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      Using Leaf Ecological Stoichiometry to Direct the Management of Ligularia virgaurea on the Northeast Qinghai-Tibetan Plateau

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      Frontiers in Environmental Science
      Frontiers Media SA

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          Abstract

          Leaf ecological stoichiometry not only reflects the plasticity and adaptability, but also the growth of plants within environments where temperature, precipitation, and soil properties vary across an elevation gradient. Ligularia virgaurea (Maxim.) Mattf. ex Rehder & Kobuski — an invasive poisonous plant — is common in the northeast portion of China’s Qinghai-Tibetan Plateau and its presence greatly affects the native ecosystem. Based on L. virgaurea leaf carbon ([C] leaf), nitrogen ([N] leaf) and phosphorus ([P] leaf) concentrations, and their ratios, the species’ coping strategies across an elevation gradient (2,600 m, 3,000 m, and 3,300 m) were identified, and served to inform the development of improved management strategies. Mean [C] leaf, [N] leaf and [P] leaf in L. virgaurea across all elevations were 413.14 g·kg −1, 22.76 g·kg −1, and 1.34 g·kg −1, respectively, while [C] leaf: [N] leaf, [C] leaf: [P] leaf, and [N] leaf: [P] leaf were 18.27, 328.76, and 17.93. With an increase in precipitation and decrease in temperature from 2,600 m to 3,000 m–3,300 m, [C] leaf, [C] leaf: [N] leaf and [C] leaf: [P] leaf of L. virgaurea decreased at first and then increased. The [N] leaf and [P] leaf gradually increased, whereas [N] leaf: [P] leaf showed little change. Although temperature, precipitation and soil water content were the main factors affecting the ecological stoichiometry of L. virgaurea leaves, their roles in influencing leaf elements were different. The [C] leaf was mainly influenced by soil water content, [N] leaf by temperature and soil water content, and [P] leaf by all of them. With potential future climate change in the study area, L. virgaurea may grow faster than at present, although soil P may still be a growth-limiting element. As L. virgaurea can reduce plant diversity and the quality of forage, while increasing biomass, management of L. virgaurea should receive greater attention.

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          Salinity tolerance in halophytes.

          Halophytes, plants that survive to reproduce in environments where the salt concentration is around 200 mm NaCl or more, constitute about 1% of the world's flora. Some halophytes show optimal growth in saline conditions; others grow optimally in the absence of salt. However, the tolerance of all halophytes to salinity relies on controlled uptake and compartmentalization of Na+, K+ and Cl- and the synthesis of organic 'compatible' solutes, even where salt glands are operative. Although there is evidence that different species may utilize different transporters in their accumulation of Na+, in general little is known of the proteins and regulatory networks involved. Consequently, it is not yet possible to assign molecular mechanisms to apparent differences in rates of Na+ and Cl- uptake, in root-to-shoot transport (xylem loading and retrieval), or in net selectivity for K+ over Na+. At the cellular level, H+-ATPases in the plasma membrane and tonoplast, as well as the tonoplast H+-PPiase, provide the trans-membrane proton motive force used by various secondary transporters. The widespread occurrence, taxonomically, of halophytes and the general paucity of information on the molecular regulation of tolerance mechanisms persuade us that research should be concentrated on a number of 'model' species that are representative of the various mechanisms that might be involved in tolerance.
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            Global patterns of plant leaf N and P in relation to temperature and latitude.

            A global data set including 5,087 observations of leaf nitrogen (N) and phosphorus (P) for 1,280 plant species at 452 sites and of associated mean climate indices demonstrates broad biogeographic patterns. In general, leaf N and P decline and the N/P ratio increases toward the equator as average temperature and growing season length increase. These patterns are similar for five dominant plant groups, coniferous trees and four angiosperm groups (grasses, herbs, shrubs, and trees). These results support the hypotheses that (i) leaf N and P increase from the tropics to the cooler and drier midlatitudes because of temperature-related plant physiological stoichiometry and biogeographical gradients in soil substrate age and then plateau or decrease at high latitudes because of cold temperature effects on biogeochemistry and (ii) the N/P ratio increases with mean temperature and toward the equator, because P is a major limiting nutrient in older tropical soils and N is the major limiting nutrient in younger temperate and high-latitude soils.
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              N : P ratios in terrestrial plants: variation and functional significance

              Nitrogen (N) and phosphorus (P) availability limit plant growth in most terrestrial ecosystems. This review examines how variation in the relative availability of N and P, as reflected by N : P ratios of plant biomass, influences vegetation composition and functioning. Plastic responses of plants to N and P supply cause up to 50-fold variation in biomass N : P ratios, associated with differences in root allocation, nutrient uptake, biomass turnover and reproductive output. Optimal N : P ratios - those of plants whose growth is equally limited by N and P - depend on species, growth rate, plant age and plant parts. At vegetation level, N : P ratios <10 and >20 often (not always) correspond to N- and P-limited biomass production, as shown by short-term fertilization experiments; however long-term effects of fertilization or effects on individual species can be different. N : P ratios are on average higher in graminoids than in forbs, and in stress-tolerant species compared with ruderals; they correlate negatively with the maximal relative growth rates of species and with their N-indicator values. At vegetation level, N : P ratios often correlate negatively with biomass production; high N : P ratios promote graminoids and stress tolerators relative to other species, whereas relationships with species richness are not consistent. N : P ratios are influenced by global change, increased atmospheric N deposition, and conservation managment. Contents Summary 243 I Introduction 244 II Variability of N : P ratios in response to nutrient  supply 244 III Critical N : P ratios as indicators of nutrient  limitation 248 IV Interspecific variation in N : P ratios 252 V Vegetation properties in relation to N : P ratios 255 VI Implications of N : P ratios for human impacts  on ecosystems 258 VII Conclusions 259 Acknowledgements 259 References 260.
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                Author and article information

                Journal
                Frontiers in Environmental Science
                Front. Environ. Sci.
                Frontiers Media SA
                2296-665X
                February 1 2022
                February 1 2022
                : 9
                Article
                10.3389/fenvs.2021.805405
                03882d23-5c89-4aa7-92b2-7a64e5bd82ce
                © 2022

                Free to read

                https://creativecommons.org/licenses/by/4.0/

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