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      Seasonal Dynamics of Mobile Carbon Supply in Quercus aquifolioides at the Upper Elevational Limit

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          Abstract

          Many studies have tried to explain the physiological mechanisms of the alpine treeline phenomenon, but the debate on the alpine treeline formation remains controversial due to opposite results from different studies. The present study explored the carbon-physiology of an alpine shrub species ( Quercus aquifolioides) grown at its upper elevational limit compared to lower elevations, to test whether the elevational limit of alpine shrubs (<3 m in height) are determined by carbon limitation or growth limitation. We studied the seasonal variations in non-structural carbohydrate (NSC) and its pool size in Q. aquifolioides grown at 3000 m, 3500 m, and at its elevational limit of 3950 m above sea level (a.s.l.) on Zheduo Mt., SW China. The tissue NSC concentrations along the elevational gradient varied significantly with season, reflecting the season-dependent carbon balance. The NSC levels in tissues were lowest at the beginning of the growing season, indicating that plants used the winter reserve storage for re-growth in the early spring. During the growing season, plants grown at the elevational limit did not show lower NSC concentrations compared to plants at lower elevations, but during the winter season, storage tissues, especially roots, had significantly lower NSC concentrations in plants at the elevational limit compared to lower elevations. The present results suggest the significance of winter reserve in storage tissues, which may determine the winter survival and early-spring re-growth of Q. aquifolioides shrubs at high elevation, leading to the formation of the uppermost distribution limit. This result is consistent with a recent hypothesis for the alpine treeline formation.

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          Carbohydrate sources and sinks in woody plants

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            Cloud cover limits net CO2 uptake and growth of a rainforest tree during tropical rainy seasons.

            Recent global-scale analyses indicate that climate variability affects net carbon storage but regard temperature and precipitation to be the main contributors. Seasonal and interannual variation in light availability may also limit CO(2) uptake. As an experimental test of light limitation by cloud cover during tropical rainy seasons and by the unusually heavy cloud cover associated with La Niña, we installed high-intensity lamps above the forest canopy to augment light for Luehea seemannii, a tropical canopy tree species, during cloudy periods of 1999-2000. Light augmentation only partially compensated for the reduction in photosynthetic photon flux density caused by clouds. Nonetheless, leaves acclimated to the augmented irradiance, and photosynthesis, vegetative growth, and reproduction increased significantly. Light, rather than water, temperature, or leaf nitrogen, was the primary factor limiting CO(2) uptake during the rainy season.
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              Contrasting distribution and seasonal dynamics of carbohydrate reserves in stem wood of adult ring-porous sessile oak and diffuse-porous beech trees.

              We tested the hypothesis that broad-leaved forest species with contrasting wood anatomy and hydraulic system (ring-porous versus diffuse-porous) also differ in distribution and seasonal dynamics of carbohydrate reserves in stem wood. Total nonstructural carbohydrate (TNC) reserves (starch and sugars) were measured enzymatically in the 10 youngest stem xylem rings of adult oak (Quercus petraea (Matt.) Liebl.) and beech (Fagus sylvatica L.) trees during an annual cycle. Radial distribution of carbohydrates was investigated according to ring age. On all dates, oak trees had twofold higher TNC concentration than beech trees (41 versus 23 mg g(DM)(-1)), with starch accounting for the high TNC concentration in oak. Seasonal dynamics of TNC concentration were significantly (P < 0.05) more pronounced in oak (20-64 mg TNC g(DM)(-1)) than in beech (17-34 mg TNC g(DM)(-1)). A marked decrease in TNC concentration was observed in oak trees during bud burst and early wood growth, whereas seasonal fluctuations in TNC concentrations in beech trees were small. The radial distribution of TNC based on ring age differed between species: TNC was restricted to the sapwood rings in oak, whereas in beech, it was distributed throughout the wood from the outermost sapwood ring to the pith. Although the high TNC concentrations in the outermost rings accounted for most of the observed seasonal pattern, all of the 10 youngest xylem rings analyzed participated in the seasonal dynamics of TNC in beech trees. The innermost sapwood rings of oak trees had low TNC concentrations. Stem growth and accumulation of carbon reserves occurred concomitantly during the first part of the season, when there was no soil water deficit. When soil water content was depleted, stem growth ceased in both species, whereas TNC accumulation was negligibly affected and continued until leaf fall. The contrasting dynamics and distribution of carbohydrate reserves in oak and beech are discussed with reference to differences in phenology, early spring growth and hydraulic properties between ring-porous trees and diffuse-porous trees.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2012
                30 March 2012
                : 7
                : 3
                : e34213
                Affiliations
                [1 ]Alpine Ecosystem Observation and Experiment Station of Gongga Mountain, Institute of Mountain Hazard and Environment, Chinese Academy of Sciences, Chengdu, China
                [2 ]Tree Physiology Group, Swiss Federal Research Institute WSL, Birmensdorf, Switzerland
                [3 ]State Key Laboratory of Forest and Soil Ecology, Institute of Applied Ecology, Chinese Academy of Sciences, Shenyang, China
                [4 ]Key Laboratory of Tropical Forest Ecology, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Mengla, China
                [5 ]College of Agronomy and Biotechnology, Southwest University, Chongqing, China
                [6 ]Key Laboratory of Forest Ecology and Environment, State Forestry Administration, Chinese Academy of Forestry, Beijing, China
                Ohio State University, United States of America
                Author notes

                Conceived and designed the experiments: WZZ MHL. Performed the experiments: WZZ MC WFX SGW. Analyzed the data: WZZ MHL. Contributed reagents/materials/analysis tools: SGW. Wrote the paper: WZZ MHL.

                Article
                PONE-D-11-21637
                10.1371/journal.pone.0034213
                3316670
                22479567
                9f611906-647a-4388-949d-24c1432804e3
                Zhu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 29 October 2011
                : 28 February 2012
                Page count
                Pages: 11
                Categories
                Research Article
                Agriculture
                Forestry
                Biology
                Ecology
                Plant Ecology
                Plant Science
                Plant Ecology
                Earth Sciences
                Geochemistry

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                Uncategorized

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