» Articles » PMID: 28312969

The Population Biology of Bromus Tectorum in Forests: Distinguishing the Opportunity for Dispersal from Environmental Restriction

Overview
Journal Oecologia
Date 2017 Mar 18
PMID 28312969
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

With increasing elevation and corresponding changes in the macroclimate, forest zones in the Intermountain Region of western North America are often dominated in turn by Pinus ponderosa, Pseudotsuga menziesii, Abies grandis, an Thuja plicata. Bromus tectorum (cheatgrass), and introduced annual grass now abundant in the Region's steppe, is uncommon in mature stands representative of these forest zones. In order to determine whether B. tectorum is largely excluded from these forests by insufficient seed dispersal or environmental restriction(s), the grass's demography was compared in each of four years among populations experimentally-introduced into mature forests. The number of recruits did not differ among the Pinus, Pseudotsuga, and Abies sites; recruitment was however significantly lower on the coolest site dominated by Thuja. Emergence in both the low elevation Pinus and Pseudotsuga sites was about the same in autumn, winter, and spring. In the cooler, moister Abies and Thuja sites, emergence was limited to autumn and early winter. Survival in these forest sites ranged between 0 and 87%. The percentage of the total population to survive until harvest was highest in the Pseudotsuga site, intermediate in the Pinus and Abies sites, and lowest in the Thuja site. Compared with B. tectorum in the steppe, the surviving plants were small, and few produced seeds. All parents were members of either the autumn or winter cohort, and most parents produced only one seed. No seeds were produced at the Thuja site. Although phenotypic plasticity apparently contributes to the wide ecological amplitude of this grass, its growing season on these sites in most years is too short for it to reproduce. Consequently, these forest zones broadly define the current environmental limits to the distribution of cheatgrass in this portion of its new geographic range.

Citing Articles

Plant and soil microbial composition legacies following indaziflam herbicide treatment.

Bradbury E, Holland-Moritz H, Gill A, Havrilla C Front Microbiol. 2025; 15:1450633.

PMID: 39744400 PMC: 11688475. DOI: 10.3389/fmicb.2024.1450633.


Genetic analysis of Bromus tectorum (Poaceae) in the Mediterranean region: biogeographical pattern of native populations.

Kelly L, Mack R, Novak S Heredity (Edinb). 2020; 126(1):178-193.

PMID: 32814871 PMC: 7853138. DOI: 10.1038/s41437-020-00354-0.


The effect of shading on photosynthesis, growth, and regrowth following defoliation for Bromus tectorum.

Pierson E, Mack R, Black R Oecologia. 2017; 84(4):534-543.

PMID: 28312971 DOI: 10.1007/BF00328171.


The population biology of Bromus tectorum in forests: effect of disturbance, grazing, and litter on seedling establishment and reproduction.

Pierson E, Mack R Oecologia. 2017; 84(4):526-533.

PMID: 28312970 DOI: 10.1007/BF00328170.


Ecological genetics of Bromus tectorum : III. The demography of reciprocally sown populations.

Rice K, Mack R Oecologia. 2017; 88(1):91-101.

PMID: 28312736 DOI: 10.1007/BF00328408.


References
1.
Bookman P . Microsite utilization by Bromus tectorum L. and Poa pratensis L. in a meadow steppe community. Oecologia. 2017; 56(2-3):413-418. DOI: 10.1007/BF00379721. View

2.
Pierson E, Mack R, Black R . The effect of shading on photosynthesis, growth, and regrowth following defoliation for Bromus tectorum. Oecologia. 2017; 84(4):534-543. DOI: 10.1007/BF00328171. View

3.
Lande R . Genetics and demography in biological conservation. Science. 1988; 241(4872):1455-60. DOI: 10.1126/science.3420403. View