pesticides, but they are not yet able to replace their use. Since they play several roles, a preferred scientific term for such beneficial bacteria is "plant-growth promoting rhizobacteria" (PGPR).

<span class="mw-page-title-main">Hartig net</span> Network of inward-growing hyphae

The Hartig net is the network of inward-growing hyphae, that extends into the plant host root, penetrating between plant cells in the root epidermis and cortex in ectomycorrhizal symbiosis. This network is the internal component of fungal morphology in ectomycorrhizal symbiotic structures formed with host plant roots, in addition to a hyphal mantle or sheath on the root surface, and extramatrical mycelium extending from the mantle into the surrounding soil. The Hartig net is the site of mutualistic resource exchange between the fungus and the host plant. Essential nutrients for plant growth are acquired from the soil by exploration and foraging of the extramatrical mycelium, then transported through the hyphal network across the mantle and into the Hartig net, where they are released by the fungi into the root apoplastic space for uptake by the plant. The hyphae in the Hartig net acquire sugars from the plant root, which are transported to the external mycelium to provide a carbon source to sustain fungal growth.

<i>Elymus lanceolatus</i> Species of grass

Elymus lanceolatus is a species of grass known by the common names thickspike wheatgrass and streamside wheatgrass. It is native to North America, where it is widespread and abundant in much of Canada and the western and central United States. There are two subspecies, subsp. lanceolatus occurring throughout the species' range and subsp. psammophilus occurring in the Great Lakes region.

<i>Elymus hoffmannii</i> Species of grass

Elymus hoffmannii is a species of grass known by the common name RS wheatgrass. It was described as a new species in 1996. It became known to science when some grasses were collected in Turkey in 1979 and one type was successfully bred out, proving to be a natural hybrid. E. hoffmannii is derived from this hybrid between Elymus repens and the bluebunch wheatgrasses of Turkey, such as Pseudoroegneria spicata.

<i>Elymus wawawaiensis</i> Species of flowering plant

Elymus wawawaiensis is a species of grass known by the common name Snake River wheatgrass. It is native to western North America, where it occurs in the Pacific Northwest. It is native to eastern Washington and Oregon and parts of Idaho.

Biomass partitioning is the process by which plants divide their energy among their leaves, stems, roots, and reproductive parts. These four main components of the plant have important morphological roles: leaves take in CO2 and energy from the sun to create carbon compounds, stems grow above competitors to reach sunlight, roots absorb water and mineral nutrients from the soil while anchoring the plant, and reproductive parts facilitate the continuation of species. Plants partition biomass in response to limits or excesses in resources like sunlight, carbon dioxide, mineral nutrients, and water and growth is regulated by a constant balance between the partitioning of biomass between plant parts. An equilibrium between root and shoot growth occurs because roots need carbon compounds from photosynthesis in the shoot and shoots need nitrogen absorbed from the soil by roots. Allocation of biomass is put towards the limit to growth; a limit below ground will focus biomass to the roots and a limit above ground will favor more growth in the shoot.

Some types of lichen are able to fix nitrogen from the atmosphere. This process relies on the presence of cyanobacteria as a partner species within the lichen. The ability to fix nitrogen enables lichen to live in nutrient-poor environments. Lichen can also extract nitrogen from the rocks on which they grow.

Seventeen elements or nutrients are essential for plant growth and reproduction. They are carbon (C), hydrogen (H), oxygen (O), nitrogen (N), phosphorus (P), potassium (K), sulfur (S), calcium (Ca), magnesium (Mg), iron (Fe), boron (B), manganese (Mn), copper (Cu), zinc (Zn), molybdenum (Mo), nickel (Ni) and chlorine (Cl). Nutrients required for plants to complete their life cycle are considered essential nutrients. Nutrients that enhance the growth of plants but are not necessary to complete the plant's life cycle are considered non-essential, although some of them, such as silicon (Si), have been shown to improve nutrent availability, hence the use of stinging nettle and horsetail macerations in Biodynamic agriculture. With the exception of carbon, hydrogen and oxygen, which are supplied by carbon dioxide and water, and nitrogen, provided through nitrogen fixation, the nutrients derive originally from the mineral component of the soil. The Law of the Minimum expresses that when the available form of a nutrient is not in enough proportion in the soil solution, then other nutrients cannot be taken up at an optimum rate by a plant. A particular nutrient ratio of the soil solution is thus mandatory for optimizing plant growth, a value which might differ from nutrient ratios calculated from plant composition.

References

  1. The Plant List, Elymus spicatus (Pursh) Gould
  2. USDA, NRCS (n.d.). "Pseudoroegneria spicata". The PLANTS Database (plants.usda.gov). Greensboro, North Carolina: National Plant Data Team. Retrieved 15 October 2015.
  3. 1 2 3 4 5 US Forest Service Fire Ecology
  4. Biota of North America Program 2014 state-level distribution map
  5. SEINet, Southwestern Biodiversity, Arizona chapter photos, description, distribution map
  6. Taylor, Ronald J. (1994) [1992]. Sagebrush Country: A Wildflower Sanctuary (rev. ed.). Missoula, MT: Mountain Press Pub. Co. p. 70. ISBN   0-87842-280-3. OCLC   25708726.
  7. 1 2 3 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.
  8. 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. 1 2 3 Jackson RB, Caldwell MM (1991) Kinetic responses of Pseudoroegneria roots to localized soil enrichment. Plant and Soil 138 (2): 231-238.
  10. 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.
  11. Carlson JR and Barkworth ME (1997) Elymus wawawaiensis: a species hitherto confused with Pseudoroegneria spicata (Triticeae, Poeaceae). Phytologia 83 (1): 312-330.
  12. Daubenmire RF (1939) The taxonomy and ecology of Agopyron spicatum and A. inerme. Bulletin of the Torrey Botanical Club 66 (5): 327-329.
  13. Hartung ME (1946) Chromosome numbers in Poa, Agopyron, and Elymus. American Journal of Botany 33 (6): 516-532.
  14. 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.