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Invasive Forb, Annual Grass, and Exotic Shrub Competition with Three Sagebrush-Steppe Growth Forms: Acquisition of a Spring 15N Tracer
- Eamonn D. Leonard, Thomas A. Monaco, John M. Stark, Ron J. Ryel
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- Journal:
- Invasive Plant Science and Management / Volume 1 / Issue 2 / April 2008
- Published online by Cambridge University Press:
- 20 January 2017, pp. 168-177
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Understanding competition for soil nitrate between common shrub-steppe, potential reclamation species, and common invasive species is necessary to identify mechanisms associated with ecosystem invasion and can assist with developing weed management scenarios. We designed a field experiment to evaluate the differential competitive effects of the invasive annual grass downy brome, the invasive biennial forb dyer's woad, and the reclamation shrub prostrate kochia, on nitrate acquisition of the perennial grass crested wheatgrass, the native forb western yarrow, and the native shrub big sagebrush. Individual plants were grown in two-plant neighborhoods, and a K15NO3 tracer was injected into the soil between plants and recovered from leaf material after 5 to 11 d. We also evaluated neighbor effects on shoot and root growth, leaf carbon : nitrogen ratio, and leaf nitrogen concentrations to better understand how these traits are associated with differences in nitrate acquisition and nitrogen allocation among the three growth forms. Nitrate acquisitions by crested wheatgrass and western yarrow were significantly lower when competing with downy brome than with dyer's woad and prostrate kochia; however, competitors had similar, negative effects on nitrate acquisition by big sagebrush. Nitrate acquisition ratios between competing neighbors revealed that: (1) the grasses always acquired more nitrate than neighbors of a different growth form, (2) western yarrow was equally competitive with dyer's woad and prostrate kochia, and (3) all neighbors acquired more nitrate than big sagebrush. More successful competition for nitrate in the grasses was associated with greater specific root length. Compared to species of the same respective growth form, the two invasive weeds (downy brome and dyer's woad) and prostrate kochia always had significantly lower leaf carbon : nitrogen ratio, and greater leaf nitrogen concentration, which have been broadly correlated with leaf lifespan and nutrient use efficiency, and indicate differing strategies to persist in the semiarid shrub-steppe ecosystems.
Comparison of root and mycorrhizal characteristics in primary and secondary rainforest on a metamorphic soil in North Queensland, Australia
- Michael S. Hopkins, Paul Reddell, Robert K. Hewett, Andrew W. Graham
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- Journal:
- Journal of Tropical Ecology / Volume 12 / Issue 6 / November 1996
- Published online by Cambridge University Press:
- 10 July 2009, pp. 871-885
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Root biomass, root lengths, and mycorrhizal associations were compared in a series of primary and Acacia-dominated secondary rainforest stands on nutrient-poor, red podzolic soils developed from low grade Palaeozoic metasediments. Five soil cores to 200 mm depth were collected at random locations from each of 20 sites. Ten of these sites were in 20–25 m high closed secondary forest (30–40 y old) dominated by Acacia aulacocarpa and ten sites were located in primary, selectively-logged, rainforest (28–32 m tall). Arbuscular mycorrhizas were the only form of association found in the primary forest sites. Ectomycorrhizas dominated the secondary forest sites although arbuscular mycorrhizas were also present. The primary forest sites had significantly higher root biomass (34.4 ± 17.8 t ha-1) and root length (33,400 ± 3,200 km ha-1) than the secondary forests (11.6 ± 4.6 t ha-1 and 25,200 ± 4,800 km ha-1 respectively), and this was interpreted as a reflection of the greater allocation of biomass to roots necessary to support the greater above ground biomass. The specific root length in the secondary forest (340 ± 119 cm g-1) was twice that of the primary forest (154 ± 65 cm g-1) indicating that the trees in the secondary forests achieved a degree of soil exploration which was comparable to that in the primary forest with less than half the biomass allocation to roots. The dominance of ectomycorrhizas in the secondary forest was associated with the prevalence of Acacia aulacocarpa, and the results cannot be extended to other secondary forests in the region. The implications that the dominant ectomycorrhizal associations have for the patterns of successional development and the patterns of species colonization in these Acaria-dominated secondary forests are discussed.
Building roots in a changing environment: implications for root longevity
- D. M. EISSENSTAT, C. E. WELLS, R. D. YANAI, J. L. WHITBECK
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- Journal:
- The New Phytologist / Volume 147 / Issue 1 / July 2000
- Published online by Cambridge University Press:
- 01 July 2000, pp. 33-42
- Print publication:
- July 2000
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Root turnover is important to the global carbon budget as well as to nutrient cycling in ecosystems and to the success of individual plants. Our ability to predict the effects of environmental change on root turnover is limited by the difficulty of measuring root dynamics, but emerging evidence suggests that roots, like leaves, possess suites of interrelated traits that are linked to their life span. In graminoids, high tissue density has been linked to increased root longevity. Other studies have found root longevity to be positively correlated with mycorrhizal colonization and negatively correlated with nitrogen concentration, root maintenance respiration and specific root length. Among fruit trees, apple roots (which are of relatively small diameter, low tissue density and have little lignification of the exodermis) have much shorter life spans than the roots of citrus, which have opposite traits. Likewise, within the branched network of the fine root system, the finest roots with no daughter roots tend to have higher N concentrations, faster maintenance respiration, higher specific root length and shorter life spans than secondary and tertiary roots that bear daughter roots. Mycorrhizal colonization can enhance root longevity by diverse mechanisms, including enhanced tolerance of drying soil and enhanced defence against root pathogens. Many variables involved in building roots might affect root longevity, including root diameter, tissue density, N concentration, mycorrhizal fungal colonization and accumulation of secondary phenolic compounds. These root traits are highly plastic and are strongly affected by resource supply (CO2, N, P and water). Therefore the response of root longevity to altered resource availability associated with climate change can be estimated by considering how changes in resource availability affect root construction and physiology. A cost–benefit approach to predicting root longevity assumes that a plant maintains a root only until the efficiency of resource acquisition is maximized. Using an efficiency model, we show that reduced tissue Nconcentration and reduced root maintenance respiration, both of which are predicted to result from elevated CO2, should lead to slightly longer root life spans. Complex interactions with soil biota and shifts in plant defences against root herbivory and parasitism, which are not included in the present efficiency model, might alter the effects of future climate change on root longevity in unpredicted ways.